Igarashi Tomoko, Oishi Yuko, Araki Satohiko, Mori Hidezo, Takeda Soichi
Department of Cardiac Physiology, National Cardiovascular Center Research Institute, 5-7-1 Fujishiro-dai, Suita, Osaka 565-8565, Japan.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006 Jul 1;62(Pt 7):688-91. doi: 10.1107/S1744309106022548. Epub 2006 Jun 26.
VAPs are haemorrhagic snake-venom toxins belonging to the reprolysin family of zinc metalloproteinases. In vitro, VAPs induce apoptosis specifically in cultured vascular endothelial cells. VAPs have a modular structure that bears structural homology to mammalian ADAMs (a disintegrin and metalloproteinases). VAP1 is a homodimer with a MW of 110 kDa in which the monomers are connected by a single disulfide bridge. VAP2 is homologous to VAP1 and exists as a monomer with a MW of 55 kDa. In the current study, several crystal forms of VAP1 and VAP2 were obtained using the vapour-diffusion method and diffraction data sets were collected using SPring-8 beamlines. The best crystals of VAP1 and VAP2 generated data sets to 2.5 and 2.15 angstroms resolution, respectively.
血管凋亡蛋白(VAPs)是属于锌金属蛋白酶解整合素家族的出血性蛇毒毒素。在体外,VAPs可特异性诱导培养的血管内皮细胞凋亡。VAPs具有模块化结构,与哺乳动物的ADAMs(一种解整合素和金属蛋白酶)具有结构同源性。VAP1是一种分子量为110 kDa的同型二聚体,其中单体通过单个二硫键连接。VAP2与VAP1同源,以分子量为55 kDa的单体形式存在。在本研究中,采用气相扩散法获得了VAP1和VAP2的几种晶体形式,并使用SPring-8光束线收集了衍射数据集。VAP1和VAP2的最佳晶体分别产生了分辨率为2.5埃和2.15埃的数据集。