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INTEGRATED MICROFLUIDIC SELEX USING FREE SOLUTION ELECTROKINETICS.
Olsen, Timothy R; Tapia-Alveal, Claudia; Yang, Kyung-Ae; Zhang, Xin; Pereira, Leonardo Joe; Farmakidis, Nickolaos; Pei, Renjun; Stojanovic, Milan N; Lin, Qiao.
Afiliação
  • Olsen TR; Department of Mechanical Engineering, Columbia University, New York, NY, USA.
  • Tapia-Alveal C; Department of Medicine, Columbia University, New York, NY, USA.
  • Yang KA; Department of Medicine, Columbia University, New York, NY, USA.
  • Zhang X; Department of Mechanical Engineering, Columbia University, New York, NY, USA.
  • Pereira LJ; Department of Mechanical Engineering, Columbia University, New York, NY, USA.
  • Farmakidis N; Department of Mechanical Engineering, Columbia University, New York, NY, USA.
  • Pei R; Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, China.
  • Stojanovic MN; Department of Medicine, Columbia University, New York, NY, USA.
  • Lin Q; Department of Mechanical Engineering, Columbia University, New York, NY, USA.
J Electrochem Soc ; 164(5): B3122-B3129, 2017.
Article em En | MEDLINE | ID: mdl-29170564
ABSTRACT
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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article