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细胞通透性纳米抗体允许在未转染的活细胞中进行双色超分辨率显微镜观察。

Cell-Permeable Nanobodies Allow Dual-Color Super-Resolution Microscopy in Untransfected Living Cells.

机构信息

Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125, Berlin, Germany.

Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustrasse 3, 14189, Berlin, Germany.

出版信息

Angew Chem Int Ed Engl. 2021 Sep 27;60(40):22075-22080. doi: 10.1002/anie.202103068. Epub 2021 Aug 27.

Abstract

Super-resolution microscopy in living cells can be restricted by the availability of small molecule probes, which only exist against few targets and genetically encoded tags. Here, we expand the applicability of live-cell STED by engineering cell-permeable and highly fluorescent nanobodies as intracellular targeting agents. To ensure bright fluorescent signals at low concentrations we used the concept of intramolecular photostabilization by ligating a fluorophore along with the photostabilizer trolox to the nanobody using expressed protein ligation (EPL). Furthermore, these semi-synthetic nanobodies are equipped with a cleavable cell-penetrating peptide for efficient cellular entry, which enables super-resolution imaging of GFP and mCherry, as well as two endogenous targets, nuclear lamins and the DNA replication and repair protein PCNA. We monitored cell division and DNA replication via confocal and STED microscopy thus demonstrating the utility of these new intracellular tools for functional analysis.

摘要

活细胞中的超分辨率显微镜可能会受到小分子探针可用性的限制,这些探针仅针对少数目标和遗传编码标签存在。在这里,我们通过工程细胞渗透性和高荧光纳米体作为细胞内靶向剂来扩展活细胞 STED 的适用性。为了确保在低浓度下具有明亮的荧光信号,我们使用了通过将荧光团与光稳定剂trolox 一起连接到纳米体来实现分子内光稳定化的概念,使用表达蛋白连接 (EPL)。此外,这些半合成纳米体配备了可切割的穿透细胞膜肽,用于有效进入细胞,从而能够对 GFP 和 mCherry 以及两个内源性靶标核纤层和 DNA 复制和修复蛋白 PCNA 进行超分辨率成像。我们通过共聚焦和 STED 显微镜监测细胞分裂和 DNA 复制,从而证明了这些新的细胞内工具在功能分析中的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2472/8518916/b19cbed08024/ANIE-60-22075-g004.jpg

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