An Integrated Microfluidic Processor for DNA-Encoded Combinatorial Library Functional Screening

被引:66
作者
MacConnell, Andrew B. [1 ,2 ]
Price, Alexander K. [1 ]
Paegel, Brian M. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, 130 Scripps Way, Jupiter, FL 33458 USA
[2] Scripps Res Inst, Doctoral Program Chem & Biol Sci, 130 Scripps Way, Jupiter, FL 33458 USA
关键词
DNA-encoded synthesis; combinatorial compound libraries; miniaturized automation; IONIZATION MASS-SPECTROMETRY; IN-VITRO SELECTION; ENZYME-INHIBITORS; DRUG DISCOVERY; DROPLETS; CELLS; BEAD; IDENTIFICATION; EXPRESSION; EVOLUTION;
D O I
10.1021/acscombsci.6b00192
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
DNA-encoded synthesis is rekindling interest in combinatorial compound libraries for drug discovery and in technology for automated and quantitative library screening. Here, we disclose a microfluidic circuit that enables functional screens of DNA-encoded compound beads. The device carries out library bead distribution into picoliter-scale assay reagent droplets, photochemical cleavage of compound from the bead, assay incubation, laser-induced fluorescence-based assay detection, and fluorescence-activated droplet sorting to isolate hits. DNA-encoded compound beads (10-mu m diameter) displaying a photocleavable positive control inhibitor pepstatin A were mixed (1920 beads, 729 encoding sequences) with negative control beads (58 000 beads, 1728 encoding sequences) and screened for cathepsin D inhibition using a biochemical enzyme activity assay. The circuit sorted 1518 hit droplets for collection following 18 min incubation over a 240 min analysis. Visual inspection of a subset of droplets (1188 droplets) yielded a 24% false discovery rate (1166 pepstatin A beads; 366 negative control beads). Using template barcoding strategies, it was possible to count hit collection beads (1863) using next-generation sequencing data. Bead-specific barcodes enabled replicate counting, and the false discovery rate was reduced to 2.6% by only considering hit-encoding sequences that were observed on >2 beads. This work represents a complete distributable small molecule discovery platform, from microfluidic miniaturized automation to ultrahigh-throughput hit deconvolution by sequencing.
引用
收藏
页码:181 / 192
页数:12
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