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下一代测序在蛇毒学中的应用:多酶有限消化在蛇毒成分分析中的应用。

Next-Generation Sequencing for Venomics: Application of Multi-Enzymatic Limited Digestion for Inventorying the Snake Venom Arsenal.

机构信息

Laboratory of Mass Spectrometry, MolSys Research Unit, University of Liège, 4000 Liège, Belgium.

GIGA Proteomics Facility, University of Liège, 4000 Liège, Belgium.

出版信息

Toxins (Basel). 2023 May 25;15(6):357. doi: 10.3390/toxins15060357.

Abstract

To improve the characterization of snake venom protein profiles, we report the application of a new generation of proteomic methodology to deeply characterize complex protein mixtures. The new approach, combining a synergic multi-enzymatic and a time-limited digestion (MELD), is a versatile and straightforward protocol previously developed by our group. The higher number of overlapping peptides generated during MELD increases the quality of downstream peptide sequencing and of protein identification. In this context, this work aims at applying the MELD strategy to a venomics purpose for the first time, and especially for the characterization of snake venoms. We used four venoms as the test models for this proof of concept: two Elapidae ( and ) and two Viperidae ( and ). Each venom was reduced and alkylated before being submitted to two different protocols: the classical bottom-up proteomics strategy including a digestion step with trypsin only, or MELD, which combines the activities of trypsin, Glu-C and chymotrypsin with a limited digestion approach. The resulting samples were then injected on an M-Class chromatographic system, and hyphenated to a Q-Exactive Mass Spectrometer. Toxins and protein identification were performed by Peaks Studio X+. The results show that MELD considerably improves the number of sequenced () peptides and identified peptides from protein databases, leading to the unambiguous identification of a greater number of toxins and proteins. For each venom, MELD was successful, not only in terms of the identification of the major toxins (increasing of sequence coverage), but also concerning the less abundant cellular components (identification of new groups of proteins). In light of these results, MELD represents a credible methodology to be applied as the next generation of proteomics approaches dedicated to venomic analysis. It may open new perspectives for the sequencing and inventorying of the venom arsenal and should expand global knowledge about venom composition.

摘要

为了更好地描述蛇毒蛋白图谱,我们报告了一种新一代蛋白质组学方法在深度分析复杂蛋白质混合物中的应用。这种新方法结合了协同的多酶解和限时消化(MELD),是我们小组之前开发的一种多功能且简单的方案。MELD 过程中产生的重叠肽数量增加,提高了下游肽测序和蛋白质鉴定的质量。在这种情况下,本工作首次将 MELD 策略应用于毒液组学,特别是用于蛇毒的特征描述。我们使用四种毒液作为该概念验证的测试模型:两种眼镜蛇科( 和 )和两种蝰蛇科( 和 )。每种毒液在进行两种不同的方案之前都先进行还原和烷基化:经典的自上而下蛋白质组学策略,包括仅用胰蛋白酶进行消化步骤,或 MELD,它结合了胰蛋白酶、Glu-C 和胰凝乳蛋白酶的活性,并采用了有限的消化方法。然后将得到的样品注入 M-Class 色谱系统,并与 Q-Exactive 质谱仪联用。通过 Peaks Studio X+ 进行毒素和蛋白质鉴定。结果表明,MELD 极大地提高了测序肽( )和从蛋白质数据库中鉴定的肽的数量,从而能够明确鉴定出更多的毒素和蛋白质。对于每种毒液,MELD 不仅在主要毒素(增加序列覆盖度)的鉴定方面取得了成功,而且在较不丰富的细胞成分(鉴定新的蛋白质组)方面也取得了成功。鉴于这些结果,MELD 代表了一种可靠的方法,可作为下一代蛋白质组学方法应用于毒液组学分析。它可能为毒液库的测序和编目开辟新的前景,并扩大全球对毒液组成的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fd9/10304959/4bf672f2251d/toxins-15-00357-g001.jpg

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