Sorting of multiple molecular species on cell membranes.


Journal

Physical review. E
ISSN: 2470-0053
Titre abrégé: Phys Rev E
Pays: United States
ID NLM: 101676019

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 24 01 2023
accepted: 05 06 2023
medline: 20 9 2023
pubmed: 19 9 2023
entrez: 19 9 2023
Statut: ppublish

Résumé

Eukaryotic cells maintain their inner order by a hectic process of sorting and distillation of molecular factors taking place on their lipid membranes. A similar sorting process is implied in the assembly and budding of enveloped viruses. To understand the properties of this molecular sorting process, we have recently proposed a physical model [Zamparo et al., Phys. Rev. Lett. 126, 088101 (2021)]10.1103/PhysRevLett.126.088101, based on (1) the phase separation of a single, initially dispersed molecular species into spatially localized sorting domains on the lipid membrane and (2) domain-induced membrane bending leading to the nucleation of submicrometric lipid vesicles, naturally enriched in the molecules of the engulfed sorting domain. The analysis of the model showed the existence of an optimal region of parameter space where sorting is most efficient. Here the model is extended to account for the simultaneous distillation of a pool of distinct molecular species. We find that the mean time spent by sorted molecules on the membrane increases with the heterogeneity of the pool (i.e., the number of distinct molecular species sorted) according to a simple scaling law, and that a large number of distinct molecular species can in principle be sorted in parallel on cell membranes without significantly interfering with each other. Moreover, sorting is found to be most efficient when the distinct molecular species have comparable homotypic affinities. We also consider how valence (i.e., the average number of interacting neighbors of a molecule in a sorting domain) affects the sorting process, finding that higher-valence molecules can be sorted with greater efficiency than lower-valence molecules.

Identifiants

pubmed: 37723769
doi: 10.1103/PhysRevE.108.024401
doi:

Substances chimiques

Lipids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

024401

Auteurs

Andrea Piras (A)

Candiolo Cancer Institute, FPO-IRCCS, Strada Provinciale 142, km 3.95, 10060 Candiolo, Italy.
Institute of Condensed Matter Physics and Complex Systems, Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin, Italy.
Italian Institute for Genomic Medicine (IIGM), Strada Provinciale 142, km 3.95, 10060 Candiolo, Italy.
Department of Oncology, University of Turin, 10060 Candiolo, Italy.

Elisa Floris (E)

Institute of Condensed Matter Physics and Complex Systems, Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin, Italy.
Istituto Nazionale di Fisica Nucleare (INFN), Sezione di Torino, Via Pietro Giuria 1, 10125 Torino, Italy.

Luca Dall'Asta (L)

Institute of Condensed Matter Physics and Complex Systems, Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin, Italy.
Italian Institute for Genomic Medicine (IIGM), Strada Provinciale 142, km 3.95, 10060 Candiolo, Italy.
Collegio Carlo Alberto, Piazza Arbarello 8, 10122, Torino, Italy.

Andrea Gamba (A)

Institute of Condensed Matter Physics and Complex Systems, Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin, Italy.
Italian Institute for Genomic Medicine (IIGM), Strada Provinciale 142, km 3.95, 10060 Candiolo, Italy.
Istituto Nazionale di Fisica Nucleare (INFN), Sezione di Torino, Via Pietro Giuria 1, 10125 Torino, Italy.

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Classifications MeSH