Issue 24, 2015

Specific adhesion of membranes simultaneously supports dual heterogeneities in lipids and proteins

Abstract

Membrane adhesion is a vital component of many biological processes. Heterogeneities in lipid and protein composition are often associated with the adhesion site. These heterogeneities are thought to play functional roles in facilitating signalling. Here we experimentally examine this phenomenon using model membranes made of a mixture of lipids that is near a phase boundary at room temperature. Non-adherent model membranes are in a well-mixed, disordered-fluid lipid phase indicated by homogeneous distribution of a fluorescent dye that is a marker for the fluid-disordered (Ld) phase. We specifically adhere membranes to a flat substrate bilayer using biotin–avidin binding. Adhesion produces two types of coexisting heterogeneities: an ordered lipid phase that excludes binding proteins and the fluorescent membrane dye, and a disordered lipid phase that is enriched in both binding proteins and membrane dye compared with the non-adhered portion of the same membrane. Thus, a single type of adhesion interaction (biotin–avidin binding), in an initially-homogeneous system, simultaneously stabilizes both ordered-phase and disordered-phase heterogeneities that are compositionally distinct from the non-adhered portion of the vesicle. These heterogeneities are long-lived and unchanged upon increased temperature.

Graphical abstract: Specific adhesion of membranes simultaneously supports dual heterogeneities in lipids and proteins

Supplementary files

Article information

Article type
Paper
Submitted
15 Dec 2014
Accepted
27 Mar 2015
First published
02 Apr 2015

Phys. Chem. Chem. Phys., 2015,17, 15598-15607

Author version available

Specific adhesion of membranes simultaneously supports dual heterogeneities in lipids and proteins

O. Shindell, N. Mica, M. Ritzer and V. D. Gordon, Phys. Chem. Chem. Phys., 2015, 17, 15598 DOI: 10.1039/C4CP05877A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements