Mechanism of aggregation of UV-irradiated glycogen phosphorylase b at a low temperature in the presence of crowders and trimethylamine N-oxide

To characterize the initial stages of protein aggregation, the kinetics of aggregation of UV-irradiated glycogen phosphorylase b (UV-Phb) was studied under conditions when the aggregation proceeded at a low rate (10°C, 0.03M Hepes buffer, pH6.8, containing 0.1M NaCl). Aggregation of UV-Phb was induc...

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Published in:Biophysical chemistry Vol. 232; pp. 12 - 21
Main Authors: Eronina, Tatiana B., Mikhaylova, Valeriya V., Chebotareva, Natalia A., Borzova, Vera A., Yudin, Igor K., Kurganov, Boris I.
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 01-01-2018
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Abstract To characterize the initial stages of protein aggregation, the kinetics of aggregation of UV-irradiated glycogen phosphorylase b (UV-Phb) was studied under conditions when the aggregation proceeded at a low rate (10°C, 0.03M Hepes buffer, pH6.8, containing 0.1M NaCl). Aggregation of UV-Phb was induced by polyethylene glycol and Ficoll-70, acting as crowders, or a natural osmolyte trimethylamine N-oxide (TMAO). It has been shown that the initial rate of the stage of aggregate growth is proportional to the protein concentration squared, suggesting that the order of aggregation with respect to the protein is equal to two. It has been concluded that the aggregation mechanism of UV-Phb at 10°C in the presence of crowders includes the nucleation stage and stages of protein aggregate growth (the basic aggregation pathway). The aggregation mechanism is complicated in the presence of TMAO, and the stage of aggregate-aggregate assembly induced by TMAO should be added to the basic aggregation pathway. It has been shown that the ability of TMAO at a low concentration (0.05M) to induce aggregation of UV-Phb is due to the decrease in the absolute value of zeta potential of the protein in the presence of TMAO. [Display omitted] •Kinetic regime of aggregation of UV-irradiated glycogen phosphorylase b at 10°C has been established.•Crowders (Ficoll-70 and polyethylene glycol) and osmolyte trimethylamine N-oxide (TMAO) stimulate protein aggregation.•The initial rate of the stage of aggregate growth is proportional to the protein concentration squared.•In contrast to crowders, TMAO induces sticking of the aggregates formed in the aggregation process.
AbstractList To characterize the initial stages of protein aggregation, the kinetics of aggregation of UV-irradiated glycogen phosphorylase b (UV-Phb) was studied under conditions when the aggregation proceeded at a low rate (10°C, 0.03M Hepes buffer, pH6.8, containing 0.1M NaCl). Aggregation of UV-Phb was induced by polyethylene glycol and Ficoll-70, acting as crowders, or a natural osmolyte trimethylamine N-oxide (TMAO). It has been shown that the initial rate of the stage of aggregate growth is proportional to the protein concentration squared, suggesting that the order of aggregation with respect to the protein is equal to two. It has been concluded that the aggregation mechanism of UV-Phb at 10°C in the presence of crowders includes the nucleation stage and stages of protein aggregate growth (the basic aggregation pathway). The aggregation mechanism is complicated in the presence of TMAO, and the stage of aggregate-aggregate assembly induced by TMAO should be added to the basic aggregation pathway. It has been shown that the ability of TMAO at a low concentration (0.05M) to induce aggregation of UV-Phb is due to the decrease in the absolute value of zeta potential of the protein in the presence of TMAO. [Display omitted] •Kinetic regime of aggregation of UV-irradiated glycogen phosphorylase b at 10°C has been established.•Crowders (Ficoll-70 and polyethylene glycol) and osmolyte trimethylamine N-oxide (TMAO) stimulate protein aggregation.•The initial rate of the stage of aggregate growth is proportional to the protein concentration squared.•In contrast to crowders, TMAO induces sticking of the aggregates formed in the aggregation process.
To characterize the initial stages of protein aggregation, the kinetics of aggregation of UV-irradiated glycogen phosphorylase b (UV-Phb) was studied under conditions when the aggregation proceeded at a low rate (10°C, 0.03M Hepes buffer, pH6.8, containing 0.1M NaCl). Aggregation of UV-Phb was induced by polyethylene glycol and Ficoll-70, acting as crowders, or a natural osmolyte trimethylamine N-oxide (TMAO). It has been shown that the initial rate of the stage of aggregate growth is proportional to the protein concentration squared, suggesting that the order of aggregation with respect to the protein is equal to two. It has been concluded that the aggregation mechanism of UV-Phb at 10°C in the presence of crowders includes the nucleation stage and stages of protein aggregate growth (the basic aggregation pathway). The aggregation mechanism is complicated in the presence of TMAO, and the stage of aggregate-aggregate assembly induced by TMAO should be added to the basic aggregation pathway. It has been shown that the ability of TMAO at a low concentration (0.05M) to induce aggregation of UV-Phb is due to the decrease in the absolute value of zeta potential of the protein in the presence of TMAO.
Author Mikhaylova, Valeriya V.
Yudin, Igor K.
Kurganov, Boris I.
Borzova, Vera A.
Eronina, Tatiana B.
Chebotareva, Natalia A.
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  givenname: Vera A.
  surname: Borzova
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  surname: Kurganov
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  organization: Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, 33, bld. 2, Leninsky Ave., Moscow 119071, Russia
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Cites_doi 10.1016/0092-8674(82)90231-8
10.1038/425027a
10.1016/S0301-4622(03)00134-0
10.1016/S1570-9639(03)00167-5
10.1110/ps.29301
10.1021/j150512a005
10.1007/s10541-005-0219-8
10.1046/j.1432-1327.2001.01838.x
10.1016/bs.ircmb.2016.08.014
10.1515/BC.2006.064
10.1016/0301-4622(95)00044-X
10.1016/j.ijbiomac.2013.05.010
10.1134/S000629790603014X
10.1074/jbc.R100005200
10.1103/PhysRevLett.93.228104
10.1111/j.1742-4658.2005.04696.x
10.1007/3-540-44672-9_11
10.1016/j.ijbiomac.2016.02.010
10.1021/jp304298c
10.1016/j.bbapap.2006.08.012
10.1016/j.bpc.2008.12.007
10.1023/A:1015589926728
10.1016/0003-9861(92)90550-G
10.1016/j.ijbiomac.2015.07.002
10.1023/A:1015277805345
10.1134/S0006297909050125
10.1007/s10541-005-0070-y
10.1021/bi00850a037
10.1073/pnas.0606236103
10.1016/j.bpc.2011.04.011
10.1016/j.ijbiomac.2015.06.040
10.1021/bi201030y
10.1016/j.ijbiomac.2016.05.080
10.4172/2161-1009.1000e138
10.1146/annurev.bb.22.060193.000331
10.1074/jbc.M410716200
10.1016/j.biochi.2014.11.001
10.1146/annurev-biophys-062215-011236
10.1002/bip.360331012
10.1016/S0968-0004(01)01938-7
10.3390/ijms151223090
10.1007/s12551-016-0220-z
10.1074/jbc.274.46.32970
10.1021/bi1018368
10.1073/pnas.71.12.4864
10.1134/S0006297907130056
10.1016/j.ijbiomac.2016.07.066
10.1016/j.ijbiomac.2016.08.038
10.1073/pnas.122225399
10.1002/mabi.200900397
10.1242/jeb.01730
10.1146/annurev.biophys.37.032807.125817
10.1073/pnas.79.23.7107
10.1021/bi8008399
10.1002/bit.21627
10.1016/j.ijbiomac.2015.02.022
10.1021/jp207289b
10.1146/annurev.biophys.30.1.271
10.1038/s41598-017-04409-x
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Keywords Kinetic regime
Protein aggregation
Glycogen phosphorylase b
Crowding
Language English
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References Chebotareva, Eronina, Roman, Poliansky, Muranov, Kurganov (bb0050) 2013; 60
Kastenschmidt, Kastenschmidt, Helmreich (bb0235) 1968; 7
Roman, Chebotareva, Eronina, Kleymenov, Makeeva, Poliansky, Muranov, Kurganov (bb0095) 2011; 50
Roman, Chebotareva, Kurganov (bb0100) 2017; 100
Ellis, Minton (bb0065) 2006; 387
Lumry, Erying (bb0325) 1954; 58
Chebotareva, Harding, Winzor (bb0030) 2001; 268
Borwankar, Röthlein, Zhang, Techen, Dosche, Ignatova (bb0180) 2011; 50
Minton, Karmin, Hahn, Minton (bb0330) 1982; 79
Eronina, Chebotareva, Bazhina, Makeeva, Kleymenov, Kurganov (bb0230) 2009; 141
Ellis, Minton (bb0020) 2003; 425
Wang, Kurganov (bb0270) 2003; 106
Chebotareva, Eronina, Sluchanko, Kurganov (bb0060) 2015; 76
Kuznetsova, Turoverov, Uversky (bb0080) 2014; 15
Yancey (bb0195) 2005; 208
Kurganov (bb0280) 2017; 100
Ali, Manzoor, Azam, Ansari (bb0145) 2012
Canchi, Jayasimha, Rau, Makhatadze, Garcia (bb0165) 2012; 116
Fedurkina, Belousova, Mitskevich, Zhou, Chang, Kurganov (bb0305) 2006; 71
Kurganov (bb0275) 2005; vol. 2
Kurganov (bb0265) 2002; 42
Chebotareva (bb0040) 2007; 72
Hall, Minton (bb0025) 2003; 1649
Chebotareva, Kurganov, Livanova (bb0035) 2004; 69
Kurganov (bb0260) 2002; 67
Timasheff (bb0190) 2002; 99
Roberts (bb0240) 2006
Chandel, Khan, Khan (bb0150) 2012
Ellis (bb0070) 2011
Davis-Searles, Saunders, Erie, Winzor, Pielak (bb0215) 2001; 30
Gruebele, Dave, Sukenik (bb0075) 2016; 45
Minton (bb0085) 2001; 276
Ellis (bb0015) 2001; 26
Buell (bb0250) 2017; 329
Singh, Haque, Ahmad (bb0170) 2005; 280
Wills, Winzor (bb0115) 2011; 158
Arakawa, Ejima, Kita, Tsumoto (bb0185) 2006; 1764
Hill (bb0315) 1986
Fulton (bb0005) 1982; 30
Mukherjee, Santra, Beuria, Panda (bb0130) 2005; 272
Roberts (bb0245) 2007; 98
Street, Bolen, Rose (bb0200) 2006; 103
Eronina, Mikhaylova, Chebotareva, Makeeva, Kurganov (bb0225) 2016; 86
Cho, Reddy, Straub, Thirumalai (bb0160) 2011; 115
Winzor, Winzor, Paleg, Jones, Naidu (bb0335) 1992; 296
Wills, Winzor (bb0210) 1993; 33
(bb0290) 1995
Zimmerman, Minton (bb0010) 1993; 22
Sluchanko, Chebotareva, Gusev (bb0105) 2015; 108
Samiotakis, Wittung-Stafshede, Cheung (bb0110) 2009; 10
Yang, Yip, Huangi, Chakrabarttyi, Fraser (bb0175) 1999; 274
Chebotareva, Meremyanin, Makeeva, Eronina, Kurganov (bb0155) 2009; 74
Despa, Fernandez, Berry (bb0205) 2004; 93
Eronina, Mikhaylova, Chebotareva, Kurganov (bb0285) 2016; 92
Weatherly, Pielak (bb0220) 2001; 10
Borzova, Markossian, Kara, Kurganov (bb0345) 2015; 80
Chebotareva, Roman, Kurganov (bb0140) 2016; 8
Zhou, Rivas, Minton (bb0125) 2008; 37
Kurganov, Chebotareva (bb0120) 2013; 2
Chebotareva, Filippov, Kurganov (bb0055) 2015; 80
Hall, Jacobsen, Winzor (bb0340) 1995; 57
Munishkina, Ahmad, Fink, Uversky (bb0090) 2008; 47
Hofrichter, Ross, Eaton (bb0255) 1974; 71
Chebotareva, Makeeva, Bazhina, Eronina, Gusev, Kurganov (bb0045) 2010; 10
Kurganov, Rafikova, Dobrov (bb0300) 2002; 67
Chebotareva, Andreeva, Makeeva, Kurganov, Livanova, Harding (bb0310) 2002; 119
Eronina, Chebotareva, Kurganov (bb0135) 2005; 70
International standard ISO 22412:2008(E) (bb0295) 2008
Borzova, Markossian, Kleymenov, Kurganov (bb0320) 2017; 7
Hall (10.1016/j.bpc.2017.10.001_bb0340) 1995; 57
Ellis (10.1016/j.bpc.2017.10.001_bb0070) 2011
Roman (10.1016/j.bpc.2017.10.001_bb0100) 2017; 100
Ellis (10.1016/j.bpc.2017.10.001_bb0015) 2001; 26
Wang (10.1016/j.bpc.2017.10.001_bb0270) 2003; 106
Singh (10.1016/j.bpc.2017.10.001_bb0170) 2005; 280
Lumry (10.1016/j.bpc.2017.10.001_bb0325) 1954; 58
Roberts (10.1016/j.bpc.2017.10.001_bb0245) 2007; 98
Chebotareva (10.1016/j.bpc.2017.10.001_bb0140) 2016; 8
Chebotareva (10.1016/j.bpc.2017.10.001_bb0050) 2013; 60
Buell (10.1016/j.bpc.2017.10.001_bb0250) 2017; 329
Borzova (10.1016/j.bpc.2017.10.001_bb0320) 2017; 7
Yang (10.1016/j.bpc.2017.10.001_bb0175) 1999; 274
Yancey (10.1016/j.bpc.2017.10.001_bb0195) 2005; 208
Kurganov (10.1016/j.bpc.2017.10.001_bb0280) 2017; 100
Chebotareva (10.1016/j.bpc.2017.10.001_bb0310) 2002; 119
Chebotareva (10.1016/j.bpc.2017.10.001_bb0040) 2007; 72
Fedurkina (10.1016/j.bpc.2017.10.001_bb0305) 2006; 71
Zhou (10.1016/j.bpc.2017.10.001_bb0125) 2008; 37
Kurganov (10.1016/j.bpc.2017.10.001_bb0265) 2002; 42
Roman (10.1016/j.bpc.2017.10.001_bb0095) 2011; 50
Eronina (10.1016/j.bpc.2017.10.001_bb0135) 2005; 70
Minton (10.1016/j.bpc.2017.10.001_bb0085) 2001; 276
Munishkina (10.1016/j.bpc.2017.10.001_bb0090) 2008; 47
Minton (10.1016/j.bpc.2017.10.001_bb0330) 1982; 79
Eronina (10.1016/j.bpc.2017.10.001_bb0285) 2016; 92
Kurganov (10.1016/j.bpc.2017.10.001_bb0260) 2002; 67
Winzor (10.1016/j.bpc.2017.10.001_bb0335) 1992; 296
Borzova (10.1016/j.bpc.2017.10.001_bb0345) 2015; 80
Chandel (10.1016/j.bpc.2017.10.001_bb0150) 2012
Despa (10.1016/j.bpc.2017.10.001_bb0205) 2004; 93
Chebotareva (10.1016/j.bpc.2017.10.001_bb0060) 2015; 76
Eronina (10.1016/j.bpc.2017.10.001_bb0230) 2009; 141
Timasheff (10.1016/j.bpc.2017.10.001_bb0190) 2002; 99
Chebotareva (10.1016/j.bpc.2017.10.001_bb0035) 2004; 69
Ellis (10.1016/j.bpc.2017.10.001_bb0065) 2006; 387
Cho (10.1016/j.bpc.2017.10.001_bb0160) 2011; 115
Hall (10.1016/j.bpc.2017.10.001_bb0025) 2003; 1649
Chebotareva (10.1016/j.bpc.2017.10.001_bb0045) 2010; 10
Kuznetsova (10.1016/j.bpc.2017.10.001_bb0080) 2014; 15
Kurganov (10.1016/j.bpc.2017.10.001_bb0300) 2002; 67
Gruebele (10.1016/j.bpc.2017.10.001_bb0075) 2016; 45
Wills (10.1016/j.bpc.2017.10.001_bb0210) 1993; 33
Eronina (10.1016/j.bpc.2017.10.001_bb0225) 2016; 86
Hill (10.1016/j.bpc.2017.10.001_bb0315) 1986
Zimmerman (10.1016/j.bpc.2017.10.001_bb0010) 1993; 22
Chebotareva (10.1016/j.bpc.2017.10.001_bb0155) 2009; 74
Hofrichter (10.1016/j.bpc.2017.10.001_bb0255) 1974; 71
Ellis (10.1016/j.bpc.2017.10.001_bb0020) 2003; 425
Canchi (10.1016/j.bpc.2017.10.001_bb0165) 2012; 116
Kurganov (10.1016/j.bpc.2017.10.001_bb0275) 2005; vol. 2
Arakawa (10.1016/j.bpc.2017.10.001_bb0185) 2006; 1764
Davis-Searles (10.1016/j.bpc.2017.10.001_bb0215) 2001; 30
Sluchanko (10.1016/j.bpc.2017.10.001_bb0105) 2015; 108
Ali (10.1016/j.bpc.2017.10.001_bb0145) 2012
Street (10.1016/j.bpc.2017.10.001_bb0200) 2006; 103
Kurganov (10.1016/j.bpc.2017.10.001_bb0120) 2013; 2
Samiotakis (10.1016/j.bpc.2017.10.001_bb0110) 2009; 10
(10.1016/j.bpc.2017.10.001_bb0290) 1995
Roberts (10.1016/j.bpc.2017.10.001_bb0240) 2006
Borwankar (10.1016/j.bpc.2017.10.001_bb0180) 2011; 50
International standard ISO 22412:2008(E) (10.1016/j.bpc.2017.10.001_bb0295) 2008
Fulton (10.1016/j.bpc.2017.10.001_bb0005) 1982; 30
Wills (10.1016/j.bpc.2017.10.001_bb0115) 2011; 158
Weatherly (10.1016/j.bpc.2017.10.001_bb0220) 2001; 10
Kastenschmidt (10.1016/j.bpc.2017.10.001_bb0235) 1968; 7
Chebotareva (10.1016/j.bpc.2017.10.001_bb0030) 2001; 268
Mukherjee (10.1016/j.bpc.2017.10.001_bb0130) 2005; 272
Chebotareva (10.1016/j.bpc.2017.10.001_bb0055) 2015; 80
References_xml – volume: 50
  start-page: 10607
  year: 2011
  end-page: 10623
  ident: bb0095
  article-title: Does the crowded cell-like environment reduce the chaperone-like activity of alpha-crystallin?
  publication-title: Biochemistry
  contributor:
    fullname: Kurganov
– volume: 387
  start-page: 485
  year: 2006
  end-page: 497
  ident: bb0065
  article-title: Protein aggregation in crowded environments
  publication-title: Biol. Chem.
  contributor:
    fullname: Minton
– year: 2008
  ident: bb0295
  article-title: Particle Size Analysis–Dynamic Light Scattering (DLS)
  contributor:
    fullname: International standard ISO 22412:2008(E)
– volume: 119
  start-page: 70
  year: 2002
  end-page: 76
  ident: bb0310
  article-title: Self-association of phosphorylase kinase from rabbit skeletal muscle in the presence of natural osmolyte, trimethylamine N-oxide
  publication-title: Progr. Colloid Polym. Sci.
  contributor:
    fullname: Harding
– volume: 80
  start-page: 130
  year: 2015
  end-page: 138
  ident: bb0345
  article-title: Kinetic regime of dithiothreitol-induced aggregation of bovine serum albumin
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 115
  start-page: 13401
  year: 2011
  end-page: 13407
  ident: bb0160
  article-title: Entropic stabilization of proteins by TMAO
  publication-title: J. Phys. Chem. B
  contributor:
    fullname: Thirumalai
– volume: 10
  start-page: 572
  year: 2009
  end-page: 588
  ident: bb0110
  article-title: Folding, stability and shape of proteins in crowded environments: experimental and computational approaches
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Cheung
– volume: 76
  start-page: 86
  year: 2015
  end-page: 93
  ident: bb0060
  article-title: Effect of Ca
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 47
  start-page: 8993
  year: 2008
  end-page: 9006
  ident: bb0090
  article-title: Guiding protein aggregation with macromolecular crowding
  publication-title: Biochemistry
  contributor:
    fullname: Uversky
– volume: 280
  start-page: 11035
  year: 2005
  end-page: 11042
  ident: bb0170
  article-title: Counteracting osmolyte trimethylamine N-oxide destabilizes proteins at pH below its pKa. Measurements of thermodynamic parameters of proteins in the presence and absence of trimethylamine N-oxide
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Ahmad
– volume: 42
  start-page: 89
  year: 2002
  end-page: 138
  ident: bb0265
  article-title: Estimation of activity of molecular chaperones in test systems based on suppression of protein aggregation
  publication-title: Uspekhi Biol. Khim.
  contributor:
    fullname: Kurganov
– volume: 296
  start-page: 102
  year: 1992
  end-page: 107
  ident: bb0335
  article-title: Rationalization of the effects of compatible solutes on protein stability in terms of thermodynamic nonideality
  publication-title: Arch. Biochem. Biophys.
  contributor:
    fullname: Naidu
– volume: 425
  start-page: 27
  year: 2003
  end-page: 28
  ident: bb0020
  article-title: Cell biology: join the crowd
  publication-title: Nature
  contributor:
    fullname: Minton
– volume: 8
  start-page: 397
  year: 2016
  end-page: 407
  ident: bb0140
  article-title: Dissociative mechanism for irreversible thermal denaturation of oligomeric proteins
  publication-title: Biophys. Rev.
  contributor:
    fullname: Kurganov
– volume: 86
  start-page: 829
  year: 2016
  end-page: 839
  ident: bb0225
  article-title: Checking for reversibility of aggregation of UV-irradiated glycogen phosphorylase b under crowding conditions
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 67
  start-page: 525
  year: 2002
  end-page: 533
  ident: bb0300
  article-title: Kinetics of thermal aggregation of tobacco mosaic virus coat protein
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Dobrov
– volume: 268
  start-page: 506
  year: 2001
  end-page: 513
  ident: bb0030
  article-title: Ultracentrifugal studies of the effect of molecular crowding by trimethylamine N-oxide on the self-association of muscle glycogen phosphorylase
  publication-title: Eur. J. Biochem.
  contributor:
    fullname: Winzor
– volume: 93
  start-page: 228104
  year: 2004
  ident: bb0205
  article-title: Dielectric modulation of biological water
  publication-title: Phys. Rev. Lett.
  contributor:
    fullname: Berry
– volume: 80
  start-page: 358
  year: 2015
  end-page: 365
  ident: bb0055
  article-title: Effect of crowding on several stages of protein aggregation in test systems in the presence of alpha-crystallin
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 272
  start-page: 2760
  year: 2005
  end-page: 2772
  ident: bb0130
  article-title: A natural osmolyte trimethylamine N-oxide promotes assembly and bundling of the bacterial cell division protein, FtsZ and counteracts the denaturing effects of urea
  publication-title: FEBS J.
  contributor:
    fullname: Panda
– volume: 2
  year: 2013
  ident: bb0120
  article-title: The functioning of chaperones possessing the anti-aggregation activity in a crowded medium
  publication-title: Biochem. Anal. Biochem.
  contributor:
    fullname: Chebotareva
– volume: 74
  start-page: 562
  year: 2009
  end-page: 568
  ident: bb0155
  article-title: Glycogen phosphorylase
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Kurganov
– volume: 71
  start-page: 4864
  year: 1974
  end-page: 4868
  ident: bb0255
  article-title: Kinetics and mechanism of deoxyhemoglobin S gelation: a new approach to understanding sickle cell disease
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  contributor:
    fullname: Eaton
– volume: 7
  start-page: 3590
  year: 1968
  end-page: 3608
  ident: bb0235
  article-title: Subunit interactions and their relationship to the allosteric properties of rabbit skeletal muscle phosphorylase
  publication-title: Biochemistry
  contributor:
    fullname: Helmreich
– volume: 108
  start-page: 68
  year: 2015
  end-page: 75
  ident: bb0105
  article-title: Quaternary structure of human small heat shock protein HSPB6 (Hsp20) in crowded media modeled by trimethylamine N-oxide (TMAO): effect of protein phosphorylation
  publication-title: Biochimie
  contributor:
    fullname: Gusev
– start-page: 35
  year: 2012
  end-page: 53
  ident: bb0145
  article-title: Protein-osmolyte interactions: molecular insights
  publication-title: Cellular Osmolytes
  contributor:
    fullname: Ansari
– volume: 22
  start-page: 27
  year: 1993
  end-page: 65
  ident: bb0010
  article-title: Macromolecular crowding: biochemical, biophysical, and physiological consequences
  publication-title: Annu. Rev. Biophys. Biomol. Struct.
  contributor:
    fullname: Minton
– volume: 70
  start-page: 1020
  year: 2005
  end-page: 1026
  ident: bb0135
  article-title: Influence of osmolytes on inactivation and aggregation of muscle glycogen phosphorylase
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Kurganov
– volume: 10
  start-page: 12
  year: 2001
  end-page: 16
  ident: bb0220
  article-title: Second virial coefficients as a measure of protein-osmolyte interactions
  publication-title: Protein Sci.
  contributor:
    fullname: Pielak
– volume: 100
  start-page: 104
  year: 2017
  end-page: 119
  ident: bb0280
  article-title: Quantification of anti-aggregation activity of chaperones
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 1764
  start-page: 1677
  year: 2006
  end-page: 1687
  ident: bb0185
  article-title: Small molecule pharmacological chaperones: from thermodynamic stabilization to pharmaceutical drugs
  publication-title: Biochim. Biophys. Acta
  contributor:
    fullname: Tsumoto
– volume: 30
  start-page: 271
  year: 2001
  end-page: 306
  ident: bb0215
  article-title: Interpreting the effects of small uncharged solutes on protein-folding equilibria
  publication-title: Annu. Rev. Biophys. Biomol. Struct.
  contributor:
    fullname: Pielak
– volume: 99
  start-page: 9721
  year: 2002
  end-page: 9726
  ident: bb0190
  article-title: Protein-solvent preferential interactions, protein hydration, and the modulation of biochemical reactions by solvent components
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  contributor:
    fullname: Timasheff
– volume: 106
  start-page: 97
  year: 2003
  end-page: 109
  ident: bb0270
  article-title: Kinetics of heat- and acidification-induced aggregation of firefly luciferase
  publication-title: Biophys. Chem.
  contributor:
    fullname: Kurganov
– volume: 69
  start-page: 1239
  year: 2004
  end-page: 1251
  ident: bb0035
  article-title: Biochemical effects of molecular crowding
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Livanova
– start-page: 143
  year: 2012
  end-page: 160
  ident: bb0150
  article-title: Impact of osmolytes in conformational modulation of protein and its application in biotechnology
  publication-title: Cellular Osmolytes
  contributor:
    fullname: Khan
– volume: 116
  start-page: 12095
  year: 2012
  end-page: 12104
  ident: bb0165
  article-title: Molecular mechanism for the preferential exclusion of TMAO from protein surfaces
  publication-title: J. Phys. Chem. B
  contributor:
    fullname: Garcia
– volume: 103
  start-page: 13997
  year: 2006
  end-page: 14002
  ident: bb0200
  article-title: A molecular mechanism for osmolyte-induced protein stability
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  contributor:
    fullname: Rose
– volume: 100
  start-page: 97
  year: 2017
  end-page: 103
  ident: bb0100
  article-title: Anti-aggregation activity of small heat shock proteins under crowded conditions
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 1649
  start-page: 127
  year: 2003
  end-page: 139
  ident: bb0025
  article-title: Macromolecular crowding: qualitative and semiquantitative successes, quantitative challenges
  publication-title: Biochim. Biophys. Acta
  contributor:
    fullname: Minton
– volume: 30
  start-page: 345
  year: 1982
  end-page: 347
  ident: bb0005
  article-title: How crowded is the cytoplasm?
  publication-title: Cell
  contributor:
    fullname: Fulton
– volume: 45
  start-page: 233
  year: 2016
  end-page: 251
  ident: bb0075
  article-title: Globular protein folding in vitro and in vivo
  publication-title: Annu. Rev. Biophys.
  contributor:
    fullname: Sukenik
– volume: 10
  start-page: 783
  year: 2010
  end-page: 789
  ident: bb0045
  article-title: Interaction of Hsp27 with native phosphorylase kinase under crowding conditions
  publication-title: Macromol. Biosci.
  contributor:
    fullname: Kurganov
– volume: 37
  start-page: 375
  year: 2008
  end-page: 397
  ident: bb0125
  article-title: Macromolecular crowding and confinement: biochemical, biophysical, and potential physiological consequences
  publication-title: Annu. Rev. Biophys.
  contributor:
    fullname: Minton
– volume: 92
  start-page: 1252
  year: 2016
  end-page: 1257
  ident: bb0285
  article-title: Kinetic regime of thermal aggregation of holo- and apoglycogen phosphorylase
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 7
  start-page: 3984
  year: 2017
  ident: bb0320
  article-title: A change in the pathway of dithiothreitol-induced aggregation of bovine serum albumin in the presence of polyamines and arginine
  publication-title: Sci Rep
  contributor:
    fullname: Kurganov
– year: 1986
  ident: bb0315
  article-title: An Introduction to Statistical Thermodynamics
  contributor:
    fullname: Hill
– volume: 329
  start-page: 187
  year: 2017
  end-page: 226
  ident: bb0250
  article-title: The nucleation of protein aggregates - from crystals to amyloid fibrils
  publication-title: Int. Rev. Cell Mol. Biol.
  contributor:
    fullname: Buell
– start-page: 466
  year: 1995
  ident: bb0290
  publication-title: Scientist for Experimental Data Fitting. Microsoft Windows Version 2.0
– volume: 60
  start-page: 69
  year: 2013
  end-page: 76
  ident: bb0050
  article-title: Effect of crowding and chaperones on self-association, aggregation and reconstitution of apophosphorylase
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Kurganov
– volume: 57
  start-page: 47
  year: 1995
  end-page: 54
  ident: bb0340
  article-title: Stabilizing effect of sucrose against irreversible denaturation of rabbit muscle lactate dehydrogenase
  publication-title: Biophys. Chem.
  contributor:
    fullname: Winzor
– volume: vol. 2
  start-page: 251
  year: 2005
  end-page: 279
  ident: bb0275
  article-title: Protein aggregation kinetics
  publication-title: Chemical and Biological Kinetics. New Horizons
  contributor:
    fullname: Kurganov
– volume: 158
  start-page: 21
  year: 2011
  end-page: 25
  ident: bb0115
  article-title: Allowance for thermodynamic nonideality in the characterization of protein interactions by spectral techniques
  publication-title: Biophys. Chem.
  contributor:
    fullname: Winzor
– volume: 58
  start-page: 110
  year: 1954
  end-page: 120
  ident: bb0325
  article-title: Conformation changes of protein
  publication-title: J. Phys. Chem.
  contributor:
    fullname: Erying
– volume: 67
  start-page: 409
  year: 2002
  end-page: 422
  ident: bb0260
  article-title: Kinetics of protein aggregation. Quantitative estimation of the chaperone-like activity in test-systems based on suppression of protein aggregation
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Kurganov
– volume: 50
  start-page: 2048
  year: 2011
  end-page: 2060
  ident: bb0180
  article-title: Natural osmolytes remodel the aggregation pathway of mutant
  publication-title: Biochemistry
  contributor:
    fullname: Ignatova
– volume: 26
  start-page: 597
  year: 2001
  end-page: 604
  ident: bb0015
  article-title: Macromolecular crowding: obvious but underappreciated
  publication-title: Trends Biochem. Sci.
  contributor:
    fullname: Ellis
– volume: 208
  start-page: 2819
  year: 2005
  end-page: 2830
  ident: bb0195
  article-title: Organic osmolytes as compatible, metabolic and counteracting cytoprotectants in high osmolarity and other stresses
  publication-title: J. Exp. Biol.
  contributor:
    fullname: Yancey
– volume: 79
  start-page: 7107
  year: 1982
  end-page: 7111
  ident: bb0330
  article-title: Nonspecific stabilization of stress-susceptible proteins by stress-resistant proteins: a model for the biological role of heat shock proteins
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  contributor:
    fullname: Minton
– volume: 71
  start-page: 325
  year: 2006
  end-page: 331
  ident: bb0305
  article-title: Change in kinetic regime of protein aggregation with temperature increase. Thermal aggregation of rabbit muscle creatine kinase
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Kurganov
– volume: 72
  start-page: 1478
  year: 2007
  end-page: 1490
  ident: bb0040
  article-title: Effect of molecular crowding on the enzymes of glycogenolysis
  publication-title: Biochemistry (Mosc)
  contributor:
    fullname: Chebotareva
– start-page: 17
  year: 2006
  end-page: 46
  ident: bb0240
  article-title: Nonnative protein aggregation. Pathways, kinetics, and stability prediction
  publication-title: Misbehaving Proteins. Protein (Mis)Folding, Aggregation, and Stability
  contributor:
    fullname: Roberts
– volume: 15
  start-page: 23090
  year: 2014
  end-page: 23140
  ident: bb0080
  article-title: What macromolecular crowding can do to a protein
  publication-title: Int. J. Mol. Sci.
  contributor:
    fullname: Uversky
– volume: 141
  start-page: 66
  year: 2009
  end-page: 74
  ident: bb0230
  article-title: Effect of proline on thermal inactivation, denaturation and aggregation of glycogen phosphorylase b from rabbit skeletal muscle
  publication-title: Biophys. Chem.
  contributor:
    fullname: Kurganov
– start-page: 9
  year: 2011
  end-page: 34
  ident: bb0070
  article-title: Protein aggregation: opposing effects of chaperones and crowding
  publication-title: Folding for the Synapse
  contributor:
    fullname: Ellis
– volume: 98
  start-page: 927
  year: 2007
  end-page: 938
  ident: bb0245
  article-title: Non-native protein aggregation kinetics
  publication-title: Biotechnol. Bioeng.
  contributor:
    fullname: Roberts
– volume: 274
  start-page: 32970
  year: 1999
  end-page: 32974
  ident: bb0175
  article-title: Manipulating the amyloid-beta aggregation pathway with chemical chaperones
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Fraser
– volume: 276
  start-page: 10577
  year: 2001
  end-page: 10580
  ident: bb0085
  article-title: The influence of macromolecular crowding and macromolecular confinement on biochemical reactions in physiological media
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Minton
– volume: 33
  start-page: 1627
  year: 1993
  end-page: 1629
  ident: bb0210
  article-title: Thermodynamic analysis of “preferential solvation” in protein solutions
  publication-title: Biopolymers
  contributor:
    fullname: Winzor
– volume: 30
  start-page: 345
  year: 1982
  ident: 10.1016/j.bpc.2017.10.001_bb0005
  article-title: How crowded is the cytoplasm?
  publication-title: Cell
  doi: 10.1016/0092-8674(82)90231-8
  contributor:
    fullname: Fulton
– volume: 425
  start-page: 27
  year: 2003
  ident: 10.1016/j.bpc.2017.10.001_bb0020
  article-title: Cell biology: join the crowd
  publication-title: Nature
  doi: 10.1038/425027a
  contributor:
    fullname: Ellis
– volume: 106
  start-page: 97
  year: 2003
  ident: 10.1016/j.bpc.2017.10.001_bb0270
  article-title: Kinetics of heat- and acidification-induced aggregation of firefly luciferase
  publication-title: Biophys. Chem.
  doi: 10.1016/S0301-4622(03)00134-0
  contributor:
    fullname: Wang
– volume: 1649
  start-page: 127
  year: 2003
  ident: 10.1016/j.bpc.2017.10.001_bb0025
  article-title: Macromolecular crowding: qualitative and semiquantitative successes, quantitative challenges
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/S1570-9639(03)00167-5
  contributor:
    fullname: Hall
– volume: 10
  start-page: 12
  year: 2001
  ident: 10.1016/j.bpc.2017.10.001_bb0220
  article-title: Second virial coefficients as a measure of protein-osmolyte interactions
  publication-title: Protein Sci.
  doi: 10.1110/ps.29301
  contributor:
    fullname: Weatherly
– volume: 58
  start-page: 110
  year: 1954
  ident: 10.1016/j.bpc.2017.10.001_bb0325
  article-title: Conformation changes of protein
  publication-title: J. Phys. Chem.
  doi: 10.1021/j150512a005
  contributor:
    fullname: Lumry
– volume: 70
  start-page: 1020
  year: 2005
  ident: 10.1016/j.bpc.2017.10.001_bb0135
  article-title: Influence of osmolytes on inactivation and aggregation of muscle glycogen phosphorylase b by guanidine hydrochloride. Stimulation of protein aggregation under crowding conditions
  publication-title: Biochemistry (Mosc)
  doi: 10.1007/s10541-005-0219-8
  contributor:
    fullname: Eronina
– volume: 268
  start-page: 506
  year: 2001
  ident: 10.1016/j.bpc.2017.10.001_bb0030
  article-title: Ultracentrifugal studies of the effect of molecular crowding by trimethylamine N-oxide on the self-association of muscle glycogen phosphorylase b
  publication-title: Eur. J. Biochem.
  doi: 10.1046/j.1432-1327.2001.01838.x
  contributor:
    fullname: Chebotareva
– volume: 329
  start-page: 187
  year: 2017
  ident: 10.1016/j.bpc.2017.10.001_bb0250
  article-title: The nucleation of protein aggregates - from crystals to amyloid fibrils
  publication-title: Int. Rev. Cell Mol. Biol.
  doi: 10.1016/bs.ircmb.2016.08.014
  contributor:
    fullname: Buell
– volume: 387
  start-page: 485
  year: 2006
  ident: 10.1016/j.bpc.2017.10.001_bb0065
  article-title: Protein aggregation in crowded environments
  publication-title: Biol. Chem.
  doi: 10.1515/BC.2006.064
  contributor:
    fullname: Ellis
– volume: 10
  start-page: 572
  year: 2009
  ident: 10.1016/j.bpc.2017.10.001_bb0110
  article-title: Folding, stability and shape of proteins in crowded environments: experimental and computational approaches
  publication-title: Int. J. Biol. Macromol.
  contributor:
    fullname: Samiotakis
– volume: 57
  start-page: 47
  year: 1995
  ident: 10.1016/j.bpc.2017.10.001_bb0340
  article-title: Stabilizing effect of sucrose against irreversible denaturation of rabbit muscle lactate dehydrogenase
  publication-title: Biophys. Chem.
  doi: 10.1016/0301-4622(95)00044-X
  contributor:
    fullname: Hall
– volume: 60
  start-page: 69
  year: 2013
  ident: 10.1016/j.bpc.2017.10.001_bb0050
  article-title: Effect of crowding and chaperones on self-association, aggregation and reconstitution of apophosphorylase b
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2013.05.010
  contributor:
    fullname: Chebotareva
– volume: 71
  start-page: 325
  year: 2006
  ident: 10.1016/j.bpc.2017.10.001_bb0305
  article-title: Change in kinetic regime of protein aggregation with temperature increase. Thermal aggregation of rabbit muscle creatine kinase
  publication-title: Biochemistry (Mosc)
  doi: 10.1134/S000629790603014X
  contributor:
    fullname: Fedurkina
– volume: 276
  start-page: 10577
  year: 2001
  ident: 10.1016/j.bpc.2017.10.001_bb0085
  article-title: The influence of macromolecular crowding and macromolecular confinement on biochemical reactions in physiological media
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.R100005200
  contributor:
    fullname: Minton
– volume: 93
  start-page: 228104
  year: 2004
  ident: 10.1016/j.bpc.2017.10.001_bb0205
  article-title: Dielectric modulation of biological water
  publication-title: Phys. Rev. Lett.
  doi: 10.1103/PhysRevLett.93.228104
  contributor:
    fullname: Despa
– volume: 272
  start-page: 2760
  year: 2005
  ident: 10.1016/j.bpc.2017.10.001_bb0130
  article-title: A natural osmolyte trimethylamine N-oxide promotes assembly and bundling of the bacterial cell division protein, FtsZ and counteracts the denaturing effects of urea
  publication-title: FEBS J.
  doi: 10.1111/j.1742-4658.2005.04696.x
  contributor:
    fullname: Mukherjee
– volume: 119
  start-page: 70
  year: 2002
  ident: 10.1016/j.bpc.2017.10.001_bb0310
  article-title: Self-association of phosphorylase kinase from rabbit skeletal muscle in the presence of natural osmolyte, trimethylamine N-oxide
  publication-title: Progr. Colloid Polym. Sci.
  doi: 10.1007/3-540-44672-9_11
  contributor:
    fullname: Chebotareva
– volume: 86
  start-page: 829
  year: 2016
  ident: 10.1016/j.bpc.2017.10.001_bb0225
  article-title: Checking for reversibility of aggregation of UV-irradiated glycogen phosphorylase b under crowding conditions
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2016.02.010
  contributor:
    fullname: Eronina
– volume: 42
  start-page: 89
  year: 2002
  ident: 10.1016/j.bpc.2017.10.001_bb0265
  article-title: Estimation of activity of molecular chaperones in test systems based on suppression of protein aggregation
  publication-title: Uspekhi Biol. Khim.
  contributor:
    fullname: Kurganov
– volume: 116
  start-page: 12095
  year: 2012
  ident: 10.1016/j.bpc.2017.10.001_bb0165
  article-title: Molecular mechanism for the preferential exclusion of TMAO from protein surfaces
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp304298c
  contributor:
    fullname: Canchi
– volume: 1764
  start-page: 1677
  year: 2006
  ident: 10.1016/j.bpc.2017.10.001_bb0185
  article-title: Small molecule pharmacological chaperones: from thermodynamic stabilization to pharmaceutical drugs
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/j.bbapap.2006.08.012
  contributor:
    fullname: Arakawa
– volume: 141
  start-page: 66
  year: 2009
  ident: 10.1016/j.bpc.2017.10.001_bb0230
  article-title: Effect of proline on thermal inactivation, denaturation and aggregation of glycogen phosphorylase b from rabbit skeletal muscle
  publication-title: Biophys. Chem.
  doi: 10.1016/j.bpc.2008.12.007
  contributor:
    fullname: Eronina
– volume: 67
  start-page: 525
  year: 2002
  ident: 10.1016/j.bpc.2017.10.001_bb0300
  article-title: Kinetics of thermal aggregation of tobacco mosaic virus coat protein
  publication-title: Biochemistry (Mosc)
  doi: 10.1023/A:1015589926728
  contributor:
    fullname: Kurganov
– year: 1986
  ident: 10.1016/j.bpc.2017.10.001_bb0315
  contributor:
    fullname: Hill
– volume: 296
  start-page: 102
  year: 1992
  ident: 10.1016/j.bpc.2017.10.001_bb0335
  article-title: Rationalization of the effects of compatible solutes on protein stability in terms of thermodynamic nonideality
  publication-title: Arch. Biochem. Biophys.
  doi: 10.1016/0003-9861(92)90550-G
  contributor:
    fullname: Winzor
– volume: 80
  start-page: 358
  year: 2015
  ident: 10.1016/j.bpc.2017.10.001_bb0055
  article-title: Effect of crowding on several stages of protein aggregation in test systems in the presence of alpha-crystallin
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2015.07.002
  contributor:
    fullname: Chebotareva
– start-page: 35
  year: 2012
  ident: 10.1016/j.bpc.2017.10.001_bb0145
  article-title: Protein-osmolyte interactions: molecular insights
  contributor:
    fullname: Ali
– volume: 67
  start-page: 409
  year: 2002
  ident: 10.1016/j.bpc.2017.10.001_bb0260
  article-title: Kinetics of protein aggregation. Quantitative estimation of the chaperone-like activity in test-systems based on suppression of protein aggregation
  publication-title: Biochemistry (Mosc)
  doi: 10.1023/A:1015277805345
  contributor:
    fullname: Kurganov
– volume: 74
  start-page: 562
  year: 2009
  ident: 10.1016/j.bpc.2017.10.001_bb0155
  article-title: Glycogen phosphorylase b and phosphorylase kinase binding to glycogen under molecular crowding conditions. Inhibitory effect of FAD
  publication-title: Biochemistry (Mosc)
  doi: 10.1134/S0006297909050125
  contributor:
    fullname: Chebotareva
– volume: 69
  start-page: 1239
  year: 2004
  ident: 10.1016/j.bpc.2017.10.001_bb0035
  article-title: Biochemical effects of molecular crowding
  publication-title: Biochemistry (Mosc)
  doi: 10.1007/s10541-005-0070-y
  contributor:
    fullname: Chebotareva
– volume: 7
  start-page: 3590
  year: 1968
  ident: 10.1016/j.bpc.2017.10.001_bb0235
  article-title: Subunit interactions and their relationship to the allosteric properties of rabbit skeletal muscle phosphorylase b
  publication-title: Biochemistry
  doi: 10.1021/bi00850a037
  contributor:
    fullname: Kastenschmidt
– volume: 103
  start-page: 13997
  year: 2006
  ident: 10.1016/j.bpc.2017.10.001_bb0200
  article-title: A molecular mechanism for osmolyte-induced protein stability
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.0606236103
  contributor:
    fullname: Street
– volume: 158
  start-page: 21
  year: 2011
  ident: 10.1016/j.bpc.2017.10.001_bb0115
  article-title: Allowance for thermodynamic nonideality in the characterization of protein interactions by spectral techniques
  publication-title: Biophys. Chem.
  doi: 10.1016/j.bpc.2011.04.011
  contributor:
    fullname: Wills
– volume: 80
  start-page: 130
  year: 2015
  ident: 10.1016/j.bpc.2017.10.001_bb0345
  article-title: Kinetic regime of dithiothreitol-induced aggregation of bovine serum albumin
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2015.06.040
  contributor:
    fullname: Borzova
– start-page: 143
  year: 2012
  ident: 10.1016/j.bpc.2017.10.001_bb0150
  article-title: Impact of osmolytes in conformational modulation of protein and its application in biotechnology
  contributor:
    fullname: Chandel
– volume: 50
  start-page: 10607
  year: 2011
  ident: 10.1016/j.bpc.2017.10.001_bb0095
  article-title: Does the crowded cell-like environment reduce the chaperone-like activity of alpha-crystallin?
  publication-title: Biochemistry
  doi: 10.1021/bi201030y
  contributor:
    fullname: Roman
– volume: 100
  start-page: 97
  year: 2017
  ident: 10.1016/j.bpc.2017.10.001_bb0100
  article-title: Anti-aggregation activity of small heat shock proteins under crowded conditions
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2016.05.080
  contributor:
    fullname: Roman
– volume: 2
  year: 2013
  ident: 10.1016/j.bpc.2017.10.001_bb0120
  article-title: The functioning of chaperones possessing the anti-aggregation activity in a crowded medium
  publication-title: Biochem. Anal. Biochem.
  doi: 10.4172/2161-1009.1000e138
  contributor:
    fullname: Kurganov
– volume: 22
  start-page: 27
  year: 1993
  ident: 10.1016/j.bpc.2017.10.001_bb0010
  article-title: Macromolecular crowding: biochemical, biophysical, and physiological consequences
  publication-title: Annu. Rev. Biophys. Biomol. Struct.
  doi: 10.1146/annurev.bb.22.060193.000331
  contributor:
    fullname: Zimmerman
– volume: 280
  start-page: 11035
  year: 2005
  ident: 10.1016/j.bpc.2017.10.001_bb0170
  article-title: Counteracting osmolyte trimethylamine N-oxide destabilizes proteins at pH below its pKa. Measurements of thermodynamic parameters of proteins in the presence and absence of trimethylamine N-oxide
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M410716200
  contributor:
    fullname: Singh
– volume: 108
  start-page: 68
  year: 2015
  ident: 10.1016/j.bpc.2017.10.001_bb0105
  article-title: Quaternary structure of human small heat shock protein HSPB6 (Hsp20) in crowded media modeled by trimethylamine N-oxide (TMAO): effect of protein phosphorylation
  publication-title: Biochimie
  doi: 10.1016/j.biochi.2014.11.001
  contributor:
    fullname: Sluchanko
– volume: 45
  start-page: 233
  year: 2016
  ident: 10.1016/j.bpc.2017.10.001_bb0075
  article-title: Globular protein folding in vitro and in vivo
  publication-title: Annu. Rev. Biophys.
  doi: 10.1146/annurev-biophys-062215-011236
  contributor:
    fullname: Gruebele
– volume: 33
  start-page: 1627
  year: 1993
  ident: 10.1016/j.bpc.2017.10.001_bb0210
  article-title: Thermodynamic analysis of “preferential solvation” in protein solutions
  publication-title: Biopolymers
  doi: 10.1002/bip.360331012
  contributor:
    fullname: Wills
– start-page: 9
  year: 2011
  ident: 10.1016/j.bpc.2017.10.001_bb0070
  article-title: Protein aggregation: opposing effects of chaperones and crowding
  contributor:
    fullname: Ellis
– volume: 26
  start-page: 597
  year: 2001
  ident: 10.1016/j.bpc.2017.10.001_bb0015
  article-title: Macromolecular crowding: obvious but underappreciated
  publication-title: Trends Biochem. Sci.
  doi: 10.1016/S0968-0004(01)01938-7
  contributor:
    fullname: Ellis
– volume: 15
  start-page: 23090
  year: 2014
  ident: 10.1016/j.bpc.2017.10.001_bb0080
  article-title: What macromolecular crowding can do to a protein
  publication-title: Int. J. Mol. Sci.
  doi: 10.3390/ijms151223090
  contributor:
    fullname: Kuznetsova
– volume: 8
  start-page: 397
  year: 2016
  ident: 10.1016/j.bpc.2017.10.001_bb0140
  article-title: Dissociative mechanism for irreversible thermal denaturation of oligomeric proteins
  publication-title: Biophys. Rev.
  doi: 10.1007/s12551-016-0220-z
  contributor:
    fullname: Chebotareva
– volume: 274
  start-page: 32970
  year: 1999
  ident: 10.1016/j.bpc.2017.10.001_bb0175
  article-title: Manipulating the amyloid-beta aggregation pathway with chemical chaperones
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.274.46.32970
  contributor:
    fullname: Yang
– volume: 50
  start-page: 2048
  year: 2011
  ident: 10.1016/j.bpc.2017.10.001_bb0180
  article-title: Natural osmolytes remodel the aggregation pathway of mutant
  publication-title: Biochemistry
  doi: 10.1021/bi1018368
  contributor:
    fullname: Borwankar
– volume: 71
  start-page: 4864
  year: 1974
  ident: 10.1016/j.bpc.2017.10.001_bb0255
  article-title: Kinetics and mechanism of deoxyhemoglobin S gelation: a new approach to understanding sickle cell disease
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.71.12.4864
  contributor:
    fullname: Hofrichter
– volume: 72
  start-page: 1478
  year: 2007
  ident: 10.1016/j.bpc.2017.10.001_bb0040
  article-title: Effect of molecular crowding on the enzymes of glycogenolysis
  publication-title: Biochemistry (Mosc)
  doi: 10.1134/S0006297907130056
  contributor:
    fullname: Chebotareva
– volume: 100
  start-page: 104
  year: 2017
  ident: 10.1016/j.bpc.2017.10.001_bb0280
  article-title: Quantification of anti-aggregation activity of chaperones
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2016.07.066
  contributor:
    fullname: Kurganov
– volume: 92
  start-page: 1252
  year: 2016
  ident: 10.1016/j.bpc.2017.10.001_bb0285
  article-title: Kinetic regime of thermal aggregation of holo- and apoglycogen phosphorylase b
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2016.08.038
  contributor:
    fullname: Eronina
– volume: 99
  start-page: 9721
  year: 2002
  ident: 10.1016/j.bpc.2017.10.001_bb0190
  article-title: Protein-solvent preferential interactions, protein hydration, and the modulation of biochemical reactions by solvent components
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.122225399
  contributor:
    fullname: Timasheff
– year: 2008
  ident: 10.1016/j.bpc.2017.10.001_bb0295
  contributor:
    fullname: International standard ISO 22412:2008(E)
– volume: 10
  start-page: 783
  year: 2010
  ident: 10.1016/j.bpc.2017.10.001_bb0045
  article-title: Interaction of Hsp27 with native phosphorylase kinase under crowding conditions
  publication-title: Macromol. Biosci.
  doi: 10.1002/mabi.200900397
  contributor:
    fullname: Chebotareva
– start-page: 17
  year: 2006
  ident: 10.1016/j.bpc.2017.10.001_bb0240
  article-title: Nonnative protein aggregation. Pathways, kinetics, and stability prediction
  contributor:
    fullname: Roberts
– volume: 208
  start-page: 2819
  year: 2005
  ident: 10.1016/j.bpc.2017.10.001_bb0195
  article-title: Organic osmolytes as compatible, metabolic and counteracting cytoprotectants in high osmolarity and other stresses
  publication-title: J. Exp. Biol.
  doi: 10.1242/jeb.01730
  contributor:
    fullname: Yancey
– volume: 37
  start-page: 375
  year: 2008
  ident: 10.1016/j.bpc.2017.10.001_bb0125
  article-title: Macromolecular crowding and confinement: biochemical, biophysical, and potential physiological consequences
  publication-title: Annu. Rev. Biophys.
  doi: 10.1146/annurev.biophys.37.032807.125817
  contributor:
    fullname: Zhou
– volume: vol. 2
  start-page: 251
  year: 2005
  ident: 10.1016/j.bpc.2017.10.001_bb0275
  article-title: Protein aggregation kinetics
  contributor:
    fullname: Kurganov
– start-page: 466
  year: 1995
  ident: 10.1016/j.bpc.2017.10.001_bb0290
– volume: 79
  start-page: 7107
  year: 1982
  ident: 10.1016/j.bpc.2017.10.001_bb0330
  article-title: Nonspecific stabilization of stress-susceptible proteins by stress-resistant proteins: a model for the biological role of heat shock proteins
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.79.23.7107
  contributor:
    fullname: Minton
– volume: 47
  start-page: 8993
  year: 2008
  ident: 10.1016/j.bpc.2017.10.001_bb0090
  article-title: Guiding protein aggregation with macromolecular crowding
  publication-title: Biochemistry
  doi: 10.1021/bi8008399
  contributor:
    fullname: Munishkina
– volume: 98
  start-page: 927
  year: 2007
  ident: 10.1016/j.bpc.2017.10.001_bb0245
  article-title: Non-native protein aggregation kinetics
  publication-title: Biotechnol. Bioeng.
  doi: 10.1002/bit.21627
  contributor:
    fullname: Roberts
– volume: 76
  start-page: 86
  year: 2015
  ident: 10.1016/j.bpc.2017.10.001_bb0060
  article-title: Effect of Ca2+ and Mg2+ ions on oligomeric state and chaperone-like activity of αB-crystallin in crowded media
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2015.02.022
  contributor:
    fullname: Chebotareva
– volume: 115
  start-page: 13401
  year: 2011
  ident: 10.1016/j.bpc.2017.10.001_bb0160
  article-title: Entropic stabilization of proteins by TMAO
  publication-title: J. Phys. Chem. B
  doi: 10.1021/jp207289b
  contributor:
    fullname: Cho
– volume: 30
  start-page: 271
  year: 2001
  ident: 10.1016/j.bpc.2017.10.001_bb0215
  article-title: Interpreting the effects of small uncharged solutes on protein-folding equilibria
  publication-title: Annu. Rev. Biophys. Biomol. Struct.
  doi: 10.1146/annurev.biophys.30.1.271
  contributor:
    fullname: Davis-Searles
– volume: 7
  start-page: 3984
  year: 2017
  ident: 10.1016/j.bpc.2017.10.001_bb0320
  article-title: A change in the pathway of dithiothreitol-induced aggregation of bovine serum albumin in the presence of polyamines and arginine
  publication-title: Sci Rep
  doi: 10.1038/s41598-017-04409-x
  contributor:
    fullname: Borzova
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Snippet To characterize the initial stages of protein aggregation, the kinetics of aggregation of UV-irradiated glycogen phosphorylase b (UV-Phb) was studied under...
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SubjectTerms Animals
Crowding
Dynamic Light Scattering
Enzyme Inhibitors - chemistry
Enzyme Inhibitors - pharmacology
Ficoll - chemistry
Ficoll - pharmacology
Glycogen phosphorylase b
Glycogen Phosphorylase, Muscle Form - antagonists & inhibitors
Glycogen Phosphorylase, Muscle Form - isolation & purification
Glycogen Phosphorylase, Muscle Form - metabolism
Kinetic regime
Kinetics
Methylamines - chemistry
Methylamines - pharmacology
Polyethylene Glycols - chemistry
Polyethylene Glycols - pharmacology
Protein Aggregates - drug effects
Protein aggregation
Rabbits
Temperature
Ultraviolet Rays
Title Mechanism of aggregation of UV-irradiated glycogen phosphorylase b at a low temperature in the presence of crowders and trimethylamine N-oxide
URI https://dx.doi.org/10.1016/j.bpc.2017.10.001
https://www.ncbi.nlm.nih.gov/pubmed/29054581
https://search.proquest.com/docview/1954075600
Volume 232
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