A Survey of λ Repressor Fragments from Two-State to Downhill Folding

被引:32
作者
Liu, Feng [1 ]
Gao, Yi Gui [2 ]
Gruebele, Martin [1 ,2 ,3 ]
机构
[1] Univ Illinois, Ctr Biophys & Computat Biol, Urbana, IL 61801 USA
[2] Univ Illinois, Sch Chem Sci, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Chem & Phys, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
heat denaturation; cold denaturation; CD; fluorescence; temperature jump; SPEED LIMIT; CRYSTAL-STRUCTURE; ENERGY LANDSCAPE; HYDROPHOBIC CORE; PROTEIN; KINETICS; TRANSITION; STABILITY; STATES; TEMPERATURE;
D O I
10.1016/j.jmb.2010.01.071
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We survey the two-state to downhill folding transition by examining 20 lambda(6-85)* mutants that cover a wide range of stabilities and folding rates. We investigated four new lambda(6-85)* mutants designed to fold especially rapidly. Two were engineered using the core remodeling of Lim and Sauer, and two were engineered using Ferreiro et al.'s frustratometer. These proteins have probe-dependent melting temperatures as high as 80 degrees C and exhibit a fast molecular phase with the characteristic temperature dependence of the amplitude expected for downhill folding. The survey reveals a correlation between melting temperature and downhill folding previously observed for the beta-sheet protein WW domain. A simple model explains this correlation and predicts the melting temperature at which downhill folding becomes possible. An X-ray crystal structure with a 1.64-angstrom resolution of a fast-folding mutant fragment shows regions of enhanced rigidity compared to the full wild-type protein. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:789 / 798
页数:10
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