Department of Functional and Morphological Science, Faculty of Medicine and Pharmacy, Dunarea de Jos University, 800010 Galati, Romania.
Faculty of Chemistry, Alexandru Ioan Cuza University of Iasi, 11 Carol 1st Bvd, 700506 Iasi, Romania.
Int J Mol Sci. 2024 Jul 16;25(14):7787. doi: 10.3390/ijms25147787.
The kinase pathway plays a crucial role in blood vessel function. Particular attention is paid to VEGFR type 2 angiogenesis and vascular morphogenesis as the tyrosine kinase pathway is preferentially activated. In silico studies were performed on several peptides that affect VEGFR2 in both stimulating and inhibitory ways. This investigation aims to examine the molecular properties of VEGFR2, a molecule primarily involved in the processes of vasculogenesis and angiogenesis. These relationships were defined by the interactions between Vascular Endothelial Growth Factor receptor 2 (VEGFR2) and the structural features of the systems. The chemical space of the inhibitory peptides and stimulators was described using topological and energetic properties. Furthermore, chimeric models of stimulating and inhibitory proteins (for VEGFR2) were computed using the protein system structures. The interaction between the chimeric proteins and VEGFR was computed. The chemical space was further characterized using complex manifolds and high-dimensional data visualization. The results show that a slightly similar chemical area is shared by VEGFR2 and stimulating and inhibitory proteins. On the other hand, the stimulator peptides and the inhibitors have distinct chemical spaces.
激酶通路在血管功能中起着至关重要的作用。特别关注 VEGFR 型 2 血管生成和血管形态发生,因为酪氨酸激酶通路被优先激活。对几种以刺激和抑制方式影响 VEGFR2 的肽进行了计算机模拟研究。本研究旨在研究主要参与血管生成和血管生成过程的血管内皮生长因子受体 2(VEGFR2)的分子特性。这些关系是通过血管内皮生长因子受体 2(VEGFR2)与系统结构特征之间的相互作用来定义的。使用拓扑和能量特性描述了抑制肽和激动剂的化学空间。此外,还使用蛋白质系统结构计算了刺激和抑制蛋白(针对 VEGFR2)的嵌合模型。计算了嵌合蛋白与 VEGFR 的相互作用。进一步使用复流形和高维数据可视化来描述化学空间。结果表明,VEGFR2 与刺激和抑制蛋白共享一个略微相似的化学区域。另一方面,激动剂肽和抑制剂具有不同的化学空间。