4.7 Article

An encoded viral micropatch for multiplex cellbased assays through localized gene delivery

Journal

LAB ON A CHIP
Volume 17, Issue 14, Pages 2435-2442

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7lc00372b

Keywords

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Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2012-0009555, 2012M3A7A9671610, 2015K1A4A3047345]
  2. Industrial Technology Innovation Program -Ministry of Trade, Industry & Energy (MI, Korea) [10050991]
  3. Kyung Hee University [KHU-20150514]
  4. Korea Evaluation Institute of Industrial Technology (KEIT) [10050991] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2012M3A7A9671610] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The increasing number of potential drug targets and compounds has led to the development of highthroughput cell-based assays. Simultaneous processing of multiple targets in the same experiment based on localized target gene expression is a very efficient strategy for this purpose. To address this need, we present an adenoviral vector-immobilized microparticle with two-dimensional (2D) shape-encoding properties that allows localized patch-like gene delivery to monolayer-cultured cells. This format conveniently achieves multiplexed gene delivery compatible with both high-throughput cellular assays and fluorescence high-content imaging instruments. A multiplex G protein-coupled receptor (GPCR) internalization assay was developed to demonstrate the compatibility of this system with high-throughput image-based cellular assays.

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