化学
分馏
色谱法
样品制备
单克隆抗体
消化(炼金术)
串联质谱法
液相色谱-质谱法
质谱法
抗体
免疫学
生物
作者
Delia Li,Adam Farchone,Qing Zhu,Frank Macchi,Donald E. Walker,David A. Michels,Feng Yang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2020-07-29
卷期号:92 (17): 11888-11894
被引量:16
标识
DOI:10.1021/acs.analchem.0c02258
摘要
Residual host cell proteins (HCPs) present in biotherapeutics can pose potential safety risks for patients or affect product stability, thus prompting a critical need to monitor HCPs in drug substance or product to ensure product safety and quality. Current approaches for robust HCP identification at or above 10 ppm levels require either concatenated peptide fractionation or enrichment via antibody depletion, which challenges the direct quantitation of HCPs. This paper describes a simple, fast sample preparation method without the need for sample fractionation or enrichment; instead, we utilize trypsin-friendly sodium deoxycholate (SDC) as an advantageous denaturant that can be effectively removed following acidification at the end of sample digestion. This new approach enables the end-to-end one-dimensional liquid chromatography-tandem mass spectrometry (1D LC-MS/MS) workflow (i.e., from sample preparation to HCP identification) to be completed in 7-8 h while demonstrating the ability to consistently identify HCPs across a broad molecular weight range at 10 ppm or above.
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