Molecular Enzymology Group, University of Groningen, Nijenborgh 4, Groningen 9747AG, The Netherlands.
Bioconjug Chem. 2021 Aug 18;32(8):1559-1563. doi: 10.1021/acs.bioconjchem.1c00306. Epub 2021 Jul 24.
Site-specific protein labeling methods are highly valuable tools for research and applications. We present a new protein labeling method that allows covalent attachment of a chromo- and fluorogenic flavin (FMN) to any targeted protein using a short flavinylation peptide-tag. We show that this peptide can be as short as 7 residues and can be located at the N-terminus, C-terminus, or in internal regions of the target protein. Analogous to kinase-catalyzed phosphorylation, the flavin is covalently attached via a stable phosphothreonyl linkage. The site-specific covalent tethering of FMN is accomplished by using a bacterial flavin transferase. The covalent coupling of FMN was shown to work in and cells and could be performed , rendering the "Flavin-tag" method a powerful tool for the selective decoration of proteins with a biocompatible redox-active fluorescent chromophore.
基于定位的蛋白质标记方法是极具研究和应用价值的工具。我们提出了一种新的蛋白质标记方法,它利用短的黄素化肽标签,实现了将发色团和荧光团黄素(FMN)共价连接到任何靶向蛋白质上。我们证明,该肽段最短可以只有 7 个残基,且可以位于靶蛋白的 N 端、C 端或内部区域。类似激酶催化的磷酸化,黄素通过稳定的磷酰基连接共价连接。FMN 的特异性共价连接是通过使用细菌黄素转移酶来完成的。实验证明 FMN 的共价偶联可在 和 细胞中进行,并且可以在 时进行,这使得“黄素标签”方法成为了一种强大的工具,可用于将生物相容性的氧化还原活性荧光发色团选择性地修饰蛋白质。