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 |
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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.
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•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. |
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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. |
Author_xml | – sequence: 1 givenname: Tatiana B. surname: Eronina fullname: Eronina, Tatiana B. email: eronina@inbi.ras.ru organization: Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, 33, bld. 2, Leninsky Ave., Moscow 119071, Russia – sequence: 2 givenname: Valeriya V. surname: Mikhaylova fullname: Mikhaylova, Valeriya V. organization: Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, 33, bld. 2, Leninsky Ave., Moscow 119071, Russia – sequence: 3 givenname: Natalia A. surname: Chebotareva fullname: Chebotareva, Natalia A. organization: Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, 33, bld. 2, Leninsky Ave., Moscow 119071, Russia – sequence: 4 givenname: Vera A. surname: Borzova fullname: Borzova, Vera A. organization: Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, 33, bld. 2, Leninsky Ave., Moscow 119071, Russia – sequence: 5 givenname: Igor K. surname: Yudin fullname: Yudin, Igor K. organization: Oil and Gas Research Institute, Russian Academy of Sciences, Gubkina st. 3, 117971 Moscow, Russia – sequence: 6 givenname: Boris I. surname: Kurganov fullname: Kurganov, Boris I. 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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Keywords | Kinetic regime Protein aggregation Glycogen phosphorylase b Crowding |
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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 |
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