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

NJ Greenfield - Nature protocols, 2006 - nature.com
Nature protocols, 2006nature.com
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 …
Abstract
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.
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