Development of Integrin Targeting Chimeras (ITACs) for the Lysosomal Degradation of Extracellular Proteins.

IF 3.6 4区 医学 Q2 CHEMISTRY, MEDICINAL
ChemMedChem Pub Date : 2024-09-08 DOI:10.1002/cmdc.202300643
Yaxian Zhou, Yaxian Liao, Yuan Zhao, Weiping Tang
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引用次数: 0

Abstract

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.

开发用于细胞外蛋白质溶酶体降解的整合素靶向嵌合体 (ITAC)。
溶酶体靶向嵌合体(LYTAC)的出现扩大了靶向蛋白质降解(TPD)的领域,将细胞外蛋白质也包括在内,以实现精确降解。然而,大多数已报道的 LYTAC 要么能在广泛的组织中诱导相关蛋白(POI)的普遍降解,要么能特异性地靶向肝细胞。我们非常需要更具组织选择性的降解剂。在此,我们介绍了环RGD(cRGD)肽-抗体共轭物的开发情况,这是一类新型整合素靶向嵌合体(ITACs),具有潜在的癌症选择性。我们的研究结果表明,ITACs 能够招募整合素,诱导溶酶体中可溶性和膜靶标的降解。我们观察到 ITACs 降解癌细胞膜蛋白的效率更高,为癌症选择性 TPD 策略提供了一个前景广阔的平台。
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来源期刊
ChemMedChem
ChemMedChem 医学-药学
CiteScore
6.70
自引率
2.90%
发文量
280
审稿时长
1 months
期刊介绍: Quality research. Outstanding publications. With an impact factor of 3.124 (2019), ChemMedChem is a top journal for research at the interface of chemistry, biology and medicine. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. ChemMedChem publishes primary as well as critical secondary and tertiary information from authors across and for the world. Its mission is to integrate the wide and flourishing field of medicinal and pharmaceutical sciences, ranging from drug design and discovery to drug development and delivery, from molecular modeling to combinatorial chemistry, from target validation to lead generation and ADMET studies. ChemMedChem typically covers topics on small molecules, therapeutic macromolecules, peptides, peptidomimetics, and aptamers, protein-drug conjugates, nucleic acid therapies, and beginning 2017, nanomedicine, particularly 1) targeted nanodelivery, 2) theranostic nanoparticles, and 3) nanodrugs. Contents ChemMedChem publishes an attractive mixture of: Full Papers and Communications Reviews and Minireviews Patent Reviews Highlights and Concepts Book and Multimedia Reviews.
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