Department of Biological Sciences and Institute for RNA Science and Technology, University at Albany, State University of New York, Albany, NY 12222, USA.
Nucleic Acids Res. 2010 Apr;38(7):e93. doi: 10.1093/nar/gkp1207. Epub 2010 Jan 6.
Induction of molecular proximity can mediate a discrete functional response in biological systems. Therefore, creating new and specific connectivity between non-interacting proteins is a means of imposing rational control over biological processes. According to this principle, here we use composite RNA aptamers to generate molecular adaptors that link various 'target' molecules to a common 'utility' molecule, with the utility molecule being an entry point to a pathway conscripted to process the target molecule. In particular, we created a bi-functional aptamer that simultaneously binds to the green fluorescent protein (serving as a surrogate extracellular target) and the opsonin C3b/iC3b (serving as the utility molecule). This bi-functional aptamer enabled us to commandeer the C3-based opsonization-phagocytosis pathway to selectively transport an extracellular target into the lysosome for degradation. This novel strategy has the potential for powerful therapeutic applications with extracellular proteins involved in tumor development or surface markers on cancer cells as the target molecules.
分子接近诱导可以介导生物系统中的离散功能反应。因此,在非相互作用的蛋白质之间创建新的和特定的连接是对生物过程进行理性控制的一种手段。根据这一原则,在这里,我们使用复合 RNA 适体来产生分子接头,将各种“靶”分子连接到一个共同的“实用”分子上,其中实用分子是进入途径的入口,该途径被征召来处理靶分子。具体来说,我们创建了一种双功能适体,它可以同时结合绿色荧光蛋白(作为替代细胞外靶标)和调理素 C3b/iC3b(作为实用分子)。这种双功能适体能使我们利用基于 C3 的调理作用-吞噬作用途径将细胞外靶标选择性地输送到溶酶体中进行降解。这种新策略有可能在外周蛋白参与肿瘤发展或癌细胞表面标志物作为靶标分子的情况下,具有强大的治疗应用潜力。