Sinclair Ian, Stearns Rick, Pringle Steven, Wingfield Jonathan, Datwani Sammy, Hall Eric, Ghislain Luke, Majlof Lars, Bachman Martin
SSCM AstraZeneca Alderley Park, Macclesfield, UK
Labcyte, Inc., Sunnyvale, CA, USA.
J Lab Autom. 2016 Feb;21(1):19-26. doi: 10.1177/2211068215619124. Epub 2015 Dec 2.
High-throughput, direct measurement of substrate-to-product conversion by label-free detection, without the need for engineered substrates or secondary assays, could be considered the "holy grail" of drug discovery screening. Mass spectrometry (MS) has the potential to be part of this ultimate screening solution, but is constrained by the limitations of existing MS sample introduction modes that cannot meet the throughput requirements of high-throughput screening (HTS). Here we report data from a prototype system (Echo-MS) that uses acoustic droplet ejection (ADE) to transfer femtoliter-scale droplets in a rapid, precise, and accurate fashion directly into the MS. The acoustic source can load samples into the MS from a microtiter plate at a rate of up to three samples per second. The resulting MS signal displays a very sharp attack profile and ions are detected within 50 ms of activation of the acoustic transducer. Additionally, we show that the system is capable of generating multiply charged ion species from simple peptides and large proteins. The combination of high speed and low sample volume has significant potential within not only drug discovery, but also other areas of the industry.
通过无标记检测对底物到产物的转化进行高通量直接测量,无需工程化底物或二次检测,这可被视为药物发现筛选的“圣杯”。质谱(MS)有潜力成为这一终极筛选解决方案的一部分,但受限于现有质谱样品引入模式的局限性,无法满足高通量筛选(HTS)的通量要求。在此,我们报告了一个原型系统(Echo-MS)的数据,该系统使用声滴喷射(ADE)以快速、精确和准确的方式将飞升规模的液滴直接转移到质谱仪中。声源可以以每秒高达三个样品的速率从微孔板将样品加载到质谱仪中。所得到的质谱信号显示出非常尖锐的起始轮廓,并且在声换能器激活后50毫秒内就能检测到离子。此外,我们表明该系统能够从简单肽和大蛋白质中产生多电荷离子物种。高速和低样品量的结合不仅在药物发现领域,而且在该行业的其他领域都具有巨大潜力。