Single-Molecule Imaging of the H-Ras Membrane-Anchor Reveals Domains in the Cytoplasmic Leaflet of the Cell Membrane

Piet H.M. Lommerse, Gerhard A. Blab, Laurent Cognet, Gregory S. Harms, B. Ewa Snaar-Jagalska, Herman P. Spaink, Thomas Schmidt*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

In the last decade evidence has accumulated that small domains of 50-700 nm in diameter are located in the exoplasmic leaflet of the plasma membrane. Most of these domains supposedly consist of specific sets of lipids and proteins, and are believed to coordinate signal transduction cascades. Whether similar domains are also present in the cytoplasmic leaflet of the plasma membrane is unclear so far. To investigate the presence of cytoplasmic leaflet domains, the H-Ras membrane-targeting sequence was fused to the C-terminus of the enhanced yellow fluorescent protein. Using single-molecule fluorescence microscopy, trajectories of individual molecules diffusing in the cytoplasmic leaflet of the plasma membrane were recorded. From these trajectories, the diffusion of individual membrane-anchored enhanced yellow fluorescent protein molecules was studied in live cells on timescales from 5 to 200 ms. The results show that the diffusion of 30-40% of the molecules is constrained in domains with a typical size of 200 nm. Neither breakdown of actin nor cholesterol extraction changed the domain characteristics significantly, indicating that the observed domains may not be related to the membrane domains identified so far.

Original languageEnglish
Pages (from-to)609-616
Number of pages8
JournalBiophysical Journal
Volume86
Issue number1 I
DOIs
Publication statusPublished - Jan 2004

Bibliographical note

Funding Information:
This work was supported by funds from the ALW/FOM program for Physical Biology (99FBK03) of the Nederlands Organisation voor Wetensdupelijk Onderzoek. L.C. acknowledges support from the Délégation General pour l’Armement and the European Marie-Curie fellowship program (IHP-MCFI-1999-00736).

Funding

This work was supported by funds from the ALW/FOM program for Physical Biology (99FBK03) of the Nederlands Organisation voor Wetensdupelijk Onderzoek. L.C. acknowledges support from the Délégation General pour l’Armement and the European Marie-Curie fellowship program (IHP-MCFI-1999-00736).

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