Suppr超能文献

重组人乳头瘤病毒 16 L1 蛋白与 -叠氮基-苯丙氨酸的工程化。

Engineering of Recombinant Human Papillomavirus 16 L1 Protein for Incorporation with -Azido--Phenylalanine.

机构信息

Department of Biotechnology and Bioengineering, Chonnam National University, Gwangju 61186, Republic of Korea.

Department of Chemical and Biomolecular Engineering, KAIST, Daejeon 34141, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2024 Sep 28;34(9):1926-1932. doi: 10.4014/jmb.2407.07033. Epub 2024 Aug 9.

Abstract

Human papillomavirus (HPV) L1 capsid protein were produced in several host systems, but few studies have focused on enhancing the properties of the L1 protein. In this study, we aimed to produce recombinant Human papillomavirus (HPV) L1 capsid protein containing -azido--phenylalanine (pAzF) in . First, we expressed the maltose-binding protein (MBP)-fused HPV16 L1, and 5 residues in HPV16 L1 protein were selected by the in silico modeling for amber codon substitution. Among the variants of the five locations, we identified a candidate that exhibited significant differences in expression with and without pAzF via genetic code expansion (GCE). The expressed recombinant MBP-HPV16L1 protein was confirmed for incorporation of pAzF and the formation of VLPs was tested in vitro.

摘要

人乳头瘤病毒 (HPV) L1 衣壳蛋白在多种宿主系统中被生产出来,但很少有研究集中在增强 L1 蛋白的特性上。在这项研究中,我们旨在生产含有 -叠氮基苯丙氨酸 (pAzF) 的重组人乳头瘤病毒 (HPV) L1 衣壳蛋白。首先,我们表达了麦芽糖结合蛋白 (MBP) 融合的 HPV16 L1,通过计算机建模选择了 HPV16 L1 蛋白中的 5 个残基进行琥珀终止密码子替换。在这 5 个位置的变体中,我们通过遗传密码扩展 (GCE) 鉴定了一个候选变体,该变体在有无 pAzF 的情况下表达差异显著。表达的重组 MBP-HPV16L1 蛋白被证实掺入了 pAzF,并且在体外测试了 VLPs 的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f55/11473617/59e2da010040/jmb-34-9-1926-f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验