Polar group burial contributes more to protein stability than nonpolar group burial

被引:122
作者
Pace, CN [1 ]
机构
[1] Texas A&M Univ, Dept Biochem Med, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Genet, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
[4] Texas A&M Univ, Ctr Adv Biomol Res, College Stn, TX 77843 USA
关键词
D O I
10.1021/bi001574j
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
On the basis of studies of Asn to Ala mutants, the gain in stability from burying amide groups that are hydrogen bonded to peptide groups is 80 cal/(mol Angstrom (3)). On the basis of similar studies of Leu to Ala and Ile to Val mutants, the gain in stability from burying -CH2- groups is 50 cal/(mol Angstrom (3)). Thus, the burial of an amide group contributes more to protein stability than the burial of an equivalent volume of -CH2-groups. Applying these results to folded proteins leads to the surprising conclusion that peptide group burial makes a larger contribution to protein stability than nonpolar side chain burial. Several studies have shown that the desolvation penalty for burying peptide groups is considerably smaller than generally thought. This suggests that the hydrogen bonding and van der Waals interactions of peptide groups in the tightly packed interior of folded protein are mon favorable than similar interactions with water in the unfolded protein.
引用
收藏
页码:310 / 313
页数:4
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