Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, Massachusetts 02215, United States.
Université Côte d'Azur, CNRS, INSERM, IRCAN, 06100 Nice, France.
Bioconjug Chem. 2021 Nov 17;32(11):2397-2406. doi: 10.1021/acs.bioconjchem.1c00442. Epub 2021 Nov 8.
Site-specific protein labeling is important in biomedical research and biotechnology. While many methods allow site-specific protein modification, a straightforward approach for efficient N-terminal protein labeling is not available. We introduce a novel sortase-mediated swapping approach for a one-step site-specific N-terminal labeling with a near-quantitative yield. We show that this method allows rapid and efficient cleavage and simultaneous labeling of the N or C termini of fusion proteins. The method does not require any prior modification beyond the genetic incorporation of the sortase recognition motif. This new approach provides flexibility for protein engineering and site-specific protein modifications.
定点蛋白质标记在生物医学研究和生物技术中非常重要。虽然有许多方法可以实现定点蛋白质修饰,但目前还没有一种简单直接的方法能够高效地进行 N 端蛋白质标记。我们引入了一种新型的转肽酶介导的交换方法,可一步实现定点 N 端标记,收率接近定量。我们证明,该方法可以快速有效地切割和同时标记融合蛋白的 N 或 C 末端。该方法除了在遗传上引入转肽酶识别模体外,不需要任何预先修饰。这种新方法为蛋白质工程和定点蛋白质修饰提供了灵活性。