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分泌信号的正交化人类蛋白酶控制

Orthogonalized human protease control of secreted signals.

作者信息

Aldrete Carlos A, Call Connor C, Sant'Anna Lucas E, Vlahos Alexander E, Pei Jimin, Cong Qian, Gao Xiaojing J

机构信息

Department of Chemical Engineering, Stanford University, Stanford CA 94305, USA.

Department of Bioengineering, Stanford University, Stanford CA 94305, USA.

出版信息

bioRxiv. 2024 Oct 21:2024.01.18.576308. doi: 10.1101/2024.01.18.576308.

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.

摘要

能够调节人类细胞中蛋白质分泌的合成回路,可通过实现对局部环境的控制来支持基于细胞的疗法。虽然蛋白质水平的回路具备正交性和紧凑性等潜在临床应用特性,但其非人类来源带来了潜在的免疫原性风险。在此,我们开发了人源化药物诱导工程细胞因子调控(hDIRECT)平台,以专门利用源自人类的蛋白质来控制细胞因子活性。我们获取了一种特定的人类蛋白酶及其经美国食品药品监督管理局批准的抑制剂。我们设计了细胞因子(白细胞介素 -2、白细胞介素 -6 和白细胞介素 -10),其活性可通过蛋白水解切割来激活和消除。我们利用物种特异性和重新定位策略,使细胞因子和蛋白酶与它们将被应用的人类环境正交。hDIRECT 应能实现局部细胞因子激活,以支持多种基于细胞的疗法,如肌肉再生和癌症免疫疗法。我们的工作为合成生物学中对人类健康进行人源化的新认识提供了概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e59f/11526856/86703792b210/nihpp-2024.01.18.576308v2-f0001.jpg

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