Integrated Microfluidic Selex Using Free Solution Electrokinetics

被引:15
作者
Olsen, Timothy R. [1 ]
Tapia-Alveal, Claudia [2 ]
Yang, Kyung-Ae [2 ]
Zhang, Xin [1 ]
Pereira, Leonardo Joe [1 ]
Farmakidis, Nickolaos [1 ]
Pei, Renjun [3 ]
Stojanovic, Milan N. [2 ]
Lin, Qiao [1 ]
机构
[1] Columbia Univ, Dept Mech Engn, New York, NY 10027 USA
[2] Columbia Univ, Dept Med, New York, NY 10032 USA
[3] Chinese Acad Sci, Suzhou Inst Nanotech & Nanobion, Suzhou, Peoples R China
基金
美国国家卫生研究院;
关键词
IN-VITRO SELECTION; EMERGING CLASS; RNA MOLECULES; DNA APTAMERS; LIGANDS; BINDING; CELLS; CHIP; IDENTIFICATION; ARGININE;
D O I
10.1149/2.0191705jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Systematic evolution of ligands by exponential enrichment (SELEX) offers a powerful method to isolate affinity oligonucleotides known as aptamers, which can then be used in a wide range of applications from drug delivery to biosensing. However, conventional SELEX methods rely on labor intensive and time consuming benchtop operations. A simplified microfluidic approach is presented which allows integration of the affinity selection and amplification stages of SELEX for the isolation of target-binding oligonucleotides by combining bead-based biochemical reactions with free solution electrokinetic oligonucleotide transfer. Free solution electrokinetics allows coupling of affinity selection and amplification for closed loop oligonucleotide enrichment without the need for offline processes, flow handling components or gel components, while bead based selection and amplification allow efficient manipulation of reagents and reaction products thereby realizing on-chip loop closure and integration of the entire SELEX process. Thus the approach is capable of multi-round enrichment of oligonucleotides using simple transfer processes while maintaining a high level of device integration, as demonstrated by the isolation of an aptamer pool against a protein target (IgA) with significantly higher binding affinity than the starting library in approximately 4 hours of processing time. (C) The Author( s) 2017. Published by ECS.
引用
收藏
页码:B3122 / B3129
页数:8
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