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生成并功能鉴定抗 FGF2 单克隆抗体 3F12E7 的单链可变片段(scFv)。

Generation and functional characterization of a single-chain variable fragment (scFv) of the anti-FGF2 3F12E7 monoclonal antibody.

机构信息

Department of Biophysics, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - Vila Clementino, São Paulo, SP, CEP 04044-020, Brazil.

Instituto de Biologia, Universidade Estadual de Campinas, Campinas, Brazil.

出版信息

Sci Rep. 2021 Jan 14;11(1):1432. doi: 10.1038/s41598-020-80746-8.

DOI:10.1038/s41598-020-80746-8
PMID:33446839
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7809466/
Abstract

Single-chain variable fragments (scFvs) are small-sized artificial constructs composed of the immunoglobulin heavy and light chain variable regions connected by a peptide linker. We have previously described an anti-fibroblast growth factor 2 (FGF2) immunoglobulin G (IgG) monoclonal antibody (mAb), named 3F12E7, with notable antitumor potential revealed by preclinical assays. FGF2 is a known angiogenesis-associated molecule implicated in tumor progression. In this report, we describe a recombinant scFv format for the 3F12E7 mAb. The results demonstrate that the generated 3F12E7 scFv, although prone to aggregation, comprises an active anti-FGF2 product that contains monomers and small oligomers. Functionally, the 3F12E7 scFv preparations specifically recognize FGF2 and inhibit tumor growth similar to the corresponding full-length IgG counterpart in an experimental model. In silico molecular analysis provided insights into the aggregation propensity and the antigen-recognition by scFv units. Antigen-binding determinants were predicted outside the most aggregation-prone hotspots. Overall, our experimental and prediction dataset describes an scFv scaffold for the 3F12E7 mAb and also provides insights to further engineer non-aggregated anti-FGF2 scFv-based tools for therapeutic and research purposes.

摘要

单链可变片段 (scFv) 是由免疫球蛋白重链和轻链可变区通过肽接头连接而成的小型人工构建体。我们之前描述了一种抗成纤维细胞生长因子 2 (FGF2) 的 IgG 单克隆抗体 (mAb),称为 3F12E7,通过临床前研究显示出显著的抗肿瘤潜力。FGF2 是一种已知的与血管生成相关的分子,与肿瘤进展有关。在本报告中,我们描述了 3F12E7 mAb 的重组 scFv 形式。结果表明,虽然生成的 3F12E7 scFv容易聚集,但它包含一个活性的抗 FGF2 产物,其中包含单体和小寡聚物。在功能上,3F12E7 scFv 制剂特异性识别 FGF2 并抑制肿瘤生长,类似于在实验模型中相应的全长 IgG 对应物。计算分子分析提供了 scFv 单位聚集倾向和抗原识别的见解。抗原结合决定簇预测在最易聚集的热点之外。总的来说,我们的实验和预测数据集描述了 3F12E7 mAb 的 scFv 支架,并为进一步设计用于治疗和研究目的的非聚集抗 FGF2 scFv 工具提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/33b366b26af8/41598_2020_80746_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/467a4c3a32ae/41598_2020_80746_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/7ed6fdbdde87/41598_2020_80746_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/549321da8bbb/41598_2020_80746_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/33b366b26af8/41598_2020_80746_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/467a4c3a32ae/41598_2020_80746_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/7ed6fdbdde87/41598_2020_80746_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/549321da8bbb/41598_2020_80746_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e55/7809466/33b366b26af8/41598_2020_80746_Fig4_HTML.jpg

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