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Stephen J. Coales

Researcher at GlaxoSmithKline

Publications -  23
Citations -  1367

Stephen J. Coales is an academic researcher from GlaxoSmithKline. The author has contributed to research in topics: Hydrogen–deuterium exchange & Mass spectrometry. The author has an hindex of 17, co-authored 22 publications receiving 1260 citations.

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Specificity of immobilized porcine pepsin in H/D exchange compatible conditions

TL;DR: While the specificity of pepsin was similar to that previously observed, higher selectivity was observed in the present study due to less experimental variation in the conditions used to generate the database.
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Structure and dynamics of NBD1 from CFTR characterized using crystallography and hydrogen/deuterium exchange mass spectrometry.

TL;DR: The results reinforce the importance of the perturbation DeltaF508 causes in the surface topography of NBD1 in a region likely to mediate contact with the transmembrane domains of CFTR, and suggest that increased exposure of the 509-511 loop and increased dynamics in its vicinity could promote aggregation in vitro and aberrant intermolecular interactions that impede trafficking in vivo.
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Hydrogen/deuterium-exchange (H/D-Ex) of PPARγ LBD in the presence of various modulators

TL;DR: The results showed that the change in protein dynamics induced by ligand binding may be an important factor for the activation of genes and that H/D‐Ex is a useful method for analyzing the biological activity of drug leads.
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Epitope mapping by amide hydrogen/deuterium exchange coupled with immobilization of antibody, on-line proteolysis, liquid chromatography and mass spectrometry.

TL;DR: The epitope of horse cytochrome c against monoclonal antibody E8 was determined using amide hydrogen/deuterium (H/D) exchange combined with immobilized antibody, on-line pepsin proteolysis, liquid chromatography (LC), and mass spectrometry (MS).
Journal Article

Rapid Analysis of Protein Structure and Dynamics by Hydrogen/Deuterium Exchange Mass Spectrometry

TL;DR: Improvements in the amide H/D-Ex methodology described here include solid phase proteolysis, automated liquid handling and sample preparation, and integrated data reduction software that together improve sequence coverage and resolution, while achieving a sample throughput nearly 10-fold higher than the commonly used manual methods.