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

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.

SUBMITTER: Greenfield NJ

PROVIDER: S-EPMC2728349 | biostudies-literature | 2006

REPOSITORIES: biostudies-literature

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

Greenfield Norma J NJ

Nature protocols 20060101 6

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, DN ...[more]

PMID: 17406529

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