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源自蛋白质组学的肽底物数据的大分子特异性决定因素

Determinants of Macromolecular Specificity from Proteomics-Derived Peptide Substrate Data.

作者信息

Fuchs Julian E, Schilling Oliver, Liedl Klaus R

机构信息

Centre for Molecular Informatics, Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom.

Institute of Molecular Medicine and Cell Research, University of Freiburg, Stefan-Meier- Str. 17, D-79104 Freiburg, Germany.

出版信息

Curr Protein Pept Sci. 2017;18(9):905-913. doi: 10.2174/1389203717666160724211231.

DOI:10.2174/1389203717666160724211231
PMID:27455965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5898033/
Abstract

BACKGROUND

Recent advances in proteomics methodologies allow for high throughput profiling of proteolytic cleavage events. The resulting substrate peptide distributions provide deep insights in the underlying macromolecular recognition events, as determinants of biomolecular specificity identified by proteomics approaches may be compared to structure-based analysis of corresponding protein-protein interfaces.

METHOD

Here, we present an overview of experimental and computational methodologies and tools applied in the area and provide an outlook beyond the protein class of proteases.

RESULTS AND CONCLUSION

We discuss here future potential, synergies and needs of the emerging overlap disciplines of proteomics and structure-based modelling.

摘要

背景

蛋白质组学方法的最新进展使得对蛋白水解切割事件进行高通量分析成为可能。由此产生的底物肽分布为潜在的大分子识别事件提供了深入见解,因为蛋白质组学方法确定的生物分子特异性决定因素可与相应蛋白质-蛋白质界面的基于结构的分析进行比较。

方法

在此,我们概述了该领域应用的实验和计算方法及工具,并展望了蛋白酶蛋白类别之外的情况。

结果与结论

我们在此讨论蛋白质组学和基于结构的建模这两个新兴交叉学科的未来潜力、协同作用及需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/95131ac1eea7/CPPS-18-905_F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/bb90b3075085/CPPS-18-905_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/c935aca6f550/CPPS-18-905_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/95131ac1eea7/CPPS-18-905_F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/bb90b3075085/CPPS-18-905_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/c935aca6f550/CPPS-18-905_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df93/5898033/95131ac1eea7/CPPS-18-905_F3.jpg

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本文引用的文献

1
Efficient Characterization of Protein Cavities within Molecular Simulation Trajectories: trj_cavity.分子模拟轨迹中蛋白质空腔的高效表征:trj_cavity
J Chem Theory Comput. 2014 May 13;10(5):2151-64. doi: 10.1021/ct401098b.
2
Independent Metrics for Protein Backbone and Side-Chain Flexibility: Time Scales and Effects of Ligand Binding.蛋白质主链和侧链柔性的独立指标:时间尺度及配体结合的影响
J Chem Theory Comput. 2015 Mar 10;11(3):851-60. doi: 10.1021/ct500633u. Epub 2015 Feb 24.
3
Dynamics Govern Specificity of a Protein-Protein Interface: Substrate Recognition by Thrombin.
动力学决定蛋白质-蛋白质界面的特异性:凝血酶对底物的识别
PLoS One. 2015 Oct 23;10(10):e0140713. doi: 10.1371/journal.pone.0140713. eCollection 2015.
4
Protein amino-terminal modifications and proteomic approaches for N-terminal profiling.蛋白质氨基末端修饰及氨基末端谱分析的蛋白质组学方法。
Curr Opin Chem Biol. 2015 Feb;24:71-9. doi: 10.1016/j.cbpa.2014.10.026. Epub 2014 Nov 15.
5
Intrinsic flexibility of NLRP pyrin domains is a key factor in their conformational dynamics, fold stability, and dimerization.NLRP 吡啉结构域的内在灵活性是其构象动力学、折叠稳定性和二聚化的关键因素。
Protein Sci. 2015 Feb;24(2):174-81. doi: 10.1002/pro.2601. Epub 2014 Dec 26.
6
Analysis of subpocket selectivity and identification of potent selective inhibitors for matriptase and matriptase-2.分析亚口袋选择性并鉴定针对组织蛋白酶 G 和组织蛋白酶 G2 的强效选择性抑制剂。
J Med Chem. 2014 Dec 11;57(23):10198-204. doi: 10.1021/jm5015633. Epub 2014 Nov 21.
7
Combined experimental and bioinformatics analysis for the prediction and identification of VHR/DUSP3 nuclear targets related to DNA damage and repair.结合实验和生物信息学分析以预测和鉴定与DNA损伤和修复相关的VHR/DUSP3核靶标。
Integr Biol (Camb). 2015 Jan;7(1):73-89. doi: 10.1039/c4ib00186a.
8
Proteome TopFIND 3.0 with TopFINDer and PathFINDer: database and analysis tools for the association of protein termini to pre- and post-translational events.带有TopFINDer和PathFINDer的蛋白质组TopFIND 3.0:用于将蛋白质末端与翻译前和翻译后事件相关联的数据库及分析工具。
Nucleic Acids Res. 2015 Jan;43(Database issue):D290-7. doi: 10.1093/nar/gku1012. Epub 2014 Oct 20.
9
Molecular simulations with solvent competition quantify water displaceability and provide accurate interaction maps of protein binding sites.采用溶剂竞争的分子模拟技术定量评估水的可置换性,并提供蛋白质结合部位的准确相互作用图谱。
J Med Chem. 2014 Oct 23;57(20):8530-9. doi: 10.1021/jm5010418. Epub 2014 Oct 14.
10
Basis for substrate recognition and distinction by matrix metalloproteinases.基质金属蛋白酶对底物的识别与区分基础。
Proc Natl Acad Sci U S A. 2014 Oct 7;111(40):E4148-55. doi: 10.1073/pnas.1406134111. Epub 2014 Sep 22.