Jia Haiyan, Bagherzadeh Azadeh, Hartzoulakis Basil, Jarvis Ashley, Löhr Marianne, Shaikh Shaheda, Aqil Rehan, Cheng Lili, Tickner Michelle, Esposito Diego, Harris Richard, Driscoll Paul C, Selwood David L, Zachary Ian C
Centre for Cardiovascular Biology and Medicine, Department of Medicine, University College London, London WC1E 6JJ, United Kingdom; Ark Therapeutics Limited, The Rayne Institute, University College London, London WC1E 6JJ, United Kingdom.
NCE Discovery Ltd., Cambridge CB4 0PA, United Kingdom.
J Biol Chem. 2006 May 12;281(19):13493-13502. doi: 10.1074/jbc.M512121200. Epub 2006 Mar 2.
Neuropilin-1 (NP-1) is a receptor for vascular endothelial growth factor-A165 (VEGF-A165) in endothelial cells. To define the role of NP-1 in the biological functions of VEGF, we developed a specific peptide antagonist of VEGF binding to NP-1 based on the NP-1 binding site located in the exon 7- and 8-encoded VEGF-A165 domain. The bicyclic peptide, EG3287, potently (K(i) 1.2 microM) and effectively (>95% inhibition at 100 microM) inhibited VEGF-A165 binding to porcine aortic endothelial cells expressing NP-1 (PAE/NP-1) and breast carcinoma cells expressing only NP-1 receptors for VEGF-A, but had no effect on binding to PAE/KDR or PAE/Flt-1. Molecular dynamics calculations, a nuclear magnetic resonance structure of EG3287, and determination of stability in media, indicated that it constitutes a stable subdomain very similar to the corresponding region of native VEGF-A165. The C terminus encoded by exon 8 and the three-dimensional structure were both critical for EG3287 inhibition of NP-1 binding, whereas modifications at the N terminus had little effect. Although EG3287 had no direct effect on VEGF-A165 binding to KDR receptors, it inhibited cross-linking of VEGF-A165 to KDR in human umbilical vein endothelial cells co-expressing NP-1, and inhibited stimulation of KDR and PLC-gamma tyrosine phosphorylation, activation of ERKs1/2 and prostanoid production. These findings characterize the first specific antagonist of VEGF-A165 binding to NP-1 and demonstrate that NP-1 is essential for optimum KDR activation and intracellular signaling. The results also identify a key role for the C-terminal exon 8 domain in VEGF-A165 binding to NP-1.
神经纤毛蛋白-1(NP-1)是内皮细胞中血管内皮生长因子-A165(VEGF-A165)的受体。为了确定NP-1在VEGF生物学功能中的作用,我们基于位于外显子7和8编码的VEGF-A165结构域中的NP-1结合位点,开发了一种VEGF与NP-1结合的特异性肽拮抗剂。双环肽EG3287能有效(K(i)为1.2微摩尔)且高效(在100微摩尔时抑制率>95%)地抑制VEGF-A165与表达NP-1的猪主动脉内皮细胞(PAE/NP-1)以及仅表达VEGF-A的NP-1受体的乳腺癌细胞的结合,但对与PAE/KDR或PAE/Flt-1的结合没有影响。分子动力学计算、EG3287的核磁共振结构以及在培养基中的稳定性测定表明,它构成了一个与天然VEGF-A165相应区域非常相似的稳定亚结构域。外显子8编码的C末端和三维结构对EG3287抑制NP-1结合都至关重要,而N末端的修饰影响很小。尽管EG3287对VEGF-A165与KDR受体的结合没有直接影响,但它抑制了VEGF-A165与人脐静脉内皮细胞中共表达的NP-1交联到KDR,并抑制了KDR和PLC-γ酪氨酸磷酸化的刺激、ERK1/2的激活以及前列腺素的产生。这些发现表征了VEGF-A165与NP-1结合的首个特异性拮抗剂,并证明NP-1对于最佳KDR激活和细胞内信号传导至关重要。结果还确定了VEGF-A165与NP-1结合中C末端外显子8结构域的关键作用。