Mass Spectrometry Reveals the Direct Action of a Chemical Chaperone
Author(s) -
Joseph Gault,
Danai Lianoudaki,
Margit Kaldmäe,
Nina Kronqvist,
Anna Rising,
Jan Johansson,
Bernhard Lohkamp,
Sonia Laı́n,
Timothy M. Allison,
David P. Lane,
Erik G. Marklund,
Michael Landreh
Publication year - 2018
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.8b01817
Subject(s) - mass spectrometry , chaperone (clinical) , chemistry , computational biology , biology , chromatography , medicine , pathology
Despite their fundamental biological importance and therapeutic potential, the interactions between chemical chaperones and proteins remain difficult to capture due to their transient and nonspecific nature. Using a simple mass spectrometric assay, we are able to follow the interactions between proteins and the chemical chaperone trimethylamine- N-oxide (TMAO). In this manner, we directly observe that the counteraction of TMAO and the denaturant urea is driven by the exclusion of TMAO from the protein surface, whereas the surfactant lauryl dimethylamine- N-oxide cannot be displaced. Our results clearly demonstrate a direct chaperoning mechanism for TMAO, corroborating extensive computational studies, and pave the way for the use of nondenaturing mass spectrometry and related techniques to study chemical chaperones in molecular detail.
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