Bernards Andre, Settleman Jeffrey
MGH Cancer Center and Harvard Medical School, 149 13th Street, Charlestown, MA 02129, USA.
Trends Cell Biol. 2004 Jul;14(7):377-85. doi: 10.1016/j.tcb.2004.05.003.
The small GTPases of the Ras superfamily mediate numerous biological processes through their ability to cycle between an inactive GDP-bound and an active GTP-bound form. Among the key regulators of GTPase cycling are the GTPase-activating proteins (GAPs), which stimulate the weak intrinsic GTP-hydrolysis activity of the GTPases, thereby inactivating them. Despite the abundance of GAPs and the fact that mutations in GAP-encoding genes underlie several human diseases, these proteins have received relatively little attention. Recent studies have addressed the regulatory mechanisms that influence GAP activity. So far, findings suggest that GAP activity is regulated by several mechanisms, including protein-protein interactions, phospholipid interactions, phosphorylation, subcellular translocation and proteolytic degradation.
Ras超家族的小GTP酶通过在无活性的GDP结合形式和活性的GTP结合形式之间循环的能力,介导众多生物学过程。GTP酶激活蛋白(GAPs)是GTP酶循环的关键调节因子之一,它刺激GTP酶微弱的内在GTP水解活性,从而使其失活。尽管GAPs数量众多,且编码GAP的基因突变是几种人类疾病的基础,但这些蛋白质受到的关注相对较少。最近的研究探讨了影响GAP活性的调控机制。到目前为止,研究结果表明,GAP活性受多种机制调控,包括蛋白质-蛋白质相互作用、磷脂相互作用、磷酸化、亚细胞易位和蛋白水解降解。