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

被引:88
作者
Greenfield, Norma J. [1 ]
机构
[1] Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ 08854 USA
关键词
D O I
10.1038/nprot.2006.244
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2891 / 2899
页数:9
相关论文
共 61 条
[1]  
Anfinsen C B, 1975, Adv Protein Chem, V29, P205, DOI 10.1016/S0065-3233(08)60413-1
[2]  
BALDWIN RL, 1995, J BIOMOL NMR, V5, P103
[3]   INTERMEDIATES IN PROTEIN FOLDING REACTIONS AND MECHANISM OF PROTEIN FOLDING [J].
BALDWIN, RL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1975, 44 :453-475
[4]  
Baum Jean, 1999, Current Opinion in Structural Biology, V9, P122, DOI 10.1016/S0959-440X(99)80016-5
[5]   PHYSICAL EVIDENCE FOR THE ASSEMBLY OF A-CHAINS AND B-CHAINS OF HUMAN PLACENTAL COLLAGEN IN A SINGLE TRIPLE HELIX [J].
BENTZ, H ;
BACHINGER, HP ;
GLANVILLE, R ;
KUHN, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1978, 92 (02) :563-567
[6]   Nucleation and propagation of the collagen triple helix in single-chain and trimerized peptides:: Transition from third to first order kinetics [J].
Boudko, S ;
Frank, S ;
Kammerer, RA ;
Stetefeld, J ;
Schulthess, T ;
Landwehr, R ;
Lustig, A ;
Bächinger, HP ;
Engel, J .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 317 (03) :459-470
[7]   CIRCULAR DICHROISM SPECTRUM OF POLY-L-PROLINE [J].
BOVEY, FA ;
HOOD, FP .
BIOPOLYMERS, 1967, 5 (03) :325-&
[8]   Polyglutamine aggregation behavior in vitro supports a recruitment mechanism of cytotoxicity [J].
Chen, S ;
Berthelier, V ;
Yang, W ;
Wetzel, R .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 311 (01) :173-182
[9]   Protein misfolding, functional amyloid, and human disease [J].
Chiti, Fabrizio ;
Dobson, Christopher M. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :333-366
[10]   PARTIAL DENATURATION OF TRANSTHYRETIN IS SUFFICIENT FOR AMYLOID FIBRIL FORMATION INVITRO [J].
COLON, W ;
KELLY, JW .
BIOCHEMISTRY, 1992, 31 (36) :8654-8660