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

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

Small (Weinheim an der Bergstrasse, Germany) (2020-01-28)
Marius Brehm, Stefan Heissler, Sergii Afonin, Pavel A Levkin
要旨

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.

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製品内容

Sigma-Aldrich
ジメタクリル酸エチレングリコール, 98%, contains 90-110 ppm monomethyl ether hydroquinone as inhibitor
Sigma-Aldrich
2,2-ジメトキシ-2-フェニルアセトフェノン, 99%
Sigma-Aldrich
Fmoc-Ala-OH, 95%
Sigma-Aldrich
tert-ブチルイソシアニド, 98%
Sigma-Aldrich
Fmoc-Leu-OH, ≥97.0%
Sigma-Aldrich
Fmoc-Val-OH, ≥98.0% (HPLC)
Sigma-Aldrich
シクロヘキシルイソシアニド, 98%
Sigma-Aldrich
N-Boc-2-アミノアセトアルデヒド, 95%
Sigma-Aldrich
2,4-ジヒドロキシベンゾフェノン, 99%
Sigma-Aldrich
イソシアン化ベンジル, 98%
Sigma-Aldrich
1-N-Boc-2-ピペリドン, 97%