GPMelt: A hierarchical Gaussian process framework to explore the dark meltome of thermal proteome profiling experiments.

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2024-09-27 eCollection Date: 2024-09-01 DOI:10.1371/journal.pcbi.1011632
Cecile Le Sueur, Magnus Rattray, Mikhail Savitski
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引用次数: 0

Abstract

Thermal proteome profiling (TPP) is a proteome wide technology that enables unbiased detection of protein drug interactions as well as changes in post-translational state of proteins between different biological conditions. Statistical analysis of temperature range TPP (TPP-TR) datasets relies on comparing protein melting curves, describing the amount of non-denatured proteins as a function of temperature, between different conditions (e.g. presence or absence of a drug). However, state-of-the-art models are restricted to sigmoidal melting behaviours while unconventional melting curves, representing up to 50% of TPP-TR datasets, have recently been shown to carry important biological information. We present a novel statistical framework, based on hierarchical Gaussian process models and named GPMelt, to make TPP-TR datasets analysis unbiased with respect to the melting profiles of proteins. GPMelt scales to multiple conditions, and extension of the model to deeper hierarchies (i.e. with additional sub-levels) allows to deal with complex TPP-TR protocols. Collectively, our statistical framework extends the analysis of TPP-TR datasets for both protein and peptide level melting curves, offering access to thousands of previously excluded melting curves and thus substantially increasing the coverage and the ability of TPP to uncover new biology.

GPMelt:分层高斯过程框架,用于探索热蛋白质组剖析实验的暗熔体组。
热蛋白质组图谱分析(TPP)是一种蛋白质组范围的技术,能够无偏见地检测蛋白质药物相互作用以及不同生物条件下蛋白质翻译后状态的变化。温度范围 TPP(TPP-TR)数据集的统计分析依赖于比较不同条件(如有无药物)下的蛋白质熔解曲线,该曲线描述了非变性蛋白质的数量与温度的函数关系。然而,最先进的模型仅限于西格玛熔解行为,而占 TPP-TR 数据集 50% 的非常规熔解曲线最近被证明携带着重要的生物信息。我们提出了一种基于分层高斯过程模型的新型统计框架,并将其命名为 GPMelt,使 TPP-TR 数据集的分析与蛋白质的熔融曲线无偏见。GPMelt 可扩展到多种条件,并可将模型扩展到更深的层次(即附加子层次),从而处理复杂的 TPP-TR 协议。总之,我们的统计框架扩展了对蛋白质和肽水平熔融曲线的 TPP-TR 数据集的分析,提供了对以前被排除在外的成千上万条熔融曲线的访问,从而大大增加了 TPP 的覆盖范围和发现新生物学的能力。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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