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一种双环肽神经纤毛蛋白-1(NP-1)拮抗剂(EG3287)的特性揭示了血管内皮生长因子第8外显子对NP-1结合的重要性以及NP-1在KDR信号传导中的作用。

Characterization of a bicyclic peptide neuropilin-1 (NP-1) antagonist (EG3287) reveals importance of vascular endothelial growth factor exon 8 for NP-1 binding and role of NP-1 in KDR signaling.

作者信息

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

机构信息

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.

出版信息

J Biol Chem. 2006 May 12;281(19):13493-13502. doi: 10.1074/jbc.M512121200. Epub 2006 Mar 2.

Abstract

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.

摘要

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。

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