Dipartimento di Scienze della Vita, Seconda Università di Napoli, I-81100 Caserta, Italy.
Int J Biol Macromol. 2009 Nov 1;45(4):407-13. doi: 10.1016/j.ijbiomac.2009.06.015. Epub 2009 Jul 8.
Volkensin, isolated from Adenia volkensii, is one of the most toxic type 2 ribosome-inactivating protein (RIP), exerting its biological function by inhibiting protein synthesis. Despite the high sequence identity with type 2 RIPs, including ricin, volkensin shows interesting peculiar properties. In this work a computational model building of volkensin was performed. The volkensin electrostatic potential charge distribution, the hydrophobic profile and the surface topology analyses were also carried out to aid the understanding of structure-function relationships of this potent toxin. Volkensin surface topology was probed by applying a limited proteolysis approach with the aim to gain insights into volkensin conformational features.
沃尔肯辛(Volkensin)是从阿德尼亚沃尔肯斯氏菌(Adenia volkensii)中分离出来的一种最毒的 2 型核糖体失活蛋白(RIP),通过抑制蛋白质合成来发挥其生物学功能。尽管与包括蓖麻毒素在内的 2 型 RIP 具有很高的序列同一性,但沃尔肯辛表现出了有趣的特殊性质。在这项工作中,对沃尔肯辛进行了计算模型构建。还进行了沃尔肯辛静电势电荷分布、疏水性分布和表面拓扑分析,以帮助理解这种强效毒素的结构-功能关系。通过应用有限的蛋白水解方法来探测沃尔肯辛的表面拓扑结构,目的是深入了解沃尔肯辛的构象特征。