Ackerson Christopher J, Jadzinsky Pablo D, Jensen Grant J, Kornberg Roger D
Department of Structural Biology, Stanford University School of Medicine, California 94305, USA.
J Am Chem Soc. 2006 Mar 1;128(8):2635-40. doi: 10.1021/ja0555668.
A general method of rigid, specific labeling of proteins with gold clusters has been devised. The method relies on the conjugation of a glutathione monolayer-protected gold cluster (MPC) with a single chain Fv antibody fragment (scFv), mutated to present an exposed cysteine residue. Efficient formation of a gold-thiolate bond between the MPC and scFv depends on activation of the gold cluster by chemical oxidation. Once formed, the MPC-scFv conjugate is treated with a reductant to quench cluster reactivity. The procedure has been performed with an MPC with an average Au(71) core and an scFv directed against a tetrameric protein, the influenza neuraminidase. A complex of the MPC-scFv conjugate with the neuraminidase was isolated, and the presence of four gold clusters was verified by cryoelectron microscopy.
已经设计出一种用金簇对蛋白质进行刚性、特异性标记的通用方法。该方法依赖于将谷胱甘肽单层保护的金簇(MPC)与单链Fv抗体片段(scFv)缀合,scFv经过突变以呈现一个暴露的半胱氨酸残基。MPC和scFv之间高效形成金硫键取决于通过化学氧化对金簇的激活。一旦形成,MPC-scFv缀合物用还原剂处理以淬灭簇的反应活性。该程序已使用具有平均Au(71)核心的MPC和针对四聚体蛋白流感神经氨酸酶的scFv进行。分离出MPC-scFv缀合物与神经氨酸酶的复合物,并通过冷冻电子显微镜验证了四个金簇的存在。