• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用预测的蛋白质表面的一级结构预测蛋白质-蛋白质相互作用。

Predicting the protein-protein interactions using primary structures with predicted protein surface.

机构信息

Department of Electrical Engineering, National Cheng Kung University, Tainan, 70101, Taiwan.

出版信息

BMC Bioinformatics. 2010 Jan 18;11 Suppl 1(Suppl 1):S3. doi: 10.1186/1471-2105-11-S1-S3.

DOI:10.1186/1471-2105-11-S1-S3
PMID:20122202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3009501/
Abstract

BACKGROUND

Many biological functions involve various protein-protein interactions (PPIs). Elucidating such interactions is crucial for understanding general principles of cellular systems. Previous studies have shown the potential of predicting PPIs based on only sequence information. Compared to approaches that require other auxiliary information, these sequence-based approaches can be applied to a broader range of applications.

RESULTS

This study presents a novel sequence-based method based on the assumption that protein-protein interactions are more related to amino acids at the surface than those at the core. The present method considers surface information and maintains the advantage of relying on only sequence data by including an accessible surface area (ASA) predictor recently proposed by the authors. This study also reports the experiments conducted to evaluate a) the performance of PPI prediction achieved by including the predicted surface and b) the quality of the predicted surface in comparison with the surface obtained from structures. The experimental results show that surface information helps to predict interacting protein pairs. Furthermore, the prediction performance achieved by using the surface estimated with the ASA predictor is close to that using the surface obtained from protein structures.

CONCLUSION

This work presents a sequence-based method that takes into account surface information for predicting PPIs. The proposed procedure of surface identification improves the prediction performance with an F-measure of 5.1%. The extracted surfaces are also valuable in other biomedical applications that require similar information.

摘要

背景

许多生物功能涉及各种蛋白质-蛋白质相互作用(PPIs)。阐明这些相互作用对于理解细胞系统的一般原理至关重要。先前的研究表明,仅基于序列信息预测 PPIs 具有潜力。与需要其他辅助信息的方法相比,这些基于序列的方法可以应用于更广泛的应用。

结果

本研究提出了一种新的基于序列的方法,该方法基于这样的假设,即蛋白质-蛋白质相互作用与表面上的氨基酸比核心上的氨基酸更相关。本方法考虑了表面信息,并通过包含作者最近提出的可及表面积(ASA)预测器,保持了仅依赖序列数据的优势。本研究还报告了评估以下内容的实验:a)通过包含预测表面来预测 PPI 的性能,以及 b)与从结构中获得的表面相比,预测表面的质量。实验结果表明,表面信息有助于预测相互作用的蛋白质对。此外,使用 ASA 预测器估计的表面进行预测的性能接近使用从蛋白质结构获得的表面进行预测的性能。

结论

本工作提出了一种基于序列的方法,该方法考虑了用于预测 PPIs 的表面信息。表面识别的提议程序可将 F 度量提高到 5.1%,从而提高预测性能。提取的表面在需要类似信息的其他生物医学应用中也很有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/8a84d002184d/1471-2105-11-S1-S3-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/097c91d613ed/1471-2105-11-S1-S3-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/ff0d11c938d8/1471-2105-11-S1-S3-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/804443b46fc1/1471-2105-11-S1-S3-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/083a8153ef3f/1471-2105-11-S1-S3-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/8a84d002184d/1471-2105-11-S1-S3-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/097c91d613ed/1471-2105-11-S1-S3-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/ff0d11c938d8/1471-2105-11-S1-S3-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/804443b46fc1/1471-2105-11-S1-S3-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/083a8153ef3f/1471-2105-11-S1-S3-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fd/3009501/8a84d002184d/1471-2105-11-S1-S3-5.jpg

相似文献

1
Predicting the protein-protein interactions using primary structures with predicted protein surface.利用预测的蛋白质表面的一级结构预测蛋白质-蛋白质相互作用。
BMC Bioinformatics. 2010 Jan 18;11 Suppl 1(Suppl 1):S3. doi: 10.1186/1471-2105-11-S1-S3.
2
Predicting protein-protein interactions in unbalanced data using the primary structure of proteins.利用蛋白质的一级结构预测不平衡数据中的蛋白质-蛋白质相互作用。
BMC Bioinformatics. 2010 Apr 2;11:167. doi: 10.1186/1471-2105-11-167.
3
A discriminative approach for identifying domain-domain interactions from protein-protein interactions.一种从蛋白质相互作用中识别结构域-结构域相互作用的判别方法。
Proteins. 2010 Apr;78(5):1243-53. doi: 10.1002/prot.22643.
4
A Cascade Random Forests Algorithm for Predicting Protein-Protein Interaction Sites.一种用于预测蛋白质-蛋白质相互作用位点的级联随机森林算法。
IEEE Trans Nanobioscience. 2015 Oct;14(7):746-60. doi: 10.1109/TNB.2015.2475359. Epub 2015 Sep 28.
5
Sequence-based prediction of protein-protein interactions using weighted sparse representation model combined with global encoding.基于序列的蛋白质-蛋白质相互作用预测:结合全局编码的加权稀疏表示模型
BMC Bioinformatics. 2016 Apr 26;17(1):184. doi: 10.1186/s12859-016-1035-4.
6
Combining sequence and network information to enhance protein-protein interaction prediction.结合序列和网络信息来增强蛋白质-蛋白质相互作用预测。
BMC Bioinformatics. 2020 Dec 16;21(Suppl 16):537. doi: 10.1186/s12859-020-03896-6.
7
Prediction of protein-protein interactions from amino acid sequences using a novel multi-scale continuous and discontinuous feature set.利用新型多尺度连续和非连续特征集从氨基酸序列预测蛋白质-蛋白质相互作用。
BMC Bioinformatics. 2014;15 Suppl 15(Suppl 15):S9. doi: 10.1186/1471-2105-15-S15-S9. Epub 2014 Dec 3.
8
Predicting protein-protein interactions using high-quality non-interacting pairs.利用高质量的非互作蛋白对预测蛋白质相互作用。
BMC Bioinformatics. 2018 Dec 31;19(Suppl 19):525. doi: 10.1186/s12859-018-2525-3.
9
Predicting gene ontology functions from protein's regional surface structures.从蛋白质的区域表面结构预测基因本体功能。
BMC Bioinformatics. 2007 Dec 11;8:475. doi: 10.1186/1471-2105-8-475.
10
Prediction of protein-protein interactions from protein sequence using local descriptors.利用局部描述符从蛋白质序列预测蛋白质-蛋白质相互作用。
Protein Pept Lett. 2010 Sep;17(9):1085-90. doi: 10.2174/092986610791760306.

引用本文的文献

1
Assigning biological function using hidden signatures in cystine-stabilized peptide sequences.利用胱氨酸稳定肽序列中的隐藏特征赋予生物学功能。
Sci Rep. 2018 Jun 13;8(1):9049. doi: 10.1038/s41598-018-27177-8.
2
SPRINT: ultrafast protein-protein interaction prediction of the entire human interactome.SPRINT:对整个人类相互作用组进行超快速蛋白质-蛋白质相互作用预测。
BMC Bioinformatics. 2017 Nov 15;18(1):485. doi: 10.1186/s12859-017-1871-x.
3
Fundamentals of protein interaction network mapping.蛋白质相互作用网络图谱的基础

本文引用的文献

1
Real value prediction of protein solvent accessibility using enhanced PSSM features.使用增强的位置特异性得分矩阵(PSSM)特征对蛋白质溶剂可及性进行实际值预测。
BMC Bioinformatics. 2008 Dec 12;9 Suppl 12(Suppl 12):S12. doi: 10.1186/1471-2105-9-S12-S12.
2
The Protein Data Bank (PDB), its related services and software tools as key components for in silico guided drug discovery.蛋白质数据库(PDB)及其相关服务和软件工具是计算机辅助药物发现的关键组成部分。
J Med Chem. 2008 Nov 27;51(22):7021-40. doi: 10.1021/jm8005977.
3
The Universal Protein Resource (UniProt) 2009.
Mol Syst Biol. 2015 Dec 17;11(12):848. doi: 10.15252/msb.20156351.
4
Multi-level machine learning prediction of protein-protein interactions in Saccharomyces cerevisiae.酿酒酵母中蛋白质-蛋白质相互作用的多层次机器学习预测
PeerJ. 2015 Jul 2;3:e1041. doi: 10.7717/peerj.1041. eCollection 2015.
5
Improving predictions of protein-protein interfaces by combining amino acid-specific classifiers based on structural and physicochemical descriptors with their weighted neighbor averages.通过将基于结构和物理化学描述符的氨基酸特异性分类器与其加权邻居平均值相结合,提高蛋白质-蛋白质界面的预测。
PLoS One. 2014 Jan 28;9(1):e87107. doi: 10.1371/journal.pone.0087107. eCollection 2014.
6
On protocols and measures for the validation of supervised methods for the inference of biological networks.关于生物网络推断监督方法验证的协议与措施
Front Genet. 2013 Dec 3;4:262. doi: 10.3389/fgene.2013.00262.
7
Combining phylogenetic profiling-based and machine learning-based techniques to predict functional related proteins.结合基于系统发育轮廓和基于机器学习的技术来预测功能相关蛋白。
PLoS One. 2013 Sep 19;8(9):e75940. doi: 10.1371/journal.pone.0075940. eCollection 2013.
8
PPIcons: identification of protein-protein interaction sites in selected organisms.PPIcon:在选定的生物体中鉴定蛋白质-蛋白质相互作用位点。
J Mol Model. 2013 Sep;19(9):4059-70. doi: 10.1007/s00894-013-1886-9. Epub 2013 Jun 2.
9
Protein-protein interaction site predictions with three-dimensional probability distributions of interacting atoms on protein surfaces.利用蛋白质表面相互作用原子的三维概率分布预测蛋白质-蛋白质相互作用位点。
PLoS One. 2012;7(6):e37706. doi: 10.1371/journal.pone.0037706. Epub 2012 Jun 6.
通用蛋白质资源(UniProt)2009 版
Nucleic Acids Res. 2009 Jan;37(Database issue):D169-74. doi: 10.1093/nar/gkn664. Epub 2008 Oct 4.
4
Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks.整合大规模功能基因组数据以剖析酵母调控网络的复杂性。
Nat Genet. 2008 Jul;40(7):854-61. doi: 10.1038/ng.167. Epub 2008 Jun 15.
5
Using support vector machine combined with auto covariance to predict protein-protein interactions from protein sequences.利用支持向量机结合自协方差从蛋白质序列预测蛋白质-蛋白质相互作用。
Nucleic Acids Res. 2008 May;36(9):3025-30. doi: 10.1093/nar/gkn159. Epub 2008 Apr 4.
6
Improving the performance of an SVM-based method for predicting protein-protein interactions.提高一种基于支持向量机的蛋白质-蛋白质相互作用预测方法的性能。
In Silico Biol. 2006;6(6):515-29.
7
Deciphering protein-protein interactions. Part II. Computational methods to predict protein and domain interaction partners.解析蛋白质-蛋白质相互作用。第二部分。预测蛋白质和结构域相互作用伙伴的计算方法。
PLoS Comput Biol. 2007 Apr 27;3(4):e43. doi: 10.1371/journal.pcbi.0030043.
8
Predicting protein-protein interactions based only on sequences information.仅基于序列信息预测蛋白质-蛋白质相互作用。
Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4337-41. doi: 10.1073/pnas.0607879104. Epub 2007 Mar 5.
9
How complete are current yeast and human protein-interaction networks?目前的酵母和人类蛋白质相互作用网络有多完整?
Genome Biol. 2006;7(11):120. doi: 10.1186/gb-2006-7-11-120.
10
The many faces of protein-protein interactions: A compendium of interface geometry.蛋白质-蛋白质相互作用的多样面貌:界面几何学概览。
PLoS Comput Biol. 2006 Sep 29;2(9):e124. doi: 10.1371/journal.pcbi.0020124. Epub 2006 Jul 31.