HSP90 at the hub of protein homeostasis: emerging mechanistic insights

被引:1381
作者
Taipale, Mikko [1 ]
Jarosz, Daniel F. [1 ,2 ]
Lindquist, Susan [1 ,2 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Howard Hughes Med Inst, Dept Biol, Cambridge, MA 02139 USA
关键词
HEAT-SHOCK-PROTEIN; MOLECULAR CHAPERONE HSP90; VIRUS TRANSFORMING PROTEIN; ESCHERICHIA-COLI HSP90; 7-AMINO ACID SEQUENCE; NITRIC-OXIDE SYNTHASE; N-TERMINAL DOMAIN; ATPASE ACTIVITY; GLUCOCORTICOID-RECEPTOR; CRYSTAL-STRUCTURE;
D O I
10.1038/nrm2918
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heat shock protein 90 (HSP90) is a highly conserved molecular chaperone that facilitates the maturation of a wide range of proteins (known as clients). Clients are enriched in signal transducers, including kinases and transcription factors. Therefore, HSP90 regulates diverse cellular functions and exerts marked effects on normal biology, disease and evolutionary processes. Recent structural and functional analyses have provided new insights on the transcriptional and biochemical regulation of HSP90 and the structural dynamics it uses to act on a diverse client repertoire. Comprehensive understanding of how HSP90 functions promises not only to provide new avenues for therapeutic intervention, but to shed light on fundamental biological questions.
引用
收藏
页码:515 / 528
页数:14
相关论文
共 177 条
  • [11] THE SPECIFIC INTERACTION OF THE ROUS-SARCOMA VIRUS TRANSFORMING PROTEIN, PP60SRC, WITH 2 CELLULAR PROTEINS
    BRUGGE, JS
    ERIKSON, E
    ERIKSON, RL
    [J]. CELL, 1981, 25 (02) : 363 - 372
  • [12] BRUGGE JS, 1986, CURR TOP MICROBIOL, V123, P1
  • [13] Molecular chaperones and protein kinase quality control
    Caplan, Avrom J.
    Mandal, Atin K.
    Theodoraki, Maria A.
    [J]. TRENDS IN CELL BIOLOGY, 2007, 17 (02) : 87 - 92
  • [14] Dimerization and N-terminal domain proximity underlie the function of the molecular chaperone heat shock protein 90
    Chadli, A
    Bouhouche, I
    Sullivan, W
    Stensgard, B
    McMahon, N
    Catelli, MG
    Toft, DO
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) : 12524 - 12529
  • [15] Comparative genomics and evolution of the HSP90 family of genes across all kingdoms of organisms
    Chen, Bin
    Zhong, Daibin
    Monteiro, Antonia
    [J]. BMC GENOMICS, 2006, 7 (1)
  • [16] The Hsp90 chaperone complex regulates GDI-dependent rab recycling
    Chen, Christine Y.
    Balch, William E.
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (08) : 3494 - 3507
  • [17] Defining the requirements for Hsp40 and Hsp70 in the Hsp90 chaperone pathway
    Cintron, Nela S.
    Toft, David
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (36) : 26235 - 26244
  • [18] Hsp90 recognizes a common surface on client kinases
    Citri, Ami
    Harari, Daniel
    Shohat, Galit
    Ramakrishnan, Parameswaran
    Gan, Judith
    Lavi, Sara
    Eisenstein, Miriam
    Kimchi, Adi
    Wallach, David
    Pietrokovski, Shmuel
    Yarden, Yosef
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (20) : 14361 - 14369
  • [19] The co-chaperone CHIP regulates protein triage decisions mediated by heat-shock proteins
    Connell, P
    Ballinger, CA
    Jiang, JH
    Wu, YX
    Thompson, LJ
    Höhfeld, J
    Patterson, C
    [J]. NATURE CELL BIOLOGY, 2001, 3 (01) : 93 - 96
  • [20] Hsp90 potentiates the rapid evotution of new traits: Drug resistance in diverse fungi
    Cowen, LE
    Lindquist, S
    [J]. SCIENCE, 2005, 309 (5744) : 2185 - 2189