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可溶性干扰素-α的生产策略及其在虫媒病毒和SARS-CoV-2中的潜在应用

Strategies for the Production of Soluble Interferon-Alpha and Potential Application in Arboviruses and SARS-CoV-2.

作者信息

Grabarz Felipe, Lopes Alexandre Paulo Yague, Barbosa Flávia Ferreira, Barazzone Giovana Cappio, Santos Jademilson Celestino, Botosso Viviane Fongaro, Jorge Soraia Attie Calil, Nascimento Ana Lucia Tabet Oller, Astray Renato Mancini, Gonçalves Viviane Maimoni

机构信息

Laboratório de Desenvolvimento de Vacinas, Instituto Butantan, São Paulo 05503-900, Brazil.

Programa Interunidades em Biotecnologia, Universidade de São Paulo, São Paulo 05508-060, Brazil.

出版信息

Life (Basel). 2021 May 21;11(6):460. doi: 10.3390/life11060460.

Abstract

Biopharmaceutical production is currently a multibillion-dollar industry with high growth perspectives. The research and development of biologically sourced pharmaceuticals are extremely important and a reality in our current healthcare system. Interferon alpha consensus (cIFN) is a non-natural synthetic antiviral molecule that comprises all the most prevalent amino acids of IFN-α into one consensus protein sequence. For clinical use, cIFN is produced in in the form of inclusion bodies. Here, we describe the use of two solubility tags (Fh8 and DsbC) to improve soluble cIFN production. Furthermore, we analyzed cIFN production in different culture media and temperatures in order to improve biopharmaceutical production. Our results demonstrate that Fh8-cIFN yield was improved when bacteria were cultivated in autoinduction culture medium at 30 °C. After hydrolysis, the recovery of soluble untagged cIFN was 58% from purified Fh8-cIFN molecule, fourfold higher when compared to cIFN recovered from the DsbC-cIFN, which achieved 14% recovery. The biological activity of cIFN was tested on in vitro model of antiviral effect against Zika, Mayaro, Chikungunya and SARS-CoV-2 virus infection in susceptible VERO cells. We show, for the first time, that cIFN has a potent activity against these viruses, being very low amounts of the molecule sufficient to inhibit virus multiplication. Thus, this molecule could be used in a clinical approach to treat Arboviruses and SARS-CoV-2.

摘要

生物制药生产目前是一个具有高增长前景的数十亿美元产业。生物源药物的研发极其重要,并且在我们当前的医疗保健系统中已成为现实。干扰素α共识序列(cIFN)是一种非天然合成抗病毒分子,它将IFN-α的所有最常见氨基酸整合到一个共识蛋白序列中。对于临床应用,cIFN以包涵体的形式产生。在此,我们描述了使用两种溶解性标签(Fh8和DsbC)来提高可溶性cIFN的产量。此外,我们分析了在不同培养基和温度下cIFN的生产情况,以提高生物制药产量。我们的结果表明,当细菌在30°C的自诱导培养基中培养时,Fh8-cIFN的产量得到提高。水解后,从纯化的Fh8-cIFN分子中回收的可溶性无标签cIFN为58%,与从DsbC-cIFN中回收的cIFN相比高出四倍,后者的回收率为14%。在易感VERO细胞中针对寨卡病毒、马亚罗病毒、基孔肯雅病毒和SARS-CoV-2病毒感染的抗病毒作用体外模型上测试了cIFN的生物活性。我们首次表明,cIFN对这些病毒具有强大的活性,极少量的该分子就足以抑制病毒增殖。因此,该分子可用于临床治疗虫媒病毒和SARS-CoV-2。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f493/8223780/40d922367a39/life-11-00460-g001.jpg

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