Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors. / Braun, Nina; Lynagh, Timothy; Yu, Rilei; Biggin, Philip C; Pless, Stephan A.

In: A C S Chemical Neuroscience, Vol. 7, No. 3, 29.01.2016, p. 339–348.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Braun, N, Lynagh, T, Yu, R, Biggin, PC & Pless, SA 2016, 'Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors', A C S Chemical Neuroscience, vol. 7, no. 3, pp. 339–348. https://doi.org/10.1021/acschemneuro.5b00298

APA

Braun, N., Lynagh, T., Yu, R., Biggin, P. C., & Pless, S. A. (2016). Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors. A C S Chemical Neuroscience, 7(3), 339–348. https://doi.org/10.1021/acschemneuro.5b00298

Vancouver

Braun N, Lynagh T, Yu R, Biggin PC, Pless SA. Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors. A C S Chemical Neuroscience. 2016 Jan 29;7(3): 339–348. https://doi.org/10.1021/acschemneuro.5b00298

Author

Braun, Nina ; Lynagh, Timothy ; Yu, Rilei ; Biggin, Philip C ; Pless, Stephan A. / Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors. In: A C S Chemical Neuroscience. 2016 ; Vol. 7, No. 3. pp. 339–348.

Bibtex

@article{ae0e7dd2dff94913a256426026f046ae,
title = "Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors",
abstract = "Cys-loop receptors mediate fast synaptic transmission in the nervous system, and their dysfunction is associated with a number of diseases. While some sequence variability is essential to ensure specific recognition of a chemically diverse set of ligands, other parts of the underlying amino acid sequences show a high degree of conservation, possibly to preserve the overall structural fold across the protein family. In this study, we focus on the only two absolutely conserved residues across the Cys-loop receptor family, two Trp side chains in the WXD motif of Loop D and in the WXPD motif of Loop A. Using a combination of conventional mutagenesis, unnatural amino acid incorporation, immunohistochemistry and MD simulations, we demonstrate the crucial contributions of these two Trp residues to receptor expression and function in two prototypical Cys-loop receptors, the anion-selective GlyR α1 and the cation-selective nAChR α7. Specifically, our results rule out possible electrostatic contributions of these Trp side chains and instead suggest that the overall size and shape of this aromatic pair is required in stabilizing the Cys-loop receptor extracellular domain.",
author = "Nina Braun and Timothy Lynagh and Rilei Yu and Biggin, {Philip C} and Pless, {Stephan A}",
year = "2016",
month = jan,
day = "29",
doi = "10.1021/acschemneuro.5b00298",
language = "English",
volume = "7",
pages = " 339–348",
journal = "ACS Chemical Neuroscience",
issn = "1948-7193",
publisher = "American Chemical Society",
number = "3",

}

RIS

TY - JOUR

T1 - Role of an Absolutely Conserved Tryptophan Pair in the Extracellular Domain of Cys-Loop Receptors

AU - Braun, Nina

AU - Lynagh, Timothy

AU - Yu, Rilei

AU - Biggin, Philip C

AU - Pless, Stephan A

PY - 2016/1/29

Y1 - 2016/1/29

N2 - Cys-loop receptors mediate fast synaptic transmission in the nervous system, and their dysfunction is associated with a number of diseases. While some sequence variability is essential to ensure specific recognition of a chemically diverse set of ligands, other parts of the underlying amino acid sequences show a high degree of conservation, possibly to preserve the overall structural fold across the protein family. In this study, we focus on the only two absolutely conserved residues across the Cys-loop receptor family, two Trp side chains in the WXD motif of Loop D and in the WXPD motif of Loop A. Using a combination of conventional mutagenesis, unnatural amino acid incorporation, immunohistochemistry and MD simulations, we demonstrate the crucial contributions of these two Trp residues to receptor expression and function in two prototypical Cys-loop receptors, the anion-selective GlyR α1 and the cation-selective nAChR α7. Specifically, our results rule out possible electrostatic contributions of these Trp side chains and instead suggest that the overall size and shape of this aromatic pair is required in stabilizing the Cys-loop receptor extracellular domain.

AB - Cys-loop receptors mediate fast synaptic transmission in the nervous system, and their dysfunction is associated with a number of diseases. While some sequence variability is essential to ensure specific recognition of a chemically diverse set of ligands, other parts of the underlying amino acid sequences show a high degree of conservation, possibly to preserve the overall structural fold across the protein family. In this study, we focus on the only two absolutely conserved residues across the Cys-loop receptor family, two Trp side chains in the WXD motif of Loop D and in the WXPD motif of Loop A. Using a combination of conventional mutagenesis, unnatural amino acid incorporation, immunohistochemistry and MD simulations, we demonstrate the crucial contributions of these two Trp residues to receptor expression and function in two prototypical Cys-loop receptors, the anion-selective GlyR α1 and the cation-selective nAChR α7. Specifically, our results rule out possible electrostatic contributions of these Trp side chains and instead suggest that the overall size and shape of this aromatic pair is required in stabilizing the Cys-loop receptor extracellular domain.

U2 - 10.1021/acschemneuro.5b00298

DO - 10.1021/acschemneuro.5b00298

M3 - Journal article

C2 - 26764897

VL - 7

SP - 339

EP - 348

JO - ACS Chemical Neuroscience

JF - ACS Chemical Neuroscience

SN - 1948-7193

IS - 3

ER -

ID: 157061815