| Literature DB >> 27601357 |
Liqin Zhang1,2, Zunyi Yang3, Thu Le Trinh4, I-Ting Teng1, Sai Wang1, Kevin M Bradley3, Shuichi Hoshika3, Qunfeng Wu4, Sena Cansiz1, Diane J Rowold3, Christopher McLendon3, Myong-Sang Kim3, Yuan Wu1,2, Cheng Cui1, Yuan Liu1, Weijia Hou1, Kimberly Stewart1, Shuo Wan1, Chen Liu5, Steven A Benner6, Weihong Tan7,8.
Abstract
Laboratory in vitro evolution (LIVE) might deliver DNA aptamers that bind proteins expressed on the surface of cells. In this work, we used cell engineering to place glypican 3 (GPC3), a possible marker for liver cancer theranostics, on the surface of a liver cell line. Libraries were then built from a six-letter genetic alphabet containing the standard nucleobases and two added nucleobases (2-amino-8H-imidazo[1,2-a][1,3,5]triazin-4-one and 6-amino-5-nitropyridin-2-one), Watson-Crick complements from an artificially expanded genetic information system (AEGIS). With counterselection against non-engineered cells, eight AEGIS-containing aptamers were recovered. Five bound selectively to GPC3-overexpressing cells. This selection-counterselection scheme had acceptable statistics, notwithstanding the possibility that cells engineered to overexpress GPC3 might also express different off-target proteins. This is the first example of such a combination.Entities:
Keywords: aptamers; artificial nucleobases; cell engineering; glypican 3; laboratory evolution
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Year: 2016 PMID: 27601357 PMCID: PMC5554412 DOI: 10.1002/anie.201605058
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336