Literature DB >> 17406548

Analysis of the kinetics of folding of proteins and peptides using circular dichroism.

Norma J Greenfield1.   

Abstract

Circular dichroism (CD) is a useful spectroscopic technique for studying the secondary structure, folding and binding properties of proteins. This protocol covers how to use the intrinsic circular dichroic properties of proteins to follow their folding and unfolding as a function of time. Included are methods of obtaining data and for analyzing the folding and unfolding data to determine the rate constants and the order of the folding and unfolding reactions. The protocol focuses on the use of CD to follow folding when it is relatively slow, on the order of minutes to days. The methods for analyzing the data, however, can also be applied to data collected with a CD machine equipped with stopped-flow accessories in the range of milliseconds to seconds and folding analyzed by other spectroscopic methods including changes in absorption or fluorescence spectra as a function of time.

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Year:  2006        PMID: 17406548      PMCID: PMC2752309          DOI: 10.1038/nprot.2006.244

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  55 in total

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Journal:  Annu Rev Phys Chem       Date:  1996       Impact factor: 12.703

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Journal:  Biochemistry       Date:  1996-05-14       Impact factor: 3.162

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Journal:  Methods Enzymol       Date:  1997       Impact factor: 1.600

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Authors:  K Kuwajima
Journal:  Methods Mol Biol       Date:  1995

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Authors:  C A Royer
Journal:  Methods Mol Biol       Date:  1995

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Authors:  R L Baldwin
Journal:  J Biomol NMR       Date:  1995-02       Impact factor: 2.835

7.  Probing the folding mechanism of a leucine zipper peptide by stopped-flow circular dichroism spectroscopy.

Authors:  J A Zitzewitz; O Bilsel; J Luo; B E Jones; C R Matthews
Journal:  Biochemistry       Date:  1995-10-03       Impact factor: 3.162

8.  Characterization of collagen-like peptides containing interruptions in the repeating Gly-X-Y sequence.

Authors:  C G Long; E Braswell; D Zhu; J Apigo; J Baum; B Brodsky
Journal:  Biochemistry       Date:  1993-11-02       Impact factor: 3.162

9.  Partial denaturation of transthyretin is sufficient for amyloid fibril formation in vitro.

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Authors:  J Hope; M S Shearman; H C Baxter; A Chong; S M Kelly; N C Price
Journal:  Neurodegeneration       Date:  1996-03
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  34 in total

1.  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

2.  Using circular dichroism spectra to estimate protein secondary structure.

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

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6.  Membrane requirement for folding of the herpes simplex virus 1 gB cytodomain suggests a unique mechanism of fusion regulation.

Authors:  Jessica L Silverman; Neil G Greene; David S King; Ekaterina E Heldwein
Journal:  J Virol       Date:  2012-05-23       Impact factor: 5.103

7.  A molecular interpretation of 2D IR protein folding experiments with Markov state models.

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8.  Antioxidant capacity and structural changes of human serum albumin from patients in advanced stages of diabetic nephropathy and the effect of the dialysis.

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9.  Combinatorial active-site variants confer sustained clavulanate resistance in BlaC β-lactamase from Mycobacterium tuberculosis.

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10.  Contributions of different modules of the plasminogen-binding Streptococcus pyogenes M-protein that mediate its functional dimerization.

Authors:  Cunjia Qiu; Yue Yuan; Jaroslav Zajicek; Zhong Liang; Rashna D Balsara; Teresa Brito-Robionson; Shaun W Lee; Victoria A Ploplis; Francis J Castellino
Journal:  J Struct Biol       Date:  2018-07-30       Impact factor: 2.867

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