Periprotein lipidomes of


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
17 04 2020
Historique:
received: 17 03 2020
accepted: 09 04 2020
pubmed: 18 4 2020
medline: 10 4 2021
entrez: 18 4 2020
Statut: epublish

Résumé

Yeast tolerates a low pH and high solvent concentrations. The permeability of the plasma membrane (PM) for small molecules is low and lateral diffusion of proteins is slow. These findings suggest a high degree of lipid order, which raises the question of how membrane proteins function in such an environment. The yeast PM is segregated into the Micro-Compartment-of-Can1 (MCC) and Pma1 (MCP), which have different lipid compositions. We extracted proteins from these microdomains via stoichiometric capture of lipids and proteins in styrene-maleic-acid-lipid-particles (SMALPs). We purified SMALP-lipid-protein complexes by chromatography and quantitatively analyzed periprotein lipids located within the diameter defined by one SMALP. Phospholipid and sterol concentrations are similar for MCC and MCP, but sphingolipids are enriched in MCP. Ergosterol is depleted from this periprotein lipidome, whereas phosphatidylserine is enriched relative to the bulk of the plasma membrane. Direct detection of PM lipids in the 'periprotein space' supports the conclusion that proteins function in the presence of a locally disordered lipid state.

Identifiants

pubmed: 32301705
doi: 10.7554/eLife.57003
pii: 57003
pmc: PMC7182430
doi:
pii:

Substances chimiques

Membrane Lipids 0
Membrane Proteins 0
Phospholipids 0
Saccharomyces cerevisiae Proteins 0
Sphingolipids 0
Sterols 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR048632
Pays : United States
Organisme : NIH HHS
ID : AR048632
Pays : United States
Organisme : European Research Council
ID : 670578
Pays : International

Déclaration de conflit d'intérêts

Jv, TC, HS, AJ, BM, BP No competing interests declared

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Auteurs

Joury S van 't Klooster (JS)

Department of Biochemistry, University of Groningen Groningen Biomolecular Sciences and Biotechnology Institute, Groningen, Netherlands.

Tan-Yun Cheng (TY)

Division of Rheumatology, Inflammation and Immunity Brigham and Women's Hospital, Harvard Medical School, Boston, United States.

Hendrik R Sikkema (HR)

Department of Biochemistry, University of Groningen Groningen Biomolecular Sciences and Biotechnology Institute, Groningen, Netherlands.

Aike Jeucken (A)

Department of Biochemistry, University of Groningen Groningen Biomolecular Sciences and Biotechnology Institute, Groningen, Netherlands.

Branch Moody (B)

Division of Rheumatology, Inflammation and Immunity Brigham and Women's Hospital, Harvard Medical School, Boston, United States.
Department of Medicine, Harvard Medical School, Boston, United States.

Bert Poolman (B)

Department of Biochemistry, University of Groningen Groningen Biomolecular Sciences and Biotechnology Institute, Groningen, Netherlands.

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