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Updated: Jul 30, 2026

Microcontact Printing of Proteins for Cell Biology
Published on: December 5, 2008
Using liquid crystals to report membrane proteins captured by affinity microcontact printing from cell lysates and
Chang-Hyun Jang1, Matthew L Tingey, Nichole L Korpi
1Department of Chemical and Biological Engineering,University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Abstract:
The chemical heterogeneity of proteins makes development of general and facile surface-based methods for protein analysis a substantial challenge, particularly when analyzing transmembrane proteins. Here, we report a simple surface-based procedure that permits detection of transmembrane proteins from crude cell lysates and cell membrane extracts. The method relies on the use of thermotropic liquid crystals to amplify and report the presence of the transmembrane proteins captured by an affinity ligand on the surface of an elastomeric stamp. A merit of this approach is that the proteins can be imaged on surfaces without requiring the use of matched pairs of antibodies, labels, or complex instrumentation. Detection of epidermal growth factor receptor, a transmembrane glycoprotein, is demonstrated.

