整合素
溶酶体
细胞生物学
嵌合体(遗传学)
蛋白质降解
化学
细胞外
癌细胞
生物
生物化学
癌症
受体
基因
酶
遗传学
作者
Yaxian Zhou,Yaxian Liao,Yuan Zhao,Weiping Tang
标识
DOI:10.1002/cmdc.202300643
摘要
The emerging of lysosomal targeting chimera (LYTAC) expands the field of targeted protein degradation (TPD) to include the extracellular proteins for precise depletion. However, most of the reported LYTACs either induce ubiquitous degradation of the protein of interest (POI) in a broad range of tissues or specifically target liver cells. More tissue‐selective degraders are highly desirable. Herein, we describe the development of cyclic RGD (cRGD) peptide‐antibody conjugates as a novel class of integrin targeting chimeras (ITACs) with potential cancer selectivity. Our results indicate that the ITACs are able to recruit integrin to induce the degradation of both soluble and membrane targets in the lysosome. We observed higher efficiency of ITACs on degrading membrane protein in cancer cells, providing a promising platform for cancer‐selective TPD strategy.
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