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