An Integrated Microfluidic SELEX Approach Using Combined Electrokinetic and Hydrodynamic Manipulation

被引:13
|
作者
Olsen, Timothy [1 ]
Zhu, Jing [1 ]
Kim, Jinho [1 ]
Pei, Renjun [2 ]
Stojanovic, Milan N. [3 ]
Lin, Qiao [1 ]
机构
[1] Columbia Univ, Dept Mech Engn, 220 SW Mudd,500 West 120th St, New York, NY 10027 USA
[2] Chinese Acad Sci, Suzhou Inst Nanotech & Nanobion, Suzhou, Peoples R China
[3] Columbia Univ, Dept Med, New York, NY USA
来源
SLAS TECHNOLOGY | 2017年 / 22卷 / 01期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
microfluidics; lab-on-a-chip; molecular biology; systems; IN-VITRO SELECTION; CANCER-CELLS; MICROMAGNETIC SELECTION; CLINICAL-APPLICATIONS; EMERGING CLASS; RNA MOLECULES; DNA APTAMERS; LIGANDS; BINDING; AFFINITY;
D O I
10.1177/2211068216659255
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This article presents a microfluidic approach for the integration of the process of aptamer selection via systematic evolution of ligands by exponential enrichment (SELEX). The approach employs bead-based biochemical reactions in which affinity-selected target-binding oligonucleotides are electrokinetically transferred for amplification, while the amplification product is transferred back for affinity selection via pressure-driven fluid flow. The hybrid approach simplifies the device design and operation procedures by reduced pressure-driven flow control requirements and avoids the potentially deleterious exposure of targets to electric fields prior to and during affinity selection. In addition, bead-based reactions are used to achieve the on-chip coupling of affinity selection and amplification of target-binding oligonucleotides, thereby realizing on-chip loop closure and integration of the entire SELEX process without requiring offline procedures. The microfluidic approach is thus capable of closed-loop, multiround aptamer enrichment as demonstrated by selection of DNA aptamers against the protein immunoglobulin E with high affinity (K-D = 12 nM) in a rapid manner (4 rounds in approximately 10 h).
引用
收藏
页码:63 / 72
页数:10
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