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曲霉属核糖体毒素氨基末端β-发夹在与膜相互作用及非特异性核糖核酸酶活性中的作用。

Involvement of the amino-terminal beta-hairpin of the Aspergillus ribotoxins on the interaction with membranes and nonspecific ribonuclease activity.

作者信息

García-Ortega L, Lacadena J, Mancheño J M, Oñaderra M, Kao R, Davies J, Olmo N, Gavilanes J G

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Química, Universidad Complutense, 28040 Madrid, Spain.

出版信息

Protein Sci. 2001 Aug;10(8):1658-68. doi: 10.1110/ps.9601.

Abstract

Ribotoxins are a family of potent cytotoxic proteins from Aspergillus whose members display a high sequence identity (85% for about 150 amino acid residues). The three-dimensional structures of two of these proteins, alpha-sarcin and restrictocin, are known. They interact with phospholipid bilayers, according to their ability to enter cells, and cleave a specific phosphodiester bond in the large subunit of ribosome thus inhibiting protein biosynthesis. Two nonconservative sequence changes between these proteins are located at the amino-terminal beta-hairpin of alpha-sarcin, a characteristic structure that is absent in other nontoxic structurally related microbial RNases. These two residues of alpha-sarcin, Lys 11 and Thr 20, have been substituted with the equivalent amino acids in restrictocin. The single mutants (K11L and T20D) and the corresponding K11L/T20D double mutant have been produced in Escherichia coli and purified to homogeneity. The spectroscopic characterization of the purified proteins reveals that the overall native structure is preserved. The ribonuclease and lipid-perturbing activities of the three mutants and restrictocin have been evaluated and compared with those of alpha-sarcin. These proteins exhibit the same ability to specifically inactivate ribosomes, although they show different activity against nonspecific substrate analogs such as poly(A). The mutant variant K11L and restrictocin display a lower phospholipid-interacting ability correlated with a decreased cytotoxicity. The results obtained are interpreted in terms of the involvement of the amino-terminal beta-hairpin in the interaction with both membranes and polyadenylic acid.

摘要

核糖体毒素是一类来自曲霉菌的强效细胞毒性蛋白,其成员具有高度的序列同一性(约150个氨基酸残基的序列同一性为85%)。已知其中两种蛋白α-肌动蛋白和限制酶的三维结构。它们根据进入细胞的能力与磷脂双层相互作用,并切割核糖体大亚基中的特定磷酸二酯键,从而抑制蛋白质生物合成。这两种蛋白之间的两个非保守序列变化位于α-肌动蛋白的氨基末端β-发夹结构处,这是一种在其他无毒的结构相关微生物核糖核酸酶中不存在的特征性结构。α-肌动蛋白的这两个残基,即赖氨酸11和苏氨酸20,已被限制酶中的等效氨基酸取代。单一突变体(K11L和T20D)以及相应的K11L/T20D双突变体已在大肠杆菌中产生并纯化至同质。纯化蛋白的光谱表征表明其整体天然结构得以保留。已对这三种突变体和限制酶的核糖核酸酶及脂质干扰活性进行了评估,并与α-肌动蛋白的活性进行了比较。这些蛋白表现出相同的特异性使核糖体失活的能力,尽管它们对非特异性底物类似物如聚腺苷酸表现出不同的活性。突变体变体K11L和限制酶表现出较低的磷脂相互作用能力,这与细胞毒性降低相关。所得结果从氨基末端β-发夹结构在与膜和聚腺苷酸相互作用中的参与角度进行了解释。

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