4.7 Article

Determination of the folding of proteins as a function of denaturants, osmolytes or ligands using circular dichroism

Journal

NATURE PROTOCOLS
Volume 1, Issue 6, Pages 2733-2741

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2006.229

Keywords

-

Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM036326] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [R01 GM036326, GM-36326, R01 GM036326-19, R01 GM036326-13] Funding Source: Medline

Ask authors/readers for more resources

Circular dichroism (CD) is an excellent tool for examining the interactions and stability of proteins. This protocol covers methods to obtain and analyze circular dichroism spectra to measure changes in the folding of proteins as a function of denaturants, osmolytes or ligands. Applications include determination of the free energy of folding of a protein, the effects of mutations on protein stability and the estimation of binding constants for the interactions of proteins with other proteins, DNA or ligands, such as substrates or inhibitors. The experiments require 2-5 h.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available