Nanomolar Synthesis in Droplet Microarrays with UV-Triggered On-Chip Cell Screening

被引:28
作者
Brehm, Marius [1 ]
Heissler, Stefan [2 ]
Afonin, Sergii [3 ]
Levkin, Pavel A. [1 ,4 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Toxicol & Genet, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[2] Karlsruhe Inst Technol KIT, Inst Funct Interfaces, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol KIT, Inst Biol Interfaces IBG 2, POB 3640, D-76021 Karlsruhe, Germany
[4] Karlsruhe Inst Technol KIT, Inst Organ Chem, Fritz Haber Weg 6, D-76131 Karlsruhe, Germany
基金
欧洲研究理事会;
关键词
high throughput; nanomolar; photorelease; screening; solid-phase synthesis; PEPTIDE ARRAYS; SPOT SYNTHESIS; MULTICOMPONENT REACTIONS; COMBINATORIAL SYNTHESIS; DRUG DISCOVERY; PLATFORM;
D O I
10.1002/smll.201905971
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Miniaturization and parallelization of combinatorial organic synthesis is important to accelerate the process of drug discovery while reducing the consumption of reagents and solvents. This work presents a miniaturized platform for on-chip solid-phase combinatorial library synthesis with UV-triggered on-chip cell screening. The platform is based on a nanoporous polymer coating on a glass slide, which is modified via photolithography to yield arrays of hydrophilic (HL) spots surrounded by superhydrophobic (SH) surface. The combination of HL spots and SH background enables confinement of nanoliter droplets, functioning as miniaturized reactors for the solid-phase synthesis. The polymer serves as support for nanomolar solid-phase synthesis, while a photocleavable linker enables the release of the synthesized compounds into the droplets containing live cells. A 588 compound library of bisamides is synthesized via a four-component Ugi reaction on the chip and products are detected via stamping of the droplet array onto a conductive substrate and subsequent matrix-assisted laser desorption ionization mass spectrometry. The light-induced cleavage shows high flexibility in screening conditions by spatial, temporal, and quantitative control.
引用
收藏
页数:10
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