Dambacher Corey M, Lander Gabriel C
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA, USA.
Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA, USA.
J Struct Biol. 2015 Nov;192(2):151-8. doi: 10.1016/j.jsb.2015.09.010. Epub 2015 Sep 25.
Electron microscopy is commonly employed to determine the subunit organization of large macromolecular assemblies. However, the field lacks a robust molecular labeling methodology for unambiguous identification of constituent subunits. We present a strategy that exploits the unique properties of an unnatural amino acid in order to enable site-specific attachment of a single, readily identifiable protein label at any solvent-exposed position on the macromolecular surface. Using this method, we show clear labeling of a subunit within the 26S proteasome lid subcomplex that has not been amenable to labeling by traditional approaches.
电子显微镜常用于确定大型大分子组装体的亚基组织。然而,该领域缺乏一种强大的分子标记方法来明确识别组成亚基。我们提出了一种策略,利用非天然氨基酸的独特性质,以便在大分子表面任何溶剂暴露位置进行单一、易于识别的蛋白质标签的位点特异性连接。使用这种方法,我们在26S蛋白酶体盖子亚复合物中的一个亚基上实现了清晰的标记,而传统方法无法对该亚基进行标记。