Romagnoli Silvia, Fogolari Federico, Catalano Maddalena, Zetta Lucia, Schaller Gerhard, Urech Konrad, Giannattasio Matteo, Ragona Laura, Molinari Henriette
Dipartimento Scientifico e Tecnologico, Università degli Studi di Verona, Strada le Grazie 15, 37134 Verona, Italy.
Biochemistry. 2003 Nov 4;42(43):12503-10. doi: 10.1021/bi034762t.
The high resolution three-dimensional structure of the newly discovered plant viscotoxin C1, from the Asiatic Viscum album ssp. Coloratum ohwi, has been determined in solution by (1)H NMR spectroscopy at pH 3.6 and 285 K. The viscotoxin C1-fold, consisting of a helix-turn-helix motif and a short stretch of an antiparralel beta-sheet is very similar to that found for the highly similar viscotoxins A2 and A3 and for other related thionins. Different functional properties of members of the thionin family are discussed here in light of the structural and electrostatic properties. Among the very homologous family of alpha- and beta-thionins, known for their antimicrobial activity, the viscotoxin subfamily differs from the other members because of its high toxicity against tumoral cells. Key residues for the modulation of viscotoxin cytotoxicity have been identified on the basis of sequence and structural alignment.
通过在pH 3.6和285 K条件下的¹H NMR光谱法,已在溶液中确定了新发现的来自日本桑寄生(Viscum album ssp. Coloratum ohwi)的植物毒蛋白C1的高分辨率三维结构。毒蛋白C1的折叠结构由一个螺旋-转角-螺旋基序和一小段反平行β-折叠组成,与高度相似的毒蛋白A2和A3以及其他相关硫堇蛋白的折叠结构非常相似。本文根据结构和静电性质讨论了硫堇蛋白家族成员的不同功能特性。在以抗菌活性闻名的α-和β-硫堇蛋白这一同源度很高的家族中,毒蛋白亚家族因其对肿瘤细胞的高毒性而与其他成员不同。已根据序列和结构比对确定了调节毒蛋白细胞毒性的关键残基。