High-Throughput Bioassays using "Dip-and-Go" Multiplexed Electrospray Mass Spectrometry

被引:23
|
作者
Wei, Zhenwei [1 ]
Xie, Zhuoer [1 ]
Kuvelkar, Reshma [2 ]
Shah, Vinit [2 ]
Bateman, Kevin [2 ]
McLaren, David G. [2 ]
Cooks, R. Graham [1 ]
机构
[1] Purdue Univ, Dept Chem, Aston Labs, 560 Oval Dr, W Lafayette, IN 47906 USA
[2] Merck & Co Inc, 2000 Galloping Hill Rd, Kenilworth, NJ 07033 USA
关键词
enzyme inhibition; field amplification; inductive nanoelectrospray; micro electrophoresis; pharmacokinetics; NANOELECTROSPRAY IONIZATION; DRUG DISCOVERY; SAMPLE; PERFORMANCE; ASSAY; IDENTIFICATION; INTERFACE; STACKING;
D O I
10.1002/anie.201909047
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A multiplexed system based on inductive nanoelectrospray mass spectrometry (nESI-MS) has been developed for high-throughput screening (HTS) bioassays. This system combines inductive nESI and field amplification micro-electrophoresis to achieve a "dip-and-go" sample loading and purification strategy that enables nESI-MS based HTS assays in 96-well microtiter plates. The combination of inductive nESI and micro-electrophoresis makes it possible to perform efficient in situ separations and clean-up of biological samples. The sensitivity of the system is such that quantitative analysis of peptides from 1-10000nm can be performed in a biological matrix. A prototype of the automation system has been developed to handle 12 samples (one row of a microtiter plate) at a time. The sample loading and electrophoretic clean-up of biosamples can be done in parallel within 20s followed by MS analysis at a rate of 1.3 to 3.5s per sample. The system was used successfully for the quantitative analysis of BACE1-catalyzed peptide hydrolysis, a prototypical HTS assay of relevance to drug discovery. IC50 values for this system were in agreement with LC-MS but recorded in times more than an order of magnitude shorter.
引用
收藏
页码:17594 / 17598
页数:5
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