利用针对蛋白转化酶(PPC)裂解位点的 Fv 抗体预防 SARS-CoV-2 感染

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics
MedChemComm Pub Date : 2024-08-26 DOI:10.1039/D4MD00552J
Jaeyong Jung, Jeong Soo Sung, Soonil Kwon, Hyung Eun Bae, Min-Jung Kang, Joachim Jose, Misu Lee and Jae-Chul Pyun
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引用次数: 0

摘要

从 Fv 抗体库中筛选出了以 SARS-CoV-2 穗状病毒(SP)的蛋白转化酶(PPC)区为靶点的 Fv 抗体,以抑制 SARS-CoV-2 感染。筛选出的两种 Fv 抗体被表达为可溶性重组蛋白,并使用表面等离子体共振生物传感器评估了它们的结合亲和力。这些Fv-抗体的结合区域与呋喃蛋白(S1/S2)和跨膜丝氨酸蛋白酶2(TMPRSS2,S2′)的裂解位点相对应。使用携带四种不同 SARS-CoV-2 变体 SP 的假病毒(野生型 (D614)、delta (B.1.617.2)、ocmicron (BA.2) 和 omicron (BA.4/5))进行细胞感染试验,证明了这两种 Fv 抗体的中和活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preventing SARS-CoV-2 infection using Fv-antibodies targeting the proprotein convertase (PPC) cleavage site

Preventing SARS-CoV-2 infection using Fv-antibodies targeting the proprotein convertase (PPC) cleavage site

Preventing SARS-CoV-2 infection using Fv-antibodies targeting the proprotein convertase (PPC) cleavage site

Fv-antibodies targeting the proprotein convertase (PPC) region of the SARS-CoV-2 spike protein (SP) were screened from an Fv-antibody library to inhibit SARS-CoV-2 infection. Two selected Fv-antibodies were expressed as soluble recombinant proteins, and their binding affinities were assessed using a surface plasmon resonance biosensor. The binding regions of these Fv-antibodies corresponded to the cleavage sites of furin (S1/S2) and transmembrane serine protease 2 (TMPRSS2, S2′). The neutralizing activities of the two Fv-antibodies were demonstrated using a cell-based infection assay with pseudo-viruses carrying the SP of four different SARS-CoV-2 variants: wild-type (D614), delta (B.1.617.2), omicron (BA.2), and omicron (BA.4/5).

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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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