Structural biology of insulin and IGF1 receptors: Implications for drug design

被引:463
作者
De Meyts, P [1 ]
Whittaker, J [1 ]
机构
[1] Hagedorn Res Inst, Receptor Biol Lab, DK-2820 Gentofte, Denmark
关键词
D O I
10.1038/nrd917
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Type 2 diabetes mellitus - in which the body produces insufficient amounts of insulin or the insulin that is produced does not function properly to control blood glucose - is an increasingly common disorder. Prospective clinical studies have proven the benefits of tighter glucose control in reducing the frequency and severity of complications of the disease, leading to the advocation of earlier and more aggressive use of insulin therapy. Given the reluctance of patients with type 2 diabetes to inject themselves with insulin, orally active insulin mimetics would be a major therapeutic advance. Here, we discuss recent progress in understanding the structure-function relationships of the insulin and insulin-like growth factor 1 (IGF1) receptors, their mechanism of activation and their implications for the design of insulin-receptor agonists for diabetes therapy and IGF1-receptor antagonists for cancer therapy.
引用
收藏
页码:769 / 783
页数:15
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共 153 条
  • [101] Peptides identify the critical hotspots involved in the biological activation of the insulin receptor
    Pillutla, RC
    Hsiao, KC
    Beasley, JR
    Brandt, J
    Ostergaard, S
    Hansen, PH
    Spetzler, JC
    Danielsen, GM
    Andersen, AS
    Brissette, RE
    Lennick, M
    Fletcher, PW
    Blume, AJ
    Schäffer, L
    Goldstein, NI
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (25) : 22590 - 22594
  • [102] PULLEN RA, 1976, NATURE, V259, P369, DOI 10.1038/259369a0
  • [103] Mimicry of erythropoietin by a nonpeptide molecule
    Qureshi, SA
    Kim, RM
    Konteatis, Z
    Biazzo, DE
    Motamedi, H
    Rodrigues, R
    Boice, JA
    Calaycay, JR
    Bednarek, MA
    Griffin, P
    Gao, YD
    Chapman, K
    Mark, DF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (21) : 12156 - 12161
  • [104] RAFF M, 1979, PHYSICAL CHEM ASPECT, P116
  • [105] Tyrosine kinase inhibitors.: 14.: Structure-activity relationships for methylamino-substituted derivatives of 4-[(3-bromophenyl)amino]-6-(methylamino)pyrido[3,4-d]pyrimidine (PD 158780), a potent and specific inhibitor of the tyrosine kinase activity of receptors for the EGF family of growth factors
    Rewcastle, GW
    Murray, DK
    Elliott, WL
    Fry, DW
    Howard, CT
    Nelson, JM
    Roberts, BJ
    Vincent, PW
    Showalter, HDH
    Winters, RT
    Denny, WA
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (05) : 742 - 751
  • [106] A NOVEL HUMAN INSULIN-RECEPTOR GENE MUTATION UNIQUELY INHIBITS INSULIN BINDING WITHOUT IMPAIRING POSTTRANSLATIONAL PROCESSING
    ROACH, P
    ZICK, Y
    FORMISANO, P
    ACCILI, D
    TAYLOR, SI
    GORDEN, P
    [J]. DIABETES, 1994, 43 (09) : 1096 - 1102
  • [107] Congenital insulin resistance associated with a conformational alteration in a conserved β-sheet in the insulin receptor L1 domain
    Rouard, M
    Bass, J
    Grigorescu, F
    Garrett, TPJ
    Ward, CW
    Lipkind, G
    Jaffiole, C
    Steiner, DF
    Bell, GI
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) : 18487 - 18491
  • [108] New perspectives into the molecular pathogenesis and treatment of Type 2 diabetes
    Saltiel, AR
    [J]. CELL, 2001, 104 (04) : 517 - 529
  • [109] SCHAEFER EM, 1992, J BIOL CHEM, V267, P23393
  • [110] A MODEL FOR INSULIN BINDING TO THE INSULIN-RECEPTOR
    SCHAFFER, L
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 221 (03): : 1127 - 1132