Literature DB >> 15064449

Circular dichroism analysis for protein-protein interactions.

Norma J Greenfield1.   

Abstract

Circular dichroism (CD) spectroscopy is a useful technique for studying protein-protein interactions in solution. CD in the far ultraviolet region (178-260 nm) arises from the amides of the protein backbone and is sensitive to the conformation of the protein. Thus CD can determine whether there are changes in the conformation of proteins when they interact. CD bands in the near ultraviolet (350-260 nm) and visible regions arise from aromatic and prosthetic groups. There are also changes in these regions when proteins bind to each other. Because CD is a quantitative technique, changes in CD spectra are directly proportional to the amount of the protein-protein complexes formed, and these changes can be used to estimate binding constants. Changes in the stability of the protein complexes as a function of temperature or added denaturants, compared to the isolated proteins, can also be used to determine binding constants.

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Year:  2004        PMID: 15064449     DOI: 10.1385/1-59259-762-9:055

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  23 in total

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Authors:  Sarah E Wilkins; Sarah Karttunen; Rachel J Hampton-Smith; Iain Murchland; Anne Chapman-Smith; Daniel J Peet
Journal:  J Biol Chem       Date:  2012-01-23       Impact factor: 5.157

Review 2.  Diversity in genetic in vivo methods for protein-protein interaction studies: from the yeast two-hybrid system to the mammalian split-luciferase system.

Authors:  Bram Stynen; Hélène Tournu; Jan Tavernier; Patrick Van Dijck
Journal:  Microbiol Mol Biol Rev       Date:  2012-06       Impact factor: 11.056

3.  Pyruvate formate-lyase, evidence for an open conformation favored in the presence of its activating enzyme.

Authors:  Yi Peng; Susan E Veneziano; Gregory D Gillispie; Joan B Broderick
Journal:  J Biol Chem       Date:  2010-06-22       Impact factor: 5.157

4.  CcmI subunit of CcmFHI heme ligation complex functions as an apocytochrome c chaperone during c-type cytochrome maturation.

Authors:  Andreia F Verissimo; Honghui Yang; Xiaomin Wu; Carsten Sanders; Fevzi Daldal
Journal:  J Biol Chem       Date:  2011-09-28       Impact factor: 5.157

5.  Tropomodulin binds two tropomyosins: a novel model for actin filament capping.

Authors:  Alla S Kostyukova; Andy Choy; Brian A Rapp
Journal:  Biochemistry       Date:  2006-10-03       Impact factor: 3.162

6.  Using circular dichroism collected as a function of temperature to determine the thermodynamics of protein unfolding and binding interactions.

Authors:  Norma J Greenfield
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

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

Authors:  Norma J Greenfield
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

8.  Interaction of asymmetric ABCC9-encoded nucleotide binding domains determines KATP channel SUR2A catalytic activity.

Authors:  Sungjo Park; Bernard B C Lim; Carmen Perez-Terzic; Georges Mer; Andre Terzic
Journal:  J Proteome Res       Date:  2008-03-01       Impact factor: 4.466

9.  Molecular epitopes of the ankyrin-spectrin interaction.

Authors:  Jonathan J Ipsaro; Lei Huang; Lucy Gutierrez; Ruby I MacDonald
Journal:  Biochemistry       Date:  2008-06-19       Impact factor: 3.162

10.  Structure and tropomyosin binding properties of the N-terminal capping domain of tropomodulin 1.

Authors:  Norma J Greenfield; Alla S Kostyukova; Sarah E Hitchcock-DeGregori
Journal:  Biophys J       Date:  2004-10-08       Impact factor: 4.033

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