Istituto di Biostrutture e Bioimmagini, CNR, Via Mezzocannone 16, 80134, Napoli, Italy.
Dipartimento di Scienze e Tecnologie Ambientali, Biologiche e Farmaceutiche, Università della Campania "L. Vanvitelli", Via Vivaldi, 43, 81100, Caserta, Italy.
Mol Biotechnol. 2019 Jul;61(7):513-520. doi: 10.1007/s12033-019-00181-7.
VEGF-A/VEGFR2 complex is the major signaling pathway involved in angiogenesis and the inhibition of this axis retards tumor growth and inflammatory disorders progression, reducing vessel sprouting. Signaling by VEGFR2 requires receptor dimerization and a well-defined orientation of monomers in the active dimer. The extracellular portion of receptor is composed of seven Ig-like domains, of which D2-3 are the ligand binding domains, while D4 and D7, establishing homotypic contacts, allosterically regulate receptor activity. The allosteric targeting of VEGFR2 represents a promising alternative to study neovascular disorders overcoming drawbacks related to competition with VEGF. In this work, we expressed in bacterial host domain 4 of VEGFR2 (VEGFR2D4). After protein refolding, we characterized the purified domain and administered it in mice for monoclonal antibodies production. One of them, mAbD4, was tested in ELISA assays, showing a nanomolar affinity for VEGFR2D4. Finally, the methodology here described could contribute to the development of antibodies which can allosterically bind VEGFR2 and therefore to be used for imaging purposes or to modulate receptor signaling.
VEGF-A/VEGFR2 复合物是参与血管生成的主要信号通路,抑制该轴可减缓肿瘤生长和炎症性疾病的进展,减少血管生成。VEGFR2 的信号转导需要受体二聚化和单体在活性二聚体中的明确取向。受体的细胞外部分由七个 Ig 样结构域组成,其中 D2-3 是配体结合结构域,而 D4 和 D7 通过形成同源接触,别构调节受体活性。VEGFR2 的变构靶向是一种很有前途的替代方法,可以研究新血管生成疾病,克服与 VEGF 竞争相关的缺点。在这项工作中,我们在细菌宿主中表达了 VEGFR2 的结构域 4(VEGFR2D4)。在蛋白质重折叠后,我们对纯化的结构域进行了表征,并将其用于小鼠单克隆抗体的生产。其中一种单克隆抗体 mAbD4 在 ELISA 测定中表现出对 VEGFR2D4 的纳摩尔亲和力。最后,这里描述的方法可以促进开发能够变构结合 VEGFR2 的抗体,从而用于成像目的或调节受体信号。