Search Results - "Roth, Christopher B."

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    Structural Basis for Allosteric Regulation of GPCRs by Sodium Ions by Liu, Wei, Chun, Eugene, Thompson, Aaron A., Chubukov, Pavel, Xu, Fei, Katritch, Vsevolod, Han, Gye Won, Roth, Christopher B., Heitman, Laura H., IJzerman, Adriaan P., Cherezov, Vadim, Stevens, Raymond C.

    “…Pharmacological responses of G protein-coupled receptors (GPCRs) can be fine-tuned by allosteric modulators. Structural studies of such effects have been…”
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    Journal Article
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    Fusion Partner Toolchest for the Stabilization and Crystallization of G Protein-Coupled Receptors by Chun, Eugene, Thompson, Aaron A., Liu, Wei, Roth, Christopher B., Griffith, Mark T., Katritch, Vsevolod, Kunken, Joshua, Xu, Fei, Cherezov, Vadim, Hanson, Michael A., Stevens, Raymond C.

    Published in Structure (London) (06-06-2012)
    “…Structural studies of human G protein-coupled receptors (GPCRs) have recently been accelerated through the use of a fusion partner that was inserted into the…”
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    Journal Article
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    Flexibility in the ABC Transporter MsbA: Alternating Access with a Twist by Ward, Andrew, Reyes, Christopher L., Yu, Jodie, Roth, Christopher B., Chang, Geoffrey

    “…ATP-binding cassette (ABC) transporters are integral membrane proteins that translocate a wide variety of substrates across cellular membranes and are…”
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    Journal Article
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    A Specific Cholesterol Binding Site Is Established by the 2.8 Å Structure of the Human β2-Adrenergic Receptor by Hanson, Michael A., Cherezov, Vadim, Griffith, Mark T., Roth, Christopher B., Jaakola, Veli-Pekka, Chien, Ellen Y.T., Velasquez, Jeffrey, Kuhn, Peter, Stevens, Raymond C.

    Published in Structure (London) (01-06-2008)
    “…The role of cholesterol in eukaryotic membrane protein function has been attributed primarily to an influence on membrane fluidity and curvature. We present…”
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    Journal Article
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    Structure of MsbA from E. coli: A Homolog of the Multidrug Resistance ATP Binding Cassette (ABC) Transporters by Chang, Geoffrey, Roth, Christopher B.

    “…Multidrug resistance (MDR) is a serious medical problem and presents a major challenge to the treatment of disease and the development of novel therapeutics…”
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    Journal Article
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    Analysis of full and partial agonists binding to β2-adrenergic receptor suggests a role of transmembrane helix V in agonist-specific conformational changes by Katritch, Vsevolod, Reynolds, Kimberly A., Cherezov, Vadim, Hanson, Michael A., Roth, Christopher B., Yeager, Mark, Abagyan, Ruben

    Published in Journal of molecular recognition (01-07-2009)
    “…The 2.4 Å crystal structure of the β2‐adrenergic receptor (β2AR) in complex with the high‐affinity inverse agonist (−)‐carazolol provides a detailed structural…”
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    Journal Article
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    Stabilization of the Human β 2-Adrenergic Receptor TM4–TM3–TM5 Helix Interface by Mutagenesis of Glu122 3.41, A Critical Residue in GPCR Structure by Roth, Christopher B., Hanson, Michael A., Stevens, Raymond C.

    Published in Journal of molecular biology (2008)
    “…G protein-coupled receptor (GPCR) instability represents one of the most profound obstacles in the structural study of GPCRs that bind diffusible ligands. The…”
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    Journal Article
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    Structural Basis for Allosteric Regulation of GPCRs by Sodium Ionsa by Liu, Wei, Chun, Eugene, Thompson, Aaron A., Chubukov, Pavel, Xu, Fei, Katritch, Vsevolod, Han, Gye Won, Roth, Christopher B., Heitman, Laura H., IJzerman, Adriaan P., Cherezov, Vadim, Stevens, Raymond C.

    “…Pharmacological responses of G protein-coupled receptors (GPCRs) can be fine-tuned by allosteric modulators. Structural studies of such effects have been…”
    Get full text
    Journal Article
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    Analysis of full and partial agonists binding to β 2 ‐adrenergic receptor suggests a role of transmembrane helix V in agonist‐specific conformational changes by Katritch, Vsevolod, Reynolds, Kimberly A., Cherezov, Vadim, Hanson, Michael A., Roth, Christopher B., Yeager, Mark, Abagyan, Ruben

    Published in Journal of molecular recognition (01-07-2009)
    “…The 2.4 Å crystal structure of the β 2 ‐adrenergic receptor ( β 2 AR) in complex with the high‐affinity inverse agonist (−)‐carazolol provides a detailed…”
    Get full text
    Journal Article
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    A specific cholesterol binding site is established by the 2.8 Å structure of the human β2-adrenergic receptor in an alternate crystal form by Hanson, Michael A., Cherezov, Vadim, Roth, Christopher B., Griffith, Mark T., Jaakola, Veli-Pekka, Chien, Ellen Y. T., Velasquez, Jeffrey, Kuhn, Peter, Stevens, Raymond C.

    Published in Structure (London) (01-06-2008)
    “…The role of cholesterol in eukaryotic membrane protein function has been primarily attributed to an influence on membrane fluidity and curvature. Herein, we…”
    Get full text
    Journal Article
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    A specific cholesterol binding site is established by the 2.8 A structure of the human beta2-adrenergic receptor by Hanson, Michael A, Cherezov, Vadim, Griffith, Mark T, Roth, Christopher B, Jaakola, Veli-Pekka, Chien, Ellen Y T, Velasquez, Jeffrey, Kuhn, Peter, Stevens, Raymond C

    Published in Structure (London) (01-06-2008)
    “…The role of cholesterol in eukaryotic membrane protein function has been attributed primarily to an influence on membrane fluidity and curvature. We present…”
    Get full text
    Journal Article
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    Stabilization of the human beta2-adrenergic receptor TM4-TM3-TM5 helix interface by mutagenesis of Glu122(3.41), a critical residue in GPCR structure by Roth, Christopher B, Hanson, Michael A, Stevens, Raymond C

    Published in Journal of molecular biology (07-03-2008)
    “…G protein-coupled receptor (GPCR) instability represents one of the most profound obstacles in the structural study of GPCRs that bind diffusible ligands. The…”
    Get full text
    Journal Article
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    β-adrenergic receptor stability engineering for the advancement of GPCR structural biology by Roth, Christopher B

    Published 01-01-2008
    “…G-protein-coupled receptors (GPCRs) are the largest family of cell-surface receptors, accounting for >1% of the human genome and are the target of more than…”
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    Dissertation