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Influence of the extracellular domain size on the dynamic behavior of membrane proteins.
Gurdap, Cenk Onur; Wedemann, Linda; Sych, Taras; Sezgin, Erdinc.
Afiliação
  • Gurdap CO; Science for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.
  • Wedemann L; Science for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.
  • Sych T; Science for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.
  • Sezgin E; Science for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden. Electronic address: erdinc.sezgin@ki.se.
Biophys J ; 121(20): 3826-3836, 2022 10 18.
Article em En | MEDLINE | ID: mdl-36110044
The dynamic behavior of plasma membrane proteins mediates various cellular processes such as cellular motility, communication, and signaling. It is widely accepted that the dynamics of the membrane proteins is determined either by the interactions of the transmembrane domain with the surrounding lipids or by the interactions of the intracellular domain with cytosolic components such as cortical actin. Although initiation of different cellular signaling events at the plasma membrane has been attributed to the extracellular domain (ECD) properties recently, the impact of ECDs on the dynamic behavior of membrane proteins is rather unexplored. Here, we investigate how ECD properties influence protein dynamics in the lipid bilayer by reconstituting ECDs of different sizes or glycosylation in model membrane systems and analyzing ECD-driven protein sorting in lipid domains as well as protein mobility. Our data show that increasing the ECD mass or glycosylation leads to a decrease in ordered domain partitioning and diffusivity. Our data reconcile different mechanisms proposed for the initiation of cellular signaling by linking the ECD size of membrane proteins with their localization and diffusion dynamics in the plasma membrane.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bicamadas Lipídicas / Proteínas de Membrana Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bicamadas Lipídicas / Proteínas de Membrana Idioma: En Ano de publicação: 2022 Tipo de documento: Article