生物分析
单克隆抗体
色谱法
化学
药效学
脑脊液
药物发现
细胞外
人脑
药理学
计算生物学
τ蛋白
抗体
神经科学
医学
阿尔茨海默病
药代动力学
疾病
生物
内科学
免疫学
生物化学
作者
Wade Self,Khader Awwad,John P. Savaryn,Michael Schulz
出处
期刊:Cold Spring Harbor Laboratory - medRxiv
日期:2021-05-10
标识
DOI:10.1101/2021.05.10.21252513
摘要
Abstract Aims Tau protein is a key target of interest in developing therapeutics for neurodegenerative diseases. Here, we sought to develop a method that quantifies extracellular tau protein concentrations human cerebrospinal fluid (CSF) without antibody-based enrichment strategies. Results We demonstrate that the fit-for-purpose validated method in Alzheimer’s Disease CSF is limited to quasi quantitative measures of tau surrogate peptides. We also provide evidence that CSF total Tau measures by LC-MS are feasible in the presence of monoclonal therapeutic antibodies in human CSF. Conclusion Our Tau LC-MS/MS method is a translational bioanalytical tool for assaying target engagement and pharmacodynamics for anti-tau antibody drug development campaigns.
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