蛋白酶
背景(考古学)
细胞因子
分泌物
促炎细胞因子
药物发现
计算生物学
生物
细胞生物学
免疫学
炎症
生物信息学
生物化学
酶
古生物学
作者
Carlos A. Aldrete,Connor C. Call,Lucas E. Sant’Anna,Alexander E. Vlahos,Jimin Pei,Qian Cong,Xiaojing Gao
标识
DOI:10.1101/2024.01.18.576308
摘要
Abstract Synthetic circuits that regulate protein secretion in human cells could support cell-based therapies by enabling control over local environments. While protein-level circuits enable such potential clinical applications, featuring orthogonality and compactness, their non-human origin poses a potential immunogenic risk. Here, we developed Humanized Drug Induced Regulation of Engineered CyTokines (hDIRECT) as a platform to control cytokine activity exclusively using human-derived proteins. We sourced a specific human protease and its FDA-approved inhibitor. We engineered cytokines (IL-2, IL-6, and IL-10) whose activities can be activated and abrogated by proteolytic cleavage. We utilized species specificity and re-localization strategies to orthogonalize the cytokines and protease from the human context that they would be deployed in. hDIRECT should enable local cytokine activation to support a variety of cell-based therapies such as muscle regeneration and cancer immunotherapy. Our work offers a proof of concept for the emerging appreciation of humanization in synthetic biology for human health.
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