[Capsid Protein of Bacteriophage Beihai32 as a Platform for Construction of Virus-Like Particles Displaying Foreign Polypeptides].

Q3 Medicine
A A Zykova, E S Mardanova, E A Blokhina, N V Ravin
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引用次数: 0

Abstract

Virus-like particles (VLPs) can be used as nanosized carriers for the presentation of various peptides, including antigens. VLPs formed by self-assembly from capsid proteins of bacteriophages with singlestranded RNA genomes can be obtained in bacterial expression systems. However, to act as a universal platform for antigen presentation, the carrier protein should retain the ability to self-assemble into VLPs upon attachment of long peptides. We have shown that the capsid protein of the bacteriophage Beihai32 can be used as a carrier of peptides at least 238 amino acid residues long. The hybrid capsid protein, to which green fluorescent protein (GFP) was attached at the C-terminus, was expressed in Escherichia coli cells and formed spherical VLPs with a diameter of about 30 nm in vivo. GFP was localized on the surface of these particles and retained the ability to fluoresce. Thus, the bacteriophage Beihai32 capsid protein is an effective platform for constructing VLPs that present long peptide antigens on their surface, and such VLPs can be the basis for new recombinant vaccines.

噬菌体北海32的衣壳蛋白作为构建外源多肽类病毒颗粒的平台。
病毒样颗粒(vlp)可以用作纳米级载体,用于呈现各种肽,包括抗原。噬菌体衣壳蛋白与单链RNA基因组自组装形成的VLPs可以在细菌表达系统中获得。然而,为了作为抗原呈递的通用平台,载体蛋白应该保留在长肽附着后自组装成VLPs的能力。我们已经证明噬菌体北海32的衣壳蛋白可以作为至少238个氨基酸残基长的肽的载体。c端附着绿色荧光蛋白(GFP)的杂交衣壳蛋白在大肠杆菌细胞中表达,在体内形成直径约30 nm的球形VLPs。GFP被定位在这些颗粒的表面,并保留了荧光的能力。因此,噬菌体北海32衣壳蛋白是构建在其表面呈递长肽抗原的VLPs的有效平台,这种VLPs可以作为新的重组疫苗的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molekulyarnaya Biologiya
Molekulyarnaya Biologiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
131
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