DeGiorgis Joseph A, Petukhova Tatyana A, Evans Teresa A, Reese Thomas S
Laboratory of Neurobiology, NINDS, National Institutes of Health, Building 49, Room 3A60, 49 Convent Drive, Bethesda, MD 20892, USA.
Traffic. 2008 Nov;9(11):1867-77. doi: 10.1111/j.1600-0854.2008.00809.x. Epub 2008 Aug 4.
Conventional kinesin (Kinesin-1), the founding member of the kinesin family, was discovered in the squid giant axon, where it is thought to move organelles on microtubules. In this study, we identify a second squid kinesin by searching an expressed sequence tag database derived from the ganglia that give rise to the axon. The full-length open reading frame encodes a 1753 amino acid sequence that classifies this protein as a Kinesin-3. Immunoblots demonstrate that this kinesin, unlike Kinesin-1, is highly enriched in chaotropically stripped axoplasmic organelles, and immunogold electron microscopy (EM) demonstrates that Kinesin-3 is tightly bound to the surfaces of these organelles. Video microscopy shows that movements of purified organelles on microtubules are blocked, but organelles remain attached, in the presence Kinesin-3 antibody. Immunogold EM of axoplasmic spreads with antibody to Kinesin-3 decorates discrete sites on many, but not all, free organelles and localizes Kinesin-3 to organelle/microtubule interfaces. In contrast, label for Kinesin-1 decorates microtubules but not organelles. The presence of Kinesin-3 on purified organelles, the ability of an antibody to block their movements along microtubules, the tight association of Kinesin-3 with motile organelles and its distribution at the interface between native organelles and microtubules suggest that Kinesin-3 is a dominant motor in the axon for unidirectional movement of organelles along microtubules.
传统驱动蛋白(驱动蛋白-1)是驱动蛋白家族的首个成员,在枪乌贼巨大轴突中被发现,人们认为它在微管上移动细胞器。在本研究中,我们通过搜索源自产生轴突的神经节的表达序列标签数据库,鉴定出第二种枪乌贼驱动蛋白。全长开放阅读框编码一个1753个氨基酸的序列,该蛋白被归类为驱动蛋白-3。免疫印迹表明,与驱动蛋白-1不同,这种驱动蛋白在经离液剂处理去除膜的轴浆细胞器中高度富集,免疫金电子显微镜(EM)显示驱动蛋白-3紧密结合在这些细胞器表面。视频显微镜观察表明,在存在驱动蛋白-3抗体的情况下,纯化细胞器在微管上的移动受阻,但细胞器仍保持附着。用抗驱动蛋白-3抗体对轴浆铺片进行免疫金EM显示,许多(但不是全部)游离细胞器上的离散位点被标记,并且驱动蛋白-3定位于细胞器/微管界面。相比之下,驱动蛋白-1的标记物标记微管而非细胞器。纯化细胞器上存在驱动蛋白-3、抗体阻断其沿微管移动的能力、驱动蛋白-3与运动细胞器的紧密结合及其在天然细胞器和微管之间界面处的分布表明,驱动蛋白-3是轴突中细胞器沿微管单向移动的主要动力蛋白。