Mechanisms in Cell Biology and Disease Research Group, School of Pharmacy and Medical Sciences, University of South Australia Cancer Research Institute, University of South Australia, Adelaide, SA 5000, Australia.
Adelaide Medical School and Freemasons Foundation Centre for Men's Health, University of Adelaide, Adelaide, SA 5000, Australia.
Int J Mol Sci. 2019 Nov 29;20(23):6035. doi: 10.3390/ijms20236035.
Syntenin-1 is an essential multi-functional adaptor protein, which has multiple roles in membrane trafficking and exosome biogenesis, as well as scaffolding interactions with either the actin cytoskeleton or focal adhesions. However, how this functional multiplicity relates to syntenin-1 distribution in different endosome compartments or other intracellular locations and its underlying involvement in cancer pathogenesis have yet to be fully defined. To help facilitate the investigation of syntenin-1 biology, we developed two specific monoclonal antibodies (Synt-2C6 and Synt-3A11) to spatially distinct linear sequence epitopes on syntenin-1, which were each designed to be unique at the six-amino acid level. These antibodies produced very different intracellular staining patterns, with Synt-2C6 detecting endosomes and Synt-3A11 producing a fibrillar staining pattern suggesting a cytoskeletal localisation. Treatment of cells with Nocodazole altered the intracellular localisation of Synt-3A11, which was consistent with the syntenin-1 protein interacting with microtubules. In prostate tissue biopsies, Synt-3A11 defined atrophy and early-stage prostate cancer, whereas Synt-2C6 only showed minimal interaction with atrophic tissue. This highlights a critical need for site-specific antibodies and a knowledge of their reactivity to define differential protein distributions, interactions and functions, which may differ between normal and malignant cells.
衔接蛋白-1 是一种必不可少的多功能衔接蛋白,它在膜运输和外体生物发生中具有多种作用,并且与肌动蛋白细胞骨架或焦点粘连具有支架相互作用。然而,这种多功能性与衔接蛋白-1 在不同内体隔室或其他细胞内位置的分布以及其在癌症发病机制中的潜在作用尚未完全确定。为了帮助促进衔接蛋白-1 生物学的研究,我们开发了两种针对衔接蛋白-1 上空间上不同的线性序列表位的特异性单克隆抗体(Synt-2C6 和 Synt-3A11),每个抗体都是在六个氨基酸水平上设计的独特抗体。这些抗体产生了非常不同的细胞内染色模式,Synt-2C6 检测到内体,而 Synt-3A11 产生纤维状染色模式,表明其定位于细胞骨架。用诺考达唑处理细胞会改变 Synt-3A11 的细胞内定位,这与衔接蛋白-1 蛋白与微管相互作用一致。在前列腺组织活检中,Synt-3A11 定义了萎缩和早期前列腺癌,而 Synt-2C6 仅与萎缩组织有最小的相互作用。这突出表明需要特定部位的抗体以及对其反应性的了解,以确定正常和恶性细胞之间可能存在差异的差异蛋白分布、相互作用和功能。