De novo design of helical bundles as models for understanding protein folding and function

被引:273
作者
Hill, RB
Raleigh, DP
Lombardi, A
Degrado, WF [1 ]
机构
[1] Univ Penn, Johnson Res Fdn, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
[2] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
[3] Univ Naples Federico II, Dept Chem, I-80134 Naples, Italy
关键词
D O I
10.1021/ar970004h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
De novo protein design has proven to be a powerful tool for understanding protein folding, structure, and function. In this Account, we highlight aspects of our research on the design of dimeric, four-helix bundles. Dimeric, four-helix bundles are found throughout nature, and the history of their design in our laboratory illustrates our hierarchic approach to protein design. This approach has been successfully applied to create a completely native-like protein. Structural and mutational analysis allowed us to explore the determinants of native protein structure. These determinants were then applied to the design of a dinuclear metal-binding protein that can now serve as a model for this important class of proteins.
引用
收藏
页码:745 / 754
页数:10
相关论文
共 122 条
  • [1] Active barnase variants with completely random hydrophobic cores
    Axe, DD
    Foster, NW
    Fersht, AR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (11) : 5590 - 5594
  • [2] Baltzer L, 1998, BIOPOLYMERS, V47, P31, DOI 10.1002/(SICI)1097-0282(1998)47:1<31::AID-BIP5>3.3.CO
  • [3] 2-Q
  • [4] Functionalization of designed folded polypeptides
    Baltzer, L
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 1998, 8 (04) : 466 - 470
  • [5] STRUCTURE OF THE CO1E1 ROP PROTEIN AT 1.7 A RESOLUTION
    BANNER, DW
    KOKKINIDIS, M
    TSERNOGLOU, D
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1987, 196 (03) : 657 - 675
  • [6] Controlling topology and native-like behavior of de novo-designed peptides: Design and characterization of antiparallel four-stranded coiled coils
    Betz, SF
    DeGrado, WF
    [J]. BIOCHEMISTRY, 1996, 35 (21) : 6955 - 6962
  • [7] DE-NOVO PROTEIN DESIGN - FROM MOLTEN GLOBULES TO NATIVE-LIKE STATES
    BETZ, SF
    RALEIGH, DP
    DEGRADO, WF
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 1993, 3 (04) : 601 - 610
  • [8] De novo design of native proteins: Characterization of proteins intended to fold into antiparallel, rop-like, four-helix bundles
    Betz, SF
    Liebman, PA
    DeGrado, WF
    [J]. BIOCHEMISTRY, 1997, 36 (09) : 2450 - 2458
  • [9] Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis
    Booth, DR
    Sunde, M
    Bellotti, V
    Robinson, CV
    Hutchinson, WL
    Fraser, PE
    Hawkins, PN
    Dobson, CM
    Radford, SE
    Blake, CCF
    Pepys, MB
    [J]. NATURE, 1997, 385 (6619) : 787 - 793
  • [10] Selective recognition and cleavage of RNA loop structures by Ni(II)•Xaa-Gly-His metallopeptides
    Brittain, IJ
    Huang, XF
    Long, EC
    [J]. BIOCHEMISTRY, 1998, 37 (35) : 12113 - 12120