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A Multiomics Approach Unravels New Toxins With Possible In Silico Antimicrobial, Antiviral, and Antitumoral Activities in the Venom of Acanthoscurria rondoniae

机译:多孔方法方法在硅藻土的毒液中的硅抗菌,抗病毒和抗肿瘤活动中可以在可能的毒性抗菌和抗肿瘤活动中解开新的毒素

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摘要

The Araneae order is considered one of the most successful groups among venomous animals in the world. An important factor for this success is the production of venoms, a refined biological fluid rich in proteins, short peptides and cysteine-rich peptides (CRPs). These toxins may present pharmacologically relevant biological actions, as antimicrobial, antiviral and anticancer activities, for instance. Therefore, there is an increasing interest in the exploration of venom toxins for therapeutic reasons, such as drug development. However, the process of peptide sequencing and mainly the evaluation of potential biological activities of these peptides are laborious, considering the low yield of venom extraction and the high variability of toxins present in spider venoms. Here we show a robust methodology for identification, sequencing, and initial screening of potential bioactive peptides found in the venom of Acanthoscurria rondoniae. This methodology consists in a multiomics approach involving proteomics, peptidomics and transcriptomics analyses allied to in silico predictions of antibacterial, antifungal, antiviral, and anticancer activities. Through the application of this strategy, a total of 92,889 venom gland transcripts were assembled and 84 novel toxins were identified at the protein level, including seven short peptides and 10 fully sequenced CRPs (belonging to seven toxin families). In silico analysis suggests that seven CRPs families may have potential antimicrobial or antiviral activities, while two CRPs and four short peptides are potentially anticancer. Taken together, our results demonstrate an effective multiomics strategy for the discovery of new toxins and in silico screening of potential bioactivities. This strategy may be useful in toxin discovery, as well as in the screening of possible activities for the vast diversity of molecules produced by venomous animals.
机译:该蜘蛛为了被认为是世界上有毒动物中最成功的团体之一。这一成功的一个重要因素是生产毒液,经精制生物液体含有丰富的蛋白质,短肽和富含半胱氨酸的肽(协调研究项目)。这些毒素可能会出现药理学相关的生物作用,如抗菌,抗病毒和抗癌活性,例如。因此,在蛇毒毒素治疗的原因,如药物开发勘探越来越感兴趣。然而,肽测序的过程以及这些肽的潜在生物活性主要是评价是费力,考虑毒液提取的低收率和存在于蜘蛛毒液毒素高可变性。在这里,我们显示了鉴定,测序,并在Acanthoscurria rondoniae的毒液中发现潜在的生物活性肽的初步筛选一个完善的方法。该方法包括在multiomics办法,让蛋白质组学,peptidomics和转录组分析中的抗菌,抗真菌,抗病毒和抗癌活动硅片预测结盟。通过这种策略的应用,共92889毒腺转录组装并鉴定在蛋白水平上84种新颖毒素,包括7种短肽和10组完全测序的CRP(属于7毒素家族)。在硅片分析表明有七个家庭的CRP可能具有潜在的抗菌或抗病毒活性,另外两个协调研究项目和四个短肽是潜在的抗癌。总之,我们的结果表明,为新毒素的发现和在硅片潜在的生物活性筛选的有效multiomics策略。这种策略可以在可能进行的活动的筛选由有毒动物产生的分子的巨大多样性毒素发现有用的,以及。

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