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First published online on December 21, 2004.
Copyright © 2004 by The Physiological Society
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jphysiol.2004.081117v2
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Received December 13, 2004
Revised December 16, 2004
Accepted after revision December 16, 2004

Quantitative functional analysis of protein complexes on surfaces

Hye Jin Lee1, Yuling Yan2, gerard marriott3*, and Robert Corn1

1 University of California at Irvine
2 University of Hawaii
3 University of wisconsin

* To whom correspondence should be addressed. E-mail: gm{at}physiology.wisc.edu.

A major challenge in cell and molecular physiology research is to understand the mechanisms of biological processes in terms of the interactions, activities and regulation of the underlying proteins. Functional and mechanistic analyses of the large number of proteins that participate in the regulation of cellular processes will require new approaches and techniques for high throughput and multiplexed functional analyses of protein interactions, protein conformational dynamics and protein activity. In this review we focus on the development and application of proteomics and associated technologies for quantitative functional analysis of proteins and their complexes that include: (1) the application of surface plasmon resonance (SPR) imaging for multiplexed, label-free analyses of protein interactions, binding constants for biomolecular interactions and protein activities; (2) high content analysis of protein motions within functional multi-protein complexes.


Key words: Fluorescence • Kinetics







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