Nemésio Henrique, Palomares-Jerez Francis, Villalaín José
Universidad Miguel Hernandez, Alicante, Spain.
Biochim Biophys Acta. 2011 Oct;1808(10):2390-402. doi: 10.1016/j.bbamem.2011.06.019. Epub 2011 Jul 13.
We have identified the membranotropic regions of proteins C and E of DENV virus by performing an exhaustive study of membrane rupture induced by two C and E-derived peptide libraries on model membranes having different phospholipid compositions as well as its ability to modulate the DEPE L(β)-L(α) and L(α)-H(II) phospholipid phase transitions. Protein C presents one hydrophobic leakage-prone region coincidental with a proposed membrane interacting domain, whereas protein E presents five membrane-rupture zones coincidental with different significant zones of the protein, i.e., the fusion peptide, a proline-rich sequence, a sequence containing a hydrophobic pocket as well as the stem and transmembrane domains of the protein. The identification of these membrane-active segments supports their role in viral membrane fusion, formation of the replication complex and morphogenesis and therefore attractive targets for development of new anti-viral compounds.
通过对由两个C和E衍生肽库在具有不同磷脂组成的模型膜上诱导的膜破裂进行详尽研究,以及其调节二棕榈酰磷脂酰乙醇胺L(β)-L(α)和L(α)-H(II)磷脂相变的能力,我们确定了登革病毒蛋白C和E的膜otropic区域。蛋白C呈现出一个与提议的膜相互作用结构域重合的疏水性易泄漏区域,而蛋白E呈现出五个与该蛋白不同的重要区域重合膜破裂区域,即融合肽、富含脯氨酸的序列、包含疏水口袋的序列以及该蛋白的茎和跨膜结构域。这些膜活性片段的鉴定支持了它们在病毒膜融合、复制复合体形成和形态发生中的作用,因此是开发新型抗病毒化合物的有吸引力的靶点。