质谱法
吞吐量
药物发现
分析物
高通量筛选
色谱法
纳米技术
小分子
化学
生物标志物发现
样品制备
蛋白质组学
计算机科学
生化工程
计算生物学
材料科学
生物
电信
无线
生物化学
基因
工程类
作者
Jon D. Williams,Fan Pu,James W. Sawicki,Nathaniel L. Elsen
标识
DOI:10.1080/17460441.2023.2293153
摘要
The fast analysis time provided by uHT-MS is transforming how biochemical and chemical assays are performed in drug discovery. The potential to associate phenotypic responses produced by 1000's of compound treatments with changes in endogenous metabolite and lipid signals is becoming feasible. With the augmentation of simple, fast, high-throughput sample preparation, the scope of uHT-MS usage will increase. However, it likely will not supplant LC-MS for analyses that require low detection limits from complex matrices or characterization of complex biotherapeutics such as antibody-drug conjugates.
科研通智能强力驱动
Strongly Powered by AbleSci AI