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中华眼镜蛇(台湾眼镜蛇)毒液中心脏毒素的多样性。

The multiplicity of cardiotoxins from Naja naja atra (Taiwan cobra) venom.

作者信息

Chang L S, Huang H B, Lin S R

机构信息

Institute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung, Taiwan.

出版信息

Toxicon. 2000 Aug;38(8):1065-76. doi: 10.1016/s0041-0101(99)00218-4.

Abstract

Four novel cardiotoxins were isolated from Naja naja atra (Taiwan cobra) venom by successive separation on a SP-Sephadex C-25 column and a reverse phase column. Amino acid sequences of the cardiotoxins were determined by Edman degradation and carboxypeptidase digestion. It shows that these cardiotoxins comprise 60 amino acid residues. Comparative analyses on the amino acid sequences of cardiotoxins from the venoms of N. naja atra and other Naja species indicated that amino acid substitutions of cardiotoxin isoforms frequently occurred at positions 7-11, 27-32 and 45-47. The hypervariable segments encoded by the second and third exon of cardiotoxin genes are located at or near the tips of loop structure of cardiotoxin molecules. These results, together with the suggestions that the residues at the tips of cardiotoxins' loop structure were involved in the manifestation of the biological activities of cardiotoxins, reflect that the preferential mutations may contribute to alterations in the function of cardiotoxin molecules. Analysis on the secondary structure of pre-mRNAs of N. naja atra cardiotoxin 4 gene and N. naja sputatrix cardiotoxin 3 gene has shown that the hypervariable regions of the exon 2 pertain to form intra-exon pairings and are not involved in the formation of intron-exon pairings. Since the pairings of splice sites and gene architecture were supposed to be associated with intron-exon recognition, it is likely that the preferred loci of mutations occurring with the evolution of cardiotoxin genes would not affect the processing of cardiotoxin precursors.

摘要

通过在SP-Sephadex C-25柱和反相柱上连续分离,从眼镜蛇(台湾眼镜蛇)毒液中分离出四种新型心脏毒素。通过埃德曼降解法和羧肽酶消化法测定了心脏毒素的氨基酸序列。结果表明,这些心脏毒素由60个氨基酸残基组成。对眼镜蛇和其他眼镜蛇属物种毒液中心脏毒素氨基酸序列的比较分析表明,心脏毒素亚型的氨基酸取代经常发生在7-11、27-32和45-47位。心脏毒素基因第二和第三外显子编码的高变区位于心脏毒素分子环结构的末端或附近。这些结果,再加上关于心脏毒素环结构末端的残基参与心脏毒素生物活性表现的建议,反映出优先突变可能导致心脏毒素分子功能的改变。对眼镜蛇心脏毒素4基因和菲律宾眼镜蛇心脏毒素3基因前体mRNA二级结构的分析表明,外显子2的高变区形成外显子内配对,不参与内含子-外显子配对的形成。由于剪接位点的配对和基因结构被认为与内含子-外显子识别有关,因此心脏毒素基因进化过程中发生突变的优先位点可能不会影响心脏毒素前体的加工。

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