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Combined Use of Unnatural Amino Acids Enables Dual-Color Super-Resolution Imaging of Proteins via Click Chemistry

机译:联合使用非天然氨基酸可以通过点击化学来实现蛋白质的双色超分辨率成像

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摘要

Recent advances in optical nanoscopy have brought the imaging resolution to the size of the individual macromolecules, thereby setting stringent requirements for the fluorescent labels. Such requirements are optimally fulfilled by the incorporation of unnatural amino acids (UAAs) in the proteins of interest (POIs), followed by fluorophore conjugation via click chemistry. However, this approach has been limited to single POIs in mammalian cells. Here we solve this problem by incorporating different UAAs in different POIs, which are expressed in independent cell sets. The cells are then fused, thereby combining the different proteins and organelles, and are easily imaged by dual-color super-resolution microscopy. This procedure, which we termed Fuse2Click, is simple, requires only the well-established Amber codon, and allows the use of all previously optimized UAAs and tRNA/RS pairs. This should render it a tool of choice for multicolor click-based imaging.
机译:光学纳米镜的最近进步使得成像分辨率使成像分辨率与单个大分子的大小,从而为荧光标记设定严格的要求。 通过在感兴趣的蛋白质(POI)中的不自然氨基酸(UAAs)掺入,然后通过点击化学来最佳地实现这些要求。 然而,这种方法仅限于哺乳动物细胞中的单痘。 在这里,我们通过在不同的POI中结合不同的uAA来解决这个问题,这些问题在独立的小区集中表示。 然后将细胞融合,从而组合不同的蛋白质和细胞器,并且通过双色超分辨率显微镜容易地成像。 我们称之为Fuse2Click的此过程很简单,只需要良好的琥珀色密码子,并允许使用所有先前优化的UAAS和TRNA / RS对。 这应该使其成为基于多色鼠标的成像的选择工具。

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