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Mass spectrometry: from plasma proteins to mitochondrial membranes

Abstract:
In this Inaugural Article, I trace some key steps that have enabled the development of mass spectrometry for the study of intact protein complexes from a variety of cellular environments. Beginning with the preservation of the first soluble complexes from plasma, I describe our early experiments that capitalize on the heterogeneity of subunit composition during assembly and exchange reactions. During these investigations, we observed many assemblies and intermediates with different subunit stoichiometries, and were keen to ascertain whether or not their overall topology was preserved in the mass spectrometer. Adapting ion mobility and soft-landing methodologies, we showed how ring-shaped complexes could survive the phase transition. The next logical progression from soluble complexes was to membrane protein assemblies but this was not straightforward. We encountered many pitfalls along the way, largely due to the use of detergent micelles to protect and stabilize complexes. Further obstacles presented when we attempted to distinguish lipids that copurify from those that are important for function. Developing new experimental protocols, we have subsequently defined lipids that change protein conformation, mediate oligomeric states, and facilitate downstream coupling of G protein-coupled receptors. Very recently, using a radical method-ejecting protein complexes directly from native membranes into mass spectrometers-we provided insights into associations within membranes and mitochondria. Together, these developments suggest the beginnings of mass spectrometry meeting with cell biology.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1073/pnas.1820450116

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Physical & Theoretical Chem
Oxford college:
Exeter College
Role:
Author
ORCID:
0000-0001-7829-5505


Publisher:
National Academy of Sciences
Journal:
Proceedings of the National Academy of Sciences More from this journal
Volume:
116
Issue:
8
Pages:
2814-2820
Publication date:
2019-02-04
Acceptance date:
2018-12-26
DOI:
EISSN:
1091-6490
ISSN:
0027-8424
Pmid:
30718422


Language:
English
Keywords:
Pubs id:
pubs:969518
UUID:
uuid:1fc40125-fa52-4f51-aac9-614bb232a585
Local pid:
pubs:969518
Source identifiers:
969518
Deposit date:
2019-06-28
ARK identifier:

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