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通过共价适体对蛋白酪氨酸激酶 7 的细胞表面标记和检测。

Cell Surface Labeling and Detection of Protein Tyrosine Kinase 7 via Covalent Aptamers.

机构信息

Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.

出版信息

J Am Chem Soc. 2023 Aug 2;145(30):16458-16463. doi: 10.1021/jacs.3c02752. Epub 2023 Jul 20.

Abstract

Covalent aptamers are novel biochemical tools for fast and selective transfer of labels to target proteins. Equipped with cleavable electrophiles, these nucleic acid probes enable the installation of functional handles onto native proteins. The high affinity and specificity with which aptamers bind their selected targets allows for quick, covalent labeling that can compete with nuclease-mediated degradation. Here, we introduce the first application of covalent aptamers to modify a specific cell surface protein through proximity-driven label transfer. We targeted protein tyrosine kinase 7 (PTK7), a prominent cancer marker, and demonstrated aptamer-mediated biotin transfer to specific lysine residues on the extracellular domain of the protein. This allowed for tracking of PTK7 expression, localization, and cellular internalization. These studies validate the programmability of covalent aptamers and highlight their applicability in a cellular context, including protein and small molecule delivery.

摘要

共价适体是一种新颖的生化工具,可快速、选择性地将标记物转移到靶蛋白上。这些核酸探针配备可裂解的亲电试剂,可将功能接头安装到天然蛋白质上。适体与其选定靶标结合的高亲和力和特异性允许快速、共价标记,可与核酸酶介导的降解竞争。在这里,我们首次将共价适体应用于通过邻近驱动的标记转移来修饰特定的细胞表面蛋白。我们将目标对准蛋白酪氨酸激酶 7(PTK7),这是一种突出的癌症标志物,并证明适体介导的生物素转移到蛋白质胞外结构域上的特定赖氨酸残基上。这允许跟踪 PTK7 的表达、定位和细胞内化。这些研究验证了共价适体的可编程性,并强调了它们在细胞环境中的适用性,包括蛋白质和小分子的递药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10401710/d5521ecec08c/ja3c02752_0002.jpg

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