利用刺突蛋白受体结合域作为抗原开发和鉴定多聚体重组蛋白以诱导 SARS-CoV-2 中和作用。

Development and characterization of a multimeric recombinant protein using the spike protein receptor binding domain as an antigen to induce SARS-CoV-2 neutralization.

机构信息

Department of Microbiology, Immunology and Parasitology, Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil.

Department of Biochemistry, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, São Paulo, Brazil.

出版信息

Immun Inflamm Dis. 2024 Jul;12(7):e1353. doi: 10.1002/iid3.1353.

Abstract

BACKGROUND

SARS-CoV2 virus, responsible for the COVID-19 pandemic, has four structural proteins and 16 nonstructural proteins. S-protein is one of the structural proteins exposed on the virus surface and is the main target for producing neutralizing antibodies and vaccines. The S-protein forms a trimer that can bind the angiotensin-converting enzyme 2 (ACE2) through its receptor binding domain (RBD) for cell entry.

AIMS

The goal of this study was to express in HEK293 cells a new RBD recombinant protein in a constitutive and stable manner in order to use it as an alternative immunogen and diagnostic tool for COVID-19.

MATERIALS & METHODS: The protein was designed to contain an immunoglobulin signal sequence, an explanded C-terminal section of the RBD, a region responsible for the bacteriophage T4 trimerization inducer, and six histidines in the pCDNA-3.1 plasmid. Following transformation, the cells were selected with geneticin-G418 and purified from serum-fre culture supernatants using Ni2+-agarand size exclusion chromatography. The protein was structurally identified by cross-linking and circular dichroism experiments, and utilized to immunize mice in conjuction with AS03 or alum adjuvants. The mice sera were examined for antibody recognition, receptor-binding inhibition, and virus neutralization, while spleens were evaluated for γ-interferon production in the presence of RBD.

RESULTS

The protein released in the culture supernatant of cells, and exhibited a molecular mass of 135 kDa with a secondary structure like the monomeric and trimeric RBD. After purification, it formed a multimeric structure comprising trimers and hexamers, which were able to bind the ACE2 receptor. It generated high antibody titers in mice when combined with AS03 adjuvant (up to 1:50,000). The sera were capable of inhibiting binding of biotin-labeled ACE2 to the virus S1 subunit and could neutralize the entry of the Wuhan virus strain into cells at dilutions up to 1:2000. It produced specific IFN-γ producing cells in immunized mouse splenocytes.

DISCUSSION

Our data describe a new RBD containing protein, forming trimers and hexamers, which are able to induce a protective humoral and cellular response against SARS-CoV2.

CONCLUSION

These results add a new arsenal to combat COVID-19, as an alternative immunogen or antigen for diagnosis.

摘要

背景

导致 COVID-19 大流行的 SARS-CoV2 病毒有 4 种结构蛋白和 16 种非结构蛋白。S 蛋白是病毒表面暴露的结构蛋白之一,是产生中和抗体和疫苗的主要目标。S 蛋白形成三聚体,可通过其受体结合域(RBD)与血管紧张素转换酶 2(ACE2)结合,从而进入细胞。

目的

本研究的目的是在 HEK293 细胞中以组成型和稳定的方式表达一种新的 RBD 重组蛋白,将其用作 COVID-19 的替代免疫原和诊断工具。

材料和方法

该蛋白设计含有免疫球蛋白信号序列、RBD 扩展的 C 端部分、负责噬菌体 T4 三聚体诱导的区域和 pCDNA-3.1 质粒中的 6 个组氨酸。转化后,细胞用遗传霉素-G418 选择,并用 Ni2+-agarose 和分子筛从无血清培养上清液中纯化。通过交联和圆二色性实验对蛋白质进行结构鉴定,并与 AS03 或明矾佐剂一起免疫小鼠。检测小鼠血清中抗体的识别、受体结合抑制和病毒中和,同时评估脾细胞在 RBD 存在下产生γ-干扰素的情况。

结果

该蛋白从细胞培养上清液中释放,具有 135kDa 的分子量,具有单体和三聚体 RBD 的二级结构。纯化后,它形成了一种多聚体结构,包括三聚体和六聚体,能够与 ACE2 受体结合。当与 AS03 佐剂结合时,它在小鼠中产生了高抗体滴度(高达 1:50,000)。血清能够抑制生物素标记的 ACE2 与病毒 S1 亚基的结合,并能够在稀释度高达 1:2000 时抑制武汉病毒株进入细胞。它在免疫小鼠脾细胞中产生了特异性 IFN-γ产生细胞。

讨论

我们的数据描述了一种新的包含 RBD 的蛋白,形成三聚体和六聚体,能够诱导针对 SARS-CoV2 的保护性体液和细胞反应。

结论

这些结果为抗击 COVID-19 提供了一种新的武器,可作为替代免疫原或抗原用于诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b27/11273545/6ae37ddb70a1/IID3-12-e1353-g006.jpg

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