Literature DB >> 33145813

MEMBRANE PROTEIN STRUCTURES AND INTERACTIONS FROM COVALENT LABELING COUPLED WITH MASS SPECTROMETRY.

Xiao Pan1, Richard W Vachet1.   

Abstract

Membrane proteins are incredibly important biomolecules because they mediate interactions between a cell's external and internal environment. Obtaining information about membrane protein structure and interactions is thus important for understanding these essential biomolecules. Compared with the analyses of water-soluble proteins, the structural analysis of membrane proteins is more challenging owing to their unique chemical properties and the presence of lipid components that are necessary to solubilize them. The combination of covalent labeling (CL) and mass spectrometry (MS) has recently been applied with great success to study membrane protein structure and interactions. These studies have demonstrated the many advantages that CL-MS methods have over other traditional biophysical techniques. In this review, we discuss both amino acid-specific and non-specific labeling approaches and the special considerations needed to address the unique challenges associated with interrogating membrane proteins. This review highlights the aspects of this approach that require special care to be applied correctly and provides a comprehensive review of the membrane protein systems that have been studied by CL-MS.
© 2020 John Wiley & Sons Ltd. Mass Spec Rev. © 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  covalent labeling; diethylpyrocarbonate; fast photochemical oxidation of proteins; higher-order structure; hydroxyl radical; mass spectrometry; membrane protein interactions; membrane protein structural analysis; membrane proteins

Mesh:

Substances:

Year:  2020        PMID: 33145813      PMCID: PMC8093322          DOI: 10.1002/mas.21667

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  93 in total

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5.  Radiolytic modification and reactivity of amino acid residues serving as structural probes for protein footprinting.

Authors:  Guozhong Xu; Mark R Chance
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Review 6.  Implementing fast photochemical oxidation of proteins (FPOP) as a footprinting approach to solve diverse problems in structural biology.

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Journal:  Methods       Date:  2018-05-23       Impact factor: 3.608

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9.  Chemical Penetration Enhancers Increase Hydrogen Peroxide Uptake in C. elegans for In Vivo Fast Photochemical Oxidation of Proteins.

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10.  Implementing In-Cell Fast Photochemical Oxidation of Proteins in a Platform Incubator with a Movable XY Stage.

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