结合
组织蛋白酶
体外
化学
有效载荷(计算)
生物化学
计算生物学
分解代谢
酶
计算机科学
生物
数学
计算机网络
数学分析
网络数据包
作者
Andrew J. Bessire,Chakrapani Subramanyam
出处
期刊:Methods in molecular biology
日期:2019-10-24
卷期号:: 341-351
被引量:4
标识
DOI:10.1007/978-1-4939-9929-3_24
摘要
A critical component of antibody-drug conjugate (ADC) development is identification or verification of the active released entity upon cellular uptake and exposure to lysosomal enzymes. Coupled with LC/MS, commercial human lysosomal preparations can be used as an in vitro tool to explore the release characteristics of new ADCs, and gain information on potential metabolic or chemical liabilities of new payload structures. A general method for approaching this is described for cathepsin B-cleavable as well as non-cleavable ADCs, and opportunities for tailoring the method to specific cases are indicated.
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