Tracking Higher Order Protein Structure by Hydrogen-Deuterium Exchange Mass Spectrometry
-
Published:2019-02-13
Issue:1
Volume:26
Page:16-26
-
ISSN:0929-8665
-
Container-title:Protein & Peptide Letters
-
language:en
-
Short-container-title:PPL
Author:
Benhaim Mark1, Lee Kelly K.1, Guttman Miklos1
Affiliation:
1. Department of Medicinal Chemistry, Medicinal Chemistry Faculty, University of Washington, Seattle, WA 98195, United States
Abstract
Background:
Structural biology has provided a fundamental understanding of protein
structure and mechanistic insight into their function. However, high-resolution structures alone are
insufficient for a complete understanding of protein behavior. Higher energy conformations, conformational
changes, and subtle structural fluctuations that underlie the proper function of proteins
are often difficult to probe using traditional structural approaches. Hydrogen/Deuterium Exchange
with Mass Spectrometry (HDX-MS) provides a way to probe the accessibility of backbone amide
protons under native conditions, which reports on local structural dynamics of solution protein
structure that can be used to track complex structural rearrangements that occur in the course of a
protein’s function.
Conclusion:
In the last 20 years the advances in labeling techniques, sample preparation, instrumentation,
and data analysis have enabled HDX to gain insights into very complex biological systems.
Analysis of challenging targets such as membrane protein complexes is now feasible and the
field is paving the way to the analysis of more and more complex systems.
Funder
Bill and Melinda Gates Foundation Global health vaccine accelerator platform NIH
Publisher
Bentham Science Publishers Ltd.
Subject
Biochemistry,General Medicine,Structural Biology
Reference122 articles.
1. Englander SW. J Am Soc Mass Spectrom, Hydrogen exchange and mass spectrometry: A historical perspective.,, 2006, 17,, 1481-1489, 2. Wang G, Abzalimov RR, Bobst CE, Kaltashov IA. Proc Natl Acad Sci USA, Conformer-specific characterization of nonnative protein states using hydrogen exchange and top-down mass spectrometry.,, 2013, 110,, 20087-20092, 3. Mandell JG, Baerga-Ortiz A, Falick AM, Komives EA. Methods Mol Biol, Measurement of solvent accessibility at protein-protein interfaces.,, 2005, 305,, 65-80, 4. Marcsisin SR, Engen JR. Anal Bioanal Chem, Hydrogen exchange mass spectrometry: What is it and what can it tell us?,, 2010, 397,, 967-972, 5. Marciano DP, Dharmarajan V, Griffin PR. Curr Opin Struct Biol, HDX-MS guided drug discovery: Small molecules and biopharmaceuticals.,, 2014, 28,, 105-111,
Cited by
22 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|