Prediction of change in protein unfolding rates upon point mutations in two state proteins

被引:4
|
作者
Chaudhary, Priyashree [1 ]
Naganathan, Athi N. [1 ]
Gromiha, M. Michael [1 ]
机构
[1] Indian Inst Technol, Bhupat &Jyoti Mehta Sch Biosci, Dept Biotechnol, Madras 600036, Tamil Nadu, India
来源
关键词
Two-state proteins; Unfolding rates; Point mutations; Multiple regression technique; Machine teaming; Amino acid properties; FOLDING RATE PREDICTION; AMINO-ACID-SEQUENCE; 2-STATE PROTEINS; STRUCTURAL CLASS; CONTACT ORDER; DETERMINANTS; PLACEMENT; STABILITY; DATABASE; KINETICS;
D O I
10.1016/j.bbapap.2016.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies on protein unfolding rates are limited and challenging due to the complexity of unfolding mechanism and the larger dynamic range of the experimental data. Though attempts have been made to predict unfolding rates using protein sequence-structure information there is no available method for predicting the unfolding rates of proteins upon specific point mutations. In this work, we have systematically analyzed a set of 790 single mutants and developed a robust method for predicting protein unfolding rates upon mutations (Delta lnk(u)) in two-state proteins by combining amino acid properties and knowledge-based classification of mutants with multiple linear regression technique. We obtain a mean absolute error (MAE) of 0.79/s and a Pearson correlation coefficient (PCC) of 0.71 between predicted unfolding rates and experimental observations using jack-knife test We have developed a web server for predicting protein unfolding rates upon mutation and it is freely available at https://www.iitm.ac.in/bioinfo/proteinunfolding/unfoldingrace.html. Prominent features that determine unfolding kinetics as well as plausible reasons for the observed outliers are also discussed. (C) 2016 Elsevier B.V. All rights reserved.
引用
下载
收藏
页码:1104 / 1109
页数:6
相关论文
共 50 条
  • [11] A three-state prediction of single point mutations on protein stability changes
    Emidio Capriotti
    Piero Fariselli
    Ivan Rossi
    Rita Casadio
    BMC Bioinformatics, 9
  • [12] Molecular Determinants of Temperature Dependence of Protein Volume Change upon Unfolding
    Chen, Calvin R.
    Makhatadze, George I.
    JOURNAL OF PHYSICAL CHEMISTRY B, 2017, 121 (35): : 8300 - 8310
  • [13] MAESTRO - multi agent stability prediction upon point mutations
    Josef Laimer
    Heidi Hofer
    Marko Fritz
    Stefan Wegenkittl
    Peter Lackner
    BMC Bioinformatics, 16
  • [14] MAESTRO - multi agent stability prediction upon point mutations
    Laimer, Josef
    Hofer, Heidi
    Fritz, Marko
    Wegenkittl, Stefan
    Lackner, Peter
    BMC BIOINFORMATICS, 2015, 16
  • [15] Point mutations in membrane proteins reshape energy landscape and populate different unfolding pathways
    Sapra, K. Tanuj
    Balasubramanian, G. Prakash
    Labudde, Dirk
    Bowie, James U.
    Muller, Daniel J.
    JOURNAL OF MOLECULAR BIOLOGY, 2008, 376 (04) : 1076 - 1090
  • [16] A method for efficient calculation of thermal stability of proteins upon point mutations
    Wang, Bo
    Qi, Yifei
    Gao, Ya
    Zhang, John Z. H.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2020, 22 (16) : 8461 - 8466
  • [17] Wavelet change-point prediction of transmembrane proteins
    Lio, P
    Vannucci, M
    BIOINFORMATICS, 2000, 16 (04) : 376 - 382
  • [18] Prediction in changes of protein thermodynamic stability upon single mutations
    Demenkov, P. S.
    Ivanisenko, V. A.
    PROCEEDINGS OF THE FIFTH INTERNATIONAL CONFERENCE ON BIOINFORMATICS OF GENOME REGULATION AND STRUCTURE, VOL 1, 2006, : 256 - +
  • [19] Long-Range Contacts in Unfolding of Two-State Proteins
    Samuel, Selvaraj
    Balasubramanian, Harihar
    PROTEIN AND PEPTIDE LETTERS, 2017, 24 (03): : 206 - 214
  • [20] Theoretical Prediction of Thermal-Stability Changes upon Mutations of a Protein
    Murakami, Shota
    Oshima, Hiraku
    Hayashi, Tomohiko
    Kinoshita, Masahiro
    BIOPHYSICAL JOURNAL, 2015, 108 (02) : 522A - 522A