Unit
UNIT 28.3 Circular Dichroism in Protein Folding Studies
Published Online: 1 NOV 2012
DOI: 10.1002/0471140864.ps2803s70
Copyright © 2012 by John Wiley & Sons, Inc.
Lab Protocol Title

Current Protocols in Protein Science
Additional Information
How to Cite
Clarke, D. T. 2012. Circular Dichroism in Protein Folding Studies. Current Protocols in Protein Science. 70:28.3:28.3.1–28.3.17.
Publication History
- Published Online: 1 NOV 2012
- Published Print: NOV 2012
- Abstract
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Abstract
Protein folding is a biological process of both fundamental significance and practical importance, and protein misfolding is implicated in a number of serious diseases of both humans and animals. The study of protein folding requires a technique that is able to monitor changes in protein structure in solution, with millisecond time resolution. Ultraviolet circular dichroism (CD) is such a technique, providing information on both secondary and tertiary protein structure. This unit describes the procedures for performing CD experiments for the study of protein folding, and identifies commonly encountered problems and their solutions. Curr. Protoc. Protein Sci. 70:28.3.1-28.3.17. © 2012 by John Wiley & Sons, Inc.
Keywords:
- protein folding;
- circular dichroism;
- stopped-flow;
- protein structure
