Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Cell Signal. 2017 Dec;40:133-142. doi: 10.1016/j.cellsig.2017.09.008. Epub 2017 Sep 18.
Vav1/2/3 comprise a protein family with guanyl nucleotide exchange activity for Rho and Rac as well as with motifs conferring adapter activity. Biologically, Vav1 plays a critical role in hematologic cell signaling, whereas Vav2/3 have a wider tissue distribution, but all 3 Vav proteins are implicated in cancer development. A structural feature of Vav1/2/3 is the presence of an atypical C1 domain, which possesses close structural homology to the typical C1 domains of protein kinase C but which fails to bind the second messenger diacylglycerol or the potent analogs, the phorbol esters. Previously, we have shown that five residues in the Vav1 C1 domain are responsible for its lack of phorbol ester binding. Here, we show that the lack of phorbol ester binding of Vav3 has a similar basis. We then explore the consequences of phorbol ester binding to a modified Vav3 in which the C1 domain has been altered to allow phorbol ester binding. We find both disruption of the guanyl nucleotide exchange activity of the modified Vav 3 as well as a shift in localization to the membrane upon phorbol ester treatment. This change in localization is associated with altered interactions with other signaling proteins. The studies provide a first step in assessing the potential for the design of custom C1 domain targeted molecules selective for the atypical C1 domains of Vav family proteins.
Vav1/2/3 组成一个具有鸟嘌呤核苷酸交换活性的蛋白家族,可交换 Rho 和 Rac 的鸟嘌呤核苷酸,并且具有赋予衔接活性的基序。在生物学上,Vav1 在血液细胞信号转导中发挥关键作用,而 Vav2/3 具有更广泛的组织分布,但所有 3 种 Vav 蛋白都与癌症的发展有关。Vav1/2/3 的一个结构特征是存在非典型的 C1 结构域,该结构域与蛋白激酶 C 的典型 C1 结构域具有密切的结构同源性,但不能结合第二信使二酰基甘油或强效类似物佛波酯。以前,我们已经表明,Vav1 C1 结构域中的五个残基负责其缺乏佛波酯结合。在这里,我们表明 Vav3 缺乏佛波酯结合具有类似的基础。然后,我们探讨了修饰后的 Vav3 结合佛波酯的后果,其中 C1 结构域已被改变以允许佛波酯结合。我们发现,经过佛波酯处理后,修饰后的 Vav3 的鸟嘌呤核苷酸交换活性被破坏,并且定位向膜转移。这种定位的变化与与其他信号蛋白的相互作用的改变有关。这些研究为评估设计针对 Vav 家族蛋白的非典型 C1 结构域的定制 C1 结构域靶向分子的潜力提供了第一步。