轨道轨道
质谱法
化学
吞吐量
共价键
克拉斯
色谱法
高通量筛选
组合化学
计算机科学
生物化学
有机化学
突变
基因
电信
无线
作者
Marcin Dyba,John-Paul Denson,Anna Maciąg
出处
期刊:Methods in molecular biology
日期:2024-01-01
卷期号:: 145-157
标识
DOI:10.1007/978-1-0716-3822-4_11
摘要
MALDI-TOF mass spectrometry enables high-throughput screening of covalent fragment libraries and SAR compound progressions of selective KRAS G12C inhibitors. Using the MALDI-TOF platform instead of the more traditional ESI-MS TOF/orbitrap instrumentation can radically shorten sample acquisition time, allowing up to 384 samples to be screened in 30 min. The typical throughput for a covalent library screen is 1152 samples per 8 h, including processing, calculation, and reporting steps. The throughput can be doubled without any significant assay modification.
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