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一种新型丝素蛋白蛋白融合系统,用于增强纳米抗体在大肠杆菌中的表达。

A novel silk fibroin protein-based fusion system for enhancing the expression of nanobodies in Escherichia coli.

机构信息

CAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No. 189 Songling Road, Qingdao, 266101, China.

University of Chinese Academy of Sciences, No. 19(A) Yuquan Road, Beijing, 100049, China.

出版信息

Appl Microbiol Biotechnol. 2022 Mar;106(5-6):1967-1977. doi: 10.1007/s00253-022-11857-7. Epub 2022 Mar 4.

Abstract

Nanobodies show a great potential in biomedical and biotechnology applications. Bacterial expression is the most widely used expression system for nanobody production. However, the yield of nanobodies is relatively low compared to that of eukaryotic systems. In this study, the repetitive amino acid sequence motifs (GAGAGS) found in silk fibroin protein (SFP) were developed as a novel fusion tag (SF-tag) to enhance the expression of nanobodies in Escherichia coli. SF-tags of 1 to 5 hexapeptide units were fused to the C-terminus of 4G8, a nanobody against human epididymis protein 4 (HE4). The protein yield of 4G8 variants was increased by the extension of hexapeptide units and achieved a 2.5 ~ 7.1-fold increase compared with that of untagged 4G8 (protein yield of 4G8-5C = 0.307 mg/g vs that of untagged 4G8 = 0.043 mg/g). Moreover, the fusion of SF-tags not only had no significant effect on the affinity of 4G8, but also showed a slight increase in the thermal stability of SF-tag-fused 4G8 variants. The fusion of SF-tags increased the transcription of 4G8 by 2.3 ~ 7.0-fold, indicating SF-tags enhanced the protein expression at the transcriptional level. To verify the applicability of the SF-tags for other nanobody expression, we further investigated the protein expression of two other anti-HE4 nanobodies 1G8 and 3A3 upon fusion with the SF-tags. Results indicated that the SF-tags enhanced the protein expression up to 5.2-fold and 5.7-fold for 1G8 and 3A3, respectively. For the first time, this study reported a novel and versatile fusion tag system based on the SFP for improving nanobody expression in Escherichia coli, which may enhance its potential for wider applications.Key points• A silk fibroin protein-based fusion tag (SF-tag) was developed to enhance the expression of nanobodies in Escherichia coli.• The SF-tag enhanced the nanobody expression at the transcriptional level.• The fusion of SF-tag had no significant effect on the affinity of nanobodies and could slightly increase the thermal stability of nanobodies.

摘要

纳米抗体在生物医学和生物技术应用中具有巨大潜力。细菌表达是生产纳米抗体最广泛使用的表达系统。然而,与真核系统相比,纳米抗体的产量相对较低。在这项研究中,发现丝素蛋白(SFP)中的重复氨基酸序列基序(GAGAGS)被开发为一种新的融合标签(SF-tag),以增强纳米抗体在大肠杆菌中的表达。将 1 到 5 个六肽单位的 SF-tag 融合到针对人附睾蛋白 4(HE4)的纳米抗体 4G8 的 C 端。通过扩展六肽单位,4G8 变体的蛋白质产量增加,与未标记的 4G8 相比,实现了 2.5 到 7.1 倍的增加(4G8-5C 的蛋白质产量为 0.307 mg/g,而未标记的 4G8 的蛋白质产量为 0.043 mg/g)。此外,SF-tag 的融合不仅对 4G8 的亲和力没有显著影响,而且还略微增加了 SF-tag 融合的 4G8 变体的热稳定性。SF-tag 的融合将 4G8 的转录增加了 2.3 到 7.0 倍,表明 SF-tag 在转录水平上增强了蛋白质表达。为了验证 SF-tag 对其他纳米抗体表达的适用性,我们进一步研究了融合 SF-tag 后两种其他抗 HE4 纳米抗体 1G8 和 3A3 的蛋白质表达。结果表明,SF-tag 分别将 1G8 和 3A3 的蛋白质表达提高了 5.2 倍和 5.7 倍。这是首次报道了基于 SFP 的新型多功能融合标签系统,用于提高大肠杆菌中纳米抗体的表达,这可能会增强其在更广泛应用中的潜力。关键点:

  • 开发了基于丝素蛋白的融合标签(SF-tag),以增强大肠杆菌中纳米抗体的表达。

  • SF-tag 在转录水平上增强了纳米抗体的表达。

  • SF-tag 的融合对纳米抗体的亲和力没有显著影响,并且可以略微增加纳米抗体的热稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc5b/8894094/f8f919dca34c/253_2022_11857_Fig1_HTML.jpg

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