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Native Desorption Electrospray Ionization Liberates Soluble and Membrane Protein Complexes from Surfaces.


ABSTRACT: Mass spectrometry (MS) applications for intact protein complexes typically require electrospray (ES) ionization and have not been achieved via direct desorption from surfaces. Desorption ES ionization (DESI) MS has however transformed the study of tissue surfaces through release and characterisation of small molecules. Motivated by the desire to screen for ligand binding to intact protein complexes we report the development of a native DESI platform. By establishing conditions that preserve non-covalent interactions we exploit the surface to capture a rapid turnover enzyme-substrate complex and to optimise detergents for membrane protein study. We demonstrate binding of lipids and drugs to membrane proteins deposited on surfaces and selectivity from a mix of related agonists for specific binding to a GPCR. Overall therefore we introduce this native DESI platform with the potential for high-throughput ligand screening of some of the most challenging drug targets including GPCRs.

SUBMITTER: Ambrose S 

PROVIDER: S-EPMC5813186 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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Native Desorption Electrospray Ionization Liberates Soluble and Membrane Protein Complexes from Surfaces.

Ambrose Stephen S   Housden Nicholas G NG   Gupta Kallol K   Fan Jieyuan J   White Paul P   Yen Hsin-Yung HY   Marcoux Julien J   Kleanthous Colin C   Hopper Jonathan T S JTS   Robinson Carol V CV  

Angewandte Chemie (International ed. in English) 20170918 46


Mass spectrometry (MS) applications for intact protein complexes typically require electrospray (ES) ionization and have not been achieved via direct desorption from surfaces. Desorption ES ionization (DESI) MS has however transformed the study of tissue surfaces through release and characterisation of small molecules. Motivated by the desire to screen for ligand binding to intact protein complexes we report the development of a native DESI platform. By establishing conditions that preserve non-  ...[more]

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