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Engineering of a Human Vaginal Lactobacillus Strain for Surface Expression of Two-Domain CD4 Molecules▿

机译:人阴道乳酸菌菌株用于两域CD4分子表面表达的工程▿

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摘要

Women are at significant risk of heterosexually transmitted human immunodeficiency virus (HIV) infection, with the mucosal epithelium of the cervix and vagina serving as a major portal of entry. The cervicovaginal mucosa naturally harbors dynamic microflora composed predominantly of lactobacilli, which may be genetically modified to serve as a more efficient protective barrier against the heterosexual transmission of HIV. We selected a vaginal strain of Lactobacillus, L. jensenii 1153, for genetic modification to display surface-anchored anti-HIV proteins. Genomic sequencing analyses revealed that L. jensenii 1153 encodes several unique high-molecular-weight cell wall-anchored proteins with a C-terminal cell wall sorting LPQTG motif. In this report, we employed these proteins to express a surface-anchored two-domain CD4 (2D CD4) molecule in L. jensenii 1153. Our studies indicated that the C-terminal cell wall sorting signal LPQTG motif alone is insufficient to drive the surface expression of heterologous proteins, and the display of surface-anchored 2D CD4 molecules required native sequences of a defined length upstream of the unique C-terminal LPQTG cell wall sorting signal and the positively charged C terminus in a Lactobacillus-based expression system. The modified L. jensenii strain displayed 2D CD4 molecules that were uniformly distributed on bacterial surfaces. The surface-anchored 2D CD4 molecule was recognized by a conformation-dependent anti-CD4 antibody, suggesting that the expressed proteins adopted a native conformation. The establishment of this Lactobacillus-based surface expression system, with potential broad applicability, represents a major step toward developing an inexpensive yet durable approach to topical microbicides for the mitigation of heterosexual transmission of HIV and other mucosally transmitted viral pathogens.
机译:妇女面临着异性传播的人类免疫缺陷病毒(HIV)感染的巨大风险,宫颈和阴道的粘膜上皮是进入的主要门户。宫颈阴道粘膜自然含有主要由乳杆菌组成的动态菌群,可对其进行基因修饰以作为针对HIV异性传播的更有效的保护性屏障。我们选择了乳酸杆菌L. jensenii 1153的阴道菌株进行基因修饰,以显示表面锚定的抗HIV蛋白。基因组测序分析表明,詹氏乳杆菌1153编码具有C端细胞壁分选LPQTG基序的几种独特的高分子量细胞壁锚定蛋白。在本报告中,我们利用这些蛋白质在詹森氏菌1153中表达表面锚定的两个结构域CD4(2D CD4)分子。我们的研究表明,仅C端细胞壁分选信号LPQTG基序不足以驱动表面异源蛋白的表达,以及表面锚定的2D CD4分子的展示,需要在基于乳酸杆菌的表达系统中,独特C端LPQTG细胞壁分选信号和带正电的C末端上游具有确定长度的天然序列。改良的詹氏乳杆菌菌株显示了二维CD4分子,它们均匀分布在细菌表面。表面锚定的2D CD4分子被构象依赖性抗CD4抗体识别,表明表达的蛋白质采用了天然构象。具有潜在的广泛应用性的这种基于乳酸杆菌的表面表达系统的建立,是朝着开发廉价而持久的局部杀微生物剂的方法迈出了重要的一步,以减轻HIV和其他粘膜传播的病毒病原体的异性传播。

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