| Literature DB >> 28840953 |
Cheng Cui1, Hui Zhang1,2, Ruowen Wang1,3, Sena Cansiz1, Xiaoshu Pan1, Shuo Wan1, Weijia Hou1, Long Li1, Meiwan Chen4, Yuan Liu1,3, Xigao Chen1, Qiaoling Liu3, Weihong Tan1,3.
Abstract
Site-selective protein modification is a key step in facilitating protein functionalization and manipulation. To accomplish this, genetically engineered proteins were previously required, but the procedure was laborious, complex, and technically challenging. Herein we report the development of aptamer-based recognition-then-reaction to guide site-selective protein/DNA conjugation in a single step with outstanding selectivity and efficiency. As models, several proteins, including human thrombin, PDGF-BB, Avidin, and His-tagged recombinant protein, were studied, and the results showed excellent selectivity under mild reaction conditions. Taking advantage of aptamers as recognition elements with extraordinary selectivity and affinity, this simple preparation method can tag a protein in a complex milieu. Thus, with the aptamer obtained from cell-SELEX, real-time modification of live-cell membrane proteins can be achieved in one step without any pre-treatment.Entities:
Keywords: aptamer template; cell-surface modification; protein conjugation; site-selective
Mesh:
Substances:
Year: 2017 PMID: 28840953 PMCID: PMC5912682 DOI: 10.1002/anie.201706285
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336