| Literature DB >> 31082219 |
Hongda Liu, Dawei Wang, Qiangmin Zhang, Yang Zhao, Tatyana Mamonova, Lei Wang, Cheng Zhang, Sheng Li1, Peter A Friedman, Kunhong Xiao.
Abstract
Hydrogen-deuterium exchange-mass spectrometry (HDXMS) is a powerful technology to characterize conformations and conformational dynamics of proteins and protein complexes. HDXMS has been widely used in the field of therapeutics for the development of protein drugs. Although sufficient sequence coverage is critical to the success of HDXMS, it is sometimes difficult to achieve. In this study, we developed a HDXMS data analysis strategy that includes parallel post-translational modification (PTM) scanning in HDXMS analysis. Using a membrane-delimited G protein-coupled receptor (vasopressin type 2 receptor; V2R) and a cytosolic protein (Na+/H+ exchanger regulatory factor-1; NHERF1) as examples, we demonstrate that this strategy substantially improves protein sequence coverage, especially in key structural regions likely including PTMs themselves that play important roles in protein conformational dynamics and function.Entities:
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Year: 2019 PMID: 31082219 PMCID: PMC9270701 DOI: 10.1021/acs.analchem.9b01410
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 8.008