Gao Feng, Gao Tang, Zhou Kechao, Zeng Wenbin
Powder Metallurgy Research Institute of Central South University, Changsha 410013, China.
The Third Xiangya Hospital, Central South University, Changsha 410013, China.
Molecules. 2016 Aug 31;21(9):1163. doi: 10.3390/molecules21091163.
Characterization of the chemical environment, movement, trafficking and interactions of proteins in live cells is essential to understanding their functions. Labeling protein with functional molecules is a widely used approach in protein research to elucidate the protein location and functions both in vitro and in live cells or in vivo. A peptide or a protein tag fused to the protein of interest and provides the opportunities for an attachment of small molecule probes or other fluorophore to image the dynamics of protein localization. Here we reviewed the recent development of no-wash small molecular probes for photoactive yellow protein (PYP-tag), by the means of utilizing a quenching mechanism based on the intramolecular interactions, or an environmental-sensitive fluorophore. Several fluorogenic probes have been developed, with fast labeling kinetics and cell permeability. This technology allows quick live-cell imaging of cell-surface and intracellular proteins without a wash-out procedure.
表征活细胞中蛋白质的化学环境、运动、运输和相互作用对于理解其功能至关重要。用功能分子标记蛋白质是蛋白质研究中广泛使用的一种方法,用于阐明蛋白质在体外、活细胞或体内的定位和功能。与目标蛋白融合的肽或蛋白质标签为附着小分子探针或其他荧光团以成像蛋白质定位动态提供了机会。在此,我们综述了用于光活性黄色蛋白(PYP标签)的免洗小分子探针的最新进展,其方法是利用基于分子内相互作用的淬灭机制或环境敏感荧光团。已经开发了几种荧光探针,具有快速标记动力学和细胞渗透性。该技术允许对细胞表面和细胞内蛋白质进行快速活细胞成像,而无需洗脱程序。