Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE, USA.
Yeast. 2012 Mar;29(3-4):119-36. doi: 10.1002/yea.2895. Epub 2012 Apr 4.
During the past decade, it has become clear that protein function and regulation are highly dependent upon intracellular localization. Although fluorescent protein variants are ubiquitously used to monitor protein dynamics, localization and abundance; fluorescent light microscopy techniques often lack the resolution to explore protein heterogeneity and cellular ultrastructure. Several approaches have been developed to identify, characterize and monitor the spatial localization of proteins and complexes at the suborganelle level, yet many of these techniques have not been applied to yeast. Thus, we have constructed a series of cassettes containing codon-optimized epitope tags, fluorescent protein variants that cover the full spectrum of visible light, a TetCys motif used for fluorescein arsenical hairpin (FlAsH)-based localization, and the first evaluation in yeast of a photoswitchable variant, mEos2, to monitor discrete subpopulations of proteins via confocal microscopy. This series of modules, complete with six different selection markers, provides the optimal flexibility during live-cell imaging and multicolour labelling in vivo. Furthermore, high-resolution imaging techniques include the yeast-enhanced TetCys motif, which is compatible with diaminobenzidine photo-oxidation used for protein localization by electron microscopy, and mEos2, which is ideal for super-resolution microscopy. We have examined the utility of our cassettes by analysing all probes fused to the C-terminus of Sec61, a polytopic membrane protein of the endoplasmic reticulum of moderate protein concentration, in order to directly compare fluorescent probes, their utility and technical applications. Our series of cassettes expand the repertoire of molecular tools available to advance targeted spatiotemporal investigations using multiple live-cell, super-resolution or electron microscopy imaging techniques.
在过去的十年中,很明显蛋白质的功能和调节高度依赖于细胞内定位。尽管荧光蛋白变体被广泛用于监测蛋白质的动态、定位和丰度;荧光显微镜技术往往缺乏分辨率来探索蛋白质异质性和细胞超微结构。已经开发了几种方法来识别、表征和监测亚细胞器水平的蛋白质和复合物的空间定位,但这些技术中的许多尚未应用于酵母。因此,我们构建了一系列包含密码子优化的表位标签、涵盖可见光全谱的荧光蛋白变体、用于荧光素砷发夹(FlAsH)定位的 TetCys 基序,以及第一个在酵母中评估的光开关变体 mEos2,通过共聚焦显微镜监测蛋白质的离散亚群。该系列模块包含六种不同的选择标记,为活细胞成像和体内多色标记提供了最佳的灵活性。此外,高分辨率成像技术包括酵母增强的 TetCys 基序,该基序与二氨基联苯醌光氧化兼容,用于电子显微镜下的蛋白质定位,以及 mEos2,非常适合超分辨率显微镜。我们通过分析融合到内质网膜多跨膜蛋白 Sec61 C 末端的所有探针来检查我们的盒的实用性,以直接比较荧光探针、它们的实用性和技术应用。我们的一系列盒扩展了分子工具的范围,可用于使用多种活细胞、超分辨率或电子显微镜成像技术进行靶向时空研究。