Science for Life Laboratory, Department of Medical Biochemistry and Biophysics, Division of Genome Biology, Karolinska Institutet, Stockholm, 17165, Sweden.
Ming Wai Lau Centre for Reparative Medicine, Stockholm node, Karolinska Institutet, Stockholm, 17165, Sweden.
J Am Chem Soc. 2020 Nov 25;142(47):20080-20087. doi: 10.1021/jacs.0c09574. Epub 2020 Nov 11.
Genetically encoded fluorescent tags for visualization of proteins in living cells add six to several hundred amino acids to the protein of interest. While suitable for most proteins, common tags easily match and exceed the size of microproteins of 60 amino acids or less. The added molecular weight and structure of such fluorescent tag may thus significantly affect biophysical and biochemical properties of microproteins. Here, we develop single-residue terminal labeling (STELLA) tags that introduce a single noncanonical amino acid either at the N- or C-terminus of a protein or microprotein of interest for subsequent specific fluorescent labeling. Efficient terminal noncanonical amino acid mutagenesis is achieved using a precursor tag that is tracelessly cleaved. Subsequent selective bioorthogonal reaction with a cell-permeable organic dye enables live cell imaging of microproteins with minimal perturbation of their native sequence. The use of terminal residues for labeling provides a universally applicable and easily scalable strategy, which avoids alteration of the core sequence of the microprotein.
用于活细胞中蛋白质可视化的基因编码荧光标签会给目标蛋白质添加六到几百个氨基酸。虽然适用于大多数蛋白质,但常见的标签很容易匹配并超过 60 个氨基酸的微蛋白的大小。因此,这种荧光标签的添加分子量和结构可能会显著影响微蛋白的生物物理和生化特性。在这里,我们开发了单残基末端标记 (STELLA) 标签,可以在目标蛋白质或微蛋白的 N 端或 C 端引入单个非天然氨基酸,以便随后进行特异性荧光标记。通过使用无痕迹切割的前体标签,可以实现高效的末端非天然氨基酸诱变。随后与细胞通透的有机染料进行选择性生物正交反应,可在最小干扰微蛋白天然序列的情况下对其进行活细胞成像。使用末端残基进行标记提供了一种普遍适用且易于扩展的策略,避免了微蛋白核心序列的改变。