A test of the ''jigsaw puzzle'' model for protein folding by multiple methionine substitutions within the core of T4 lysozyme

被引:135
作者
Gassner, NC [1 ]
Baase, WA [1 ]
Matthews, BW [1 ]
机构
[1] UNIV OREGON,DEPT PHYS,EUGENE,OR 97403
关键词
D O I
10.1073/pnas.93.22.12155
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To test whether the structure of a protein is determined in a manner akin to the assembly of a jigsaw puzzle, up to 10 adjacent residues within the core of T4 lysozyme were replaced by methionine. Such variants are active and fold cooperatively with progressively reduced stability, The structure of a seven-methionine variant has been shown, crystallographically, to be similar to wild type and to maintain a well ordered core. The interaction between the core residues is, therefore, not strictly comparable with the precise spatial complementarity of the pieces of a jigsaw puzzle, Rather, a certain amount of give and take in forming the core structure is permitted, A simplified hydrophobic core sequence, imposed without genetic selection or computer-based design, is sufficient to retain native properties in a globular protein.
引用
收藏
页码:12155 / 12158
页数:4
相关论文
共 29 条