Dacin,一种从尖锐蝮蛇毒液中提取的金属蛋白酶,能抑制小鼠回肠肌收缩。

Q2 Biochemistry, Genetics and Molecular Biology
Bin Zhou, Gang Liu, Qiyi He, Bo Li, Xiaodong Yu
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引用次数: 0

摘要

背景:小鼠被五步毒蛇(Deinagkistrodon acutus)咬伤,然后中毒。众所周知,蛇毒主要是扰乱受害者的血液稳态。我们偶然发现,尖锐蛇毒可以抑制小鼠回肠收缩张力,因此本研究旨在鉴定蛇毒中抑制小鼠回肠收缩张力的活性成分。结果:从毒D. acutus毒液中分离到抑制小鼠回肠收缩张力的活性成分Dacin,经纯化后蛋白均质,由单肽链组成,SDS-PAGE分析约23 kDa, 22,947。9 .用MALDI-TOF-MS测定Da。用Mascot爆破其PMF的结果表明,Dacin可能是一种蛇毒金属蛋白酶(SVMP),随后的生化和体内实验结果也证实了它是一种SVMP:它能在1 h内裂解牛纤维蛋白原的Aα和Bβ链,而不是Cγ链,并能水解纤维蛋白聚合物;此外,β-巯基乙醇、EDTA和EGTA对其纤维蛋白(基因)裂解活性有较强的抑制作用;并能引起小鼠背皮下出血反应。在离体组织实验中,Dacin对小鼠回肠平滑肌自发收缩张力具有浓度依赖性和时间依赖性的抑制作用,且抑制作用不可逆。结论:本研究首次从急性蝮蛇毒液中分离鉴定出一种不可逆地抑制小鼠回肠自发收缩张力的活性成分(Dacin, SVMP)。这一发现不仅为svmp和毒蛇毒液的毒理学研究提供了新的思路,也为临床医生治疗毒蛇咬伤患者提供了参考。然而,Dacin的抑制分子机制将在未来进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dacin, one metalloproteinase from Deinagkistrodon acutus venom inhibiting contraction of mouse ileum muscle.

Dacin, one metalloproteinase from Deinagkistrodon acutus venom inhibiting contraction of mouse ileum muscle.

Dacin, one metalloproteinase from Deinagkistrodon acutus venom inhibiting contraction of mouse ileum muscle.

Dacin, one metalloproteinase from Deinagkistrodon acutus venom inhibiting contraction of mouse ileum muscle.

Background: Mice were bitten by five-pace vipers (Deinagkistrodon acutus), and then envenomed. It was well-known that the snake venom mainly disturbed the blood homeostasis of the envenomed victims. Ocassionally, we found that the venom of D. acutus could inhibit the contraction tension of mouse ileum, so in this study we aimed to identify the active component inhibiting the contraction tension of mouse ileum in the snake venom.

Results: The active component inhibiting the contraction tension of mouse ileum, designated as Dacin, was isolated from D. acutus venom, purified to protein homogeneity and composed of a single peptide chain, about 23 kDa analyzed by SDS-PAGE, and 22, 947. 9 Da measured by MALDI-TOF-MS. Not only the results of its PMF blasted by Mascot indicated that Dacin may be one snake venom metalloproteinase (SVMP), but also the results of the biochemical and in-vivo assays as follow demonstrated that it was one SVMP: it cleaved Aα and Bβ chains, not Cγ of bovine fibrinogen within 1 h, and also hydrolyzed fibrin polymer; besides its fibrino(geno)lytic activities were strongly inhibited by β- mercaptoethanol, EDTA and EGTA; and it could induce a hemorrhagic reaction under the dorsal skin of mouse. In the isolated tissue assays, Dacin caused the concentration-dependent and time-dependent inhibitory actions on the spontaneous contraction tension of the ileum smooth muscle of mouse, and the inhibitory effects were irreversible.

Conclusions: Taken together, for the first time one active component (Dacin, a SVMP) that irreversibly inhibited the spontaneous contraction tension of mouse ileum has been isolated and identified from D. acutus venom. The findings may provide not only a new insight for toxicological researches on SVMPs and venoms of the vipers, but also a reference for clinicians to treat the snake-bitten victims. However, Dacin's inhibitory molecular mechanism will be further studied in the future.

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来源期刊
BMC Biochemistry
BMC Biochemistry BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
3 months
期刊介绍: BMC Biochemistry is an open access journal publishing original peer-reviewed research articles in all aspects of biochemical processes, including the structure, function and dynamics of metabolic pathways, supramolecular complexes, enzymes, proteins, nucleic acids and small molecular components of organelles, cells and tissues. BMC Biochemistry (ISSN 1471-2091) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record, Thomson Reuters (ISI) and Google Scholar.
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