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工程化 CRISPR/Cas9 用于多重重组凝血因子生产。

Engineering CRISPR/Cas9 for Multiplexed Recombinant Coagulation Factor Production.

机构信息

Department of Pediatrics, Division of Blood and Marrow Transplantation, MMC 366 Mayo, 8366A, 420 Delaware Street SE, Minneapolis, MN 55455, USA.

Department of General Surgery, Madigan Army Medical Center, 9040 Jackson Ave., Tacoma, WA 98431, USA.

出版信息

Int J Mol Sci. 2022 May 3;23(9):5090. doi: 10.3390/ijms23095090.

Abstract

Current hemostatic agents are obtained from pooled plasma from multiple donors requiring costly pathogen screening and processing. Recombinant DNA-based production represents an engineering solution that could improve supply, uniformity, and safety. Current approaches are typically for single gene candidate peptides and often employ non-human cells. We devised an approach where multiple gene products could be produced from a single population of cells. We identified gene specific Synergistic Activation Mediators (SAM) from the CRISPR/Cas9 system for targeted overexpression of coagulation factors II, VII, IX, X, and fibrinogen. The components of the CRISPR-SAM system were expressed in Human Embryonic Kidney Cells (HEK293), and single (singleplex) or multi-gene (multiplex) upregulation was assessed by quantitative RT-PCR (qRT-PCR) and protein expression by ELISA analysis. Factor II, VII, IX, and X singleplex and multiplex activation resulted in 120-4700-fold and 60-680-fold increases in gene expression, respectively. Fibrinogen sub-unit gene activation resulted in a 1700-92,000-fold increases and 80-5500-fold increases in singleplex or multiplex approaches, respectively. ELISA analysis showed a concomitant upregulation of candidate gene products. Our findings demonstrate the capability of CRISPR/Cas9 SAMs for single or multi-agent production in human cells and represent an engineering advance that augments current recombinant peptide production techniques.

摘要

目前的止血剂是从多个供体的混合血浆中获得的,这需要昂贵的病原体筛选和处理。基于重组 DNA 的生产代表了一种工程解决方案,可以提高供应、一致性和安全性。目前的方法通常是针对单个基因候选肽,并且经常使用非人类细胞。我们设计了一种方法,可以从单个细胞群体中产生多种基因产物。我们从 CRISPR/Cas9 系统中鉴定出基因特异性协同激活调节剂 (SAM),用于靶向过表达凝血因子 II、VII、IX、X 和纤维蛋白原。CRISPR-SAM 系统的组件在人胚肾细胞 (HEK293) 中表达,并通过定量 RT-PCR (qRT-PCR) 和 ELISA 分析评估单基因 (单重) 或多基因 (多重) 上调。因子 II、VII、IX 和 X 的单重和多重激活分别导致基因表达增加 120-4700 倍和 60-680 倍。纤维蛋白原亚基基因激活分别导致单重或多重方法的基因表达增加 1700-92000 倍和 80-5500 倍。ELISA 分析显示候选基因产物的同时上调。我们的研究结果表明 CRISPR/Cas9 SAM 具有在人类细胞中单或多剂生产的能力,代表了一种工程上的进步,增强了当前的重组肽生产技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3723/9100926/88f9ff80d4a1/ijms-23-05090-g0A1.jpg

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