Understanding cytokine and growth factor receptor activation mechanisms

被引:68
作者
Atanasova, Mariya [1 ]
Whitty, Adrian [1 ]
机构
[1] Boston Univ, Dept Chem, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
Agonist antibodies; bell-shaped dose-response; erythropoietin receptor; ligand-induced dimerization; ligand-induced oligomerization; receptor pre-association; receptor-ligand cross-reactivity; small molecule receptor agonists; COLONY-STIMULATING FACTOR; HUMAN PROLACTIN RECEPTOR; AGONIST MONOCLONAL-ANTIBODIES; ERYTHROPOIETIN EPO RECEPTOR; RESONANCE ENERGY-TRANSFER; TYROSINE KINASE-ACTIVITY; LOW-AFFINITY INTERACTION; TRANSMEMBRANE DOMAIN; EGF RECEPTOR; HORMONE RECEPTOR;
D O I
10.3109/10409238.2012.729561
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
Our understanding of the detailed mechanism of action of cytokine and growth factor receptors - and particularly our quantitative understanding of the link between structure, mechanism and function - lags significantly behind our knowledge of comparable functional protein classes such as enzymes, G protein-coupled receptors, and ion channels. In particular, it remains controversial whether such receptors are activated by a mechanism of ligand-induced oligomerization, versus a mechanism in which the ligand binds to a pre-associated receptor dimer or oligomer that becomes activated through subsequent conformational rearrangement. A major limitation to progress has been the relative paucity of methods for performing quantitative mechanistic experiments on unmodified receptors expressed at endogenous levels on live cells. In this article, we review the current state of knowledge on the activation mechanisms of cytokine and growth factor receptors, critically evaluate the evidence for and against the different proposed mechanisms, and highlight other key questions that remain unanswered. New approaches and techniques have led to rapid recent progress in this area, and the field is poised for major advances in the coming years which promise to revolutionize our understanding of this large and biologically and medically important class of receptors.
引用
收藏
页码:502 / 530
页数:29
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共 219 条
  • [1] An extra high dose of erythropoietin fails to support the proliferation of erythropoietin dependent cell lines
    Abe, Satoshi
    Sasaki, Ryuzo
    Masuda, Seiji
    [J]. CYTOTECHNOLOGY, 2011, 63 (02) : 101 - 109
  • [2] Differential activation of cysteine-substitution mutants of fibroblast growth factor receptor 3 is determined by cysteine localization
    Adar, R
    Monsonego-Ornan, E
    David, P
    Yayon, A
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (05) : 860 - 868
  • [3] GDNF family neurotrophic factor signaling: Four masters, one servant?
    Airaksinen, MS
    Titievsky, A
    Saarma, M
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 1999, 13 (05) : 313 - 325
  • [4] The GDNF family: Signalling, biological functions and therapeutic value
    Airaksinen, MS
    Saarma, M
    [J]. NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) : 383 - 394
  • [5] Structural Basis for Negative Cooperativity in Growth Factor Binding to an EGF Receptor
    Alvarado, Diego
    Klein, Daryl E.
    Lemmon, Mark A.
    [J]. CELL, 2010, 142 (04) : 568 - 579
  • [6] Common γ chain cytokines:: Dissidence in the details
    Alves, Nuno L.
    Arosa, Fernando A.
    van Lier, Rene A. W.
    [J]. IMMUNOLOGY LETTERS, 2007, 108 (02) : 113 - 120
  • [7] Characterization of a soluble ternary complex formed between human interferon-β-1a and its receptor chains
    Arduini, RM
    Strauch, KL
    Runkel, LA
    Carlson, MM
    Hronowski, XP
    Foley, SF
    Young, CN
    Cheng, WJ
    Hochman, PS
    Baker, DP
    [J]. PROTEIN SCIENCE, 1999, 8 (09) : 1867 - 1877
  • [8] Transmembrane domain of EphA1 receptor forms dimers in membrane-like environment
    Artemenko, Elena O.
    Egorova, Natalya S.
    Arseniev, Alexander S.
    Feofanov, Alexey V.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2008, 1778 (10): : 2361 - 2367
  • [9] Will any dimer do?
    Ballinger, MD
    Wells, JA
    [J]. NATURE STRUCTURAL BIOLOGY, 1998, 5 (11) : 938 - 940
  • [10] CRYSTAL-STRUCTURE OF THE SOLUBLE HUMAN 55 KD TNF RECEPTOR-HUMAN TNF-BETA COMPLEX - IMPLICATIONS FOR TNF RECEPTOR ACTIVATION
    BANNER, DW
    DARCY, A
    JANES, W
    GENTZ, R
    SCHOENFELD, HJ
    BROGER, C
    LOETSCHER, H
    LESSLAUER, W
    [J]. CELL, 1993, 73 (03) : 431 - 445