孤翅小蜂腹侧凸斑蜂毒液中新的神经保护肽。

IF 1.8 3区 医学 Q4 TOXICOLOGY
Carlos Alberto-Silva, Fernanda Calheta Vieira Portaro, Roberto Tadashi Kodama, Halyne Queiroz Pantaleão, Marisa Rangel, Ken-Ichi Nihei, Katsuhiro Konno
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引用次数: 4

摘要

背景:独居黄蜂的毒液可能是神经活性物质的丰富来源,因为它们的毒液被用来麻痹猎物。我们一直在探索孤独黄蜂毒液的生物活性成分,在本研究中,通过LC-MS综合分析了孤独黄蜂毒液的成分谱。合成了两种多肽,并对其神经保护作用进行了评价。方法:采用反相高效液相色谱联用ESI-MS进行液相色谱-质谱分析。TIC进行在线质量指纹识别,数据依赖串联质谱法获得MS/MS谱。通过MALDI-TOF/TOF质谱分析确定了两种主要肽组分的序列,并通过固相合成进行了证实。利用合成肽对其生物活性进行了评价。使用H2O2作为氧化应激诱导剂对两种肽进行细胞完整性测试和神经保护分析。结果:在线海量指纹图谱显示,该毒液含有123个成分,MS/MS分析得到33个肽成分全序列。α-侧旋啶(DYVTVKGFSPLR)和β-侧旋啶(DYVTVKGFSPLRKA)两种主要肽与缓激肽c端具有同源性。尽管如此,这两种肽都不表现为ACE的底物或抑制剂,表明它们不与ACE金属肽酶相互作用。在进一步的研究中,通过完整性和代谢细胞测定,β-侧方啶而非α -侧方啶对PC12细胞氧化应激诱导的神经毒性具有保护作用。有趣的是,与α-scoliidine相比,β-scoliidine在c端有KA二肽的延伸。结论:用LC-MS和MS/MS综合分析显示了该毒液的成分特征。β-scoliidine显示出有效的细胞保护作用,可能是由于观察到细胞数量的增加。这是首次报道单独的黄蜂毒液肽显示神经保护活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel neuroprotective peptides in the venom of the solitary scoliid wasp <i>Scolia decorata ventralis</i>.

Novel neuroprotective peptides in the venom of the solitary scoliid wasp <i>Scolia decorata ventralis</i>.

Novel neuroprotective peptides in the venom of the solitary scoliid wasp <i>Scolia decorata ventralis</i>.

Novel neuroprotective peptides in the venom of the solitary scoliid wasp Scolia decorata ventralis.

Background: Solitary wasp venoms may be a rich source of neuroactive substances, since their venoms are used for paralyzing preys. We have been exploring bioactive constituents of solitary wasp venoms and, in this study, the component profile of the venom from a solitary scoliid wasp, Scolia decorata ventralis, was investigated through a comprehensive analysis using LC-MS. Two peptides were synthesized, and their neuroprotective properties were evaluated.

Methods: A reverse-phase HPLC connected to ESI-MS was used for LC-MS analyses. Online mass fingerprinting was performed from TIC, and data-dependent tandem mass spectrometry gave the MS/MS spectra. The sequences of two major peptide components were determined by MALDI-TOF/TOF MS analysis, confirmed by solid phase synthesis. Using the synthetic peptides, biological activities were assessed. Cell integrity tests and neuroprotection analyzes using H2O2 as an oxidative stress inducer were performed for both peptides.

Results: Online mass fingerprinting revealed that the venom contains 123 components, and the MS/MS analysis resulted in 33 full sequences of peptide components. The two main peptides, α-scoliidine (DYVTVKGFSPLR) and β-scoliidine (DYVTVKGFSPLRKA), present homology with the bradykinin C-terminal. Despite this, both peptides did not behave as substrates or inhibitors of ACE, indicating that they do not interact with this metallopeptidase. In further studies, β-scoliidine, but not α -scoliidine, showed protective effects against oxidative stress-induced neurotoxicity in PC12 cells through integrity and metabolism cell assays. Interestingly, β-scoliidine has the extension of the KA dipeptide at the C-terminal in comparison with α-scoliidine.

Conclusion: Comprehensive LC-MS and MS/MS analyses from the Scolia decorata ventralis venom displayed the component profile of this venom. β-scoliidine showed an effective cytoprotective effect, probably due to the observed increase in the number of cells. This is the first report of solitary wasp venom peptides showing neuroprotective activity.

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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Journal of Venomous Animals and Toxins including Tropical Diseases (JVATiTD) is a non-commercial academic open access publication dedicated to research on all aspects of toxinology, venomous animals and tropical diseases. Its interdisciplinary content includes original scientific articles covering research on toxins derived from animals, plants and microorganisms. Topics of interest include, but are not limited to:systematics and morphology of venomous animals;physiology, biochemistry, pharmacology and immunology of toxins;epidemiology, clinical aspects and treatment of envenoming by different animals, plants and microorganisms;development and evaluation of antivenoms and toxin-derivative products;epidemiology, clinical aspects and treatment of tropical diseases (caused by virus, bacteria, algae, fungi and parasites) including the neglected tropical diseases (NTDs) defined by the World Health Organization.
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