Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2001 Nov 5;2(11):798-808.
doi: 10.1002/1439-7633(20011105)2:11<798::AID-CBIC798>3.0.CO;2-L.

Scanning force microscopy of artificial membranes

Affiliations
Review

Scanning force microscopy of artificial membranes

A Janshoff et al. Chembiochem. .

Abstract

Visualization of biological membranes by scanning force microscopy (SFM) has tremendously improved the current understanding of protein-lipid interactions under physiological conditions. SFM is the only tool to directly image processes on surfaces in aqueous solution at molecular resolution. Besides being a supportive means to confirm results on lipid phases and domains obtained from fluorescence spectroscopy, calorimetry, and X-ray crystallography, SFM has contributed distinct aspects on the formation of 2D crystals of various membrane-confined proteins and morphological changes of membranes due to the interaction of peptides and proteins. This review will focus on recent results in SFM imaging of artificial solid-supported membranes, their phase behavior as a response to the environment, and changes in membrane morphology induced by the partitioning of peptides and proteins.

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources