用于癌症治疗的重组人白细胞介素-37 的重组表达、下游优化和治疗评估。

IF 2 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Biotechnology Letters Pub Date : 2024-12-01 Epub Date: 2024-10-18 DOI:10.1007/s10529-024-03539-3
Zaheer Abbas, Samia Afzal, Nao Akusa Fujimura, Muhammad Akram, Saad Tahir, Kausar Malik, Nadeem Ahmed
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引用次数: 0

摘要

白细胞介素-37 是一种具有强效免疫抑制特性的细胞因子,已被证明具有治疗自身免疫性疾病、慢性炎症性疾病以及某些类型癌症的潜力。IL-37 是一种 19 kDa 蛋白质,可通过依赖受体和不依赖受体的途径与蛋白质相互作用。在与 Rosetta-gami 2(DE3) 和 Rosetta 2(DE3) pLysS 的表达进行比较后,在 Rosetta 2(DE3) 中优化了克隆到 pET-28a 载体中的 IL-37 蛋白的表达,然后将其用于 IL-37 的大规模生产。通过 IMAC 纯化 IL-37,自诱导发酵产生的 0.9 mg/mL 蛋白纯度大于 97%。IL-37 蛋白的 IC50 值为 100 µg/mL IL-37 蛋白可抑制 80% 的癌细胞。由于IL-37的IC50值与多柔比星相当,因此它可能是一种很有前途的癌症治疗靶标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recombinant expression, downstream optimization, and therapeutic evaluation of recombinant human interleukin-37 for cancer therapy.

Interleukin-37 is a cytokine with potent immunosuppressive properties that has been shown to have potential to treat autoimmune and chronic inflammatory diseases, as well as certain types of cancer. IL-37 is a 19 kDa protein which interacts with proteins in receptor-dependent and receptor-independent pathways. The expression of the IL-37 protein cloned into the pET-28a vector was optimized in Rosetta 2(DE3) after comparing its expression with Rosetta-gami 2(DE3) and Rosetta 2(DE3) pLysS, which was then used for the large-scale production of IL-37. IMAC purification of IL-37 yielded > 97% pure 0.9 mg/mL protein from auto-induced fermentation. The IC50 value of IL-37 was < 1 µM, which was similar to that of doxorubicin, and proliferation of > 80% of all cancer cells was inhibited by 100 µg/mL of IL-37 protein. IL-37 may be a promising theragnostic target for cancer due to its comparable IC50 value with that of doxorubicin.

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来源期刊
Biotechnology Letters
Biotechnology Letters 工程技术-生物工程与应用微生物
CiteScore
5.90
自引率
3.70%
发文量
108
审稿时长
1.2 months
期刊介绍: Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them. All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included. Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields. The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories. Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.
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