Effect of training datasets on support vector machine prediction of protein-protein interactions

被引:62
作者
Lo, SL
Cai, CZ
Chen, YZ
Chung, MCM
机构
[1] Natl Univ Singapore, Dept Biochem, Singapore 117597, Singapore
[2] Natl Univ Singapore, Bioproc Technol Inst, Singapore 117597, Singapore
[3] Natl Univ Singapore, Dept Computat Sci, Singapore 117597, Singapore
[4] Natl Univ Singapore, Dept Biochem, Singapore 117597, Singapore
关键词
database of interacting proteins; protein function prediction; protein-protein interaction; shuffled sequence; support vector machine; SVMlight;
D O I
10.1002/pmic.200401118
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Knowledge of protein-protein interaction is useful for elucidating protein function via the concept of 'guilt-by-association'. A statistical learning method, Support Vector Machine (SVM), has recently been explored for the prediction of protein-protein interactions using artificial shuffled sequences as hypothetical noninteracting proteins and it has shown promising results (Bock, J. R., Gough, D. A., Bioinformatics 2001, 17, 455-460). It remains unclear however, how the prediction accuracy is affected if real protein sequences are used to represent noninteracting proteins. In this work, this effect is assessed by comparison of the results derived from the use of real protein sequences with that derived from the use of shuffled sequences. The real protein sequences of hypothetical noninteracting proteins are generated from an exclusion analysis in combination with subcellular localization information of interacting proteins found in the Database of Interacting Proteins. Prediction accuracy using real protein sequences is 76.9% compared to 94.1% using artificial shuffled sequences. The discrepancy likely arises from the expected higher level of difficulty for separating two sets of real protein sequences than that for separating a set of real protein sequences from a set of artificial sequences. The use of real protein sequences for training a SVM classification system is expected to give better prediction results in practical cases. This is tested by using both SVM systems for predicting putative protein partners of a set of thioredoxin related proteins. The prediction results are consistent with observations, suggesting that real sequence is more practically useful in development of SVM classification system for facilitating protein-protein interaction prediction.
引用
收藏
页码:876 / 884
页数:9
相关论文
共 45 条
  • [11] Czerminski R, 2001, QUANT STRUCT-ACT REL, V20, P227, DOI 10.1002/1521-3838(200110)20:3<227::AID-QSAR227>3.0.CO
  • [12] 2-Y
  • [13] Conservation of gene order: a fingerprint of proteins that physically interact
    Dandekar, T
    Snel, B
    Huynen, M
    Bork, P
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (09) : 324 - 328
  • [14] DEANE CM, 2002, MOL CELLULAR PROTEOM, P349
  • [15] Multi-class protein fold recognition using support vector machines and neural networks
    Ding, CHQ
    Dubchak, I
    [J]. BIOINFORMATICS, 2001, 17 (04) : 349 - 358
  • [16] Redox regulation and signaling lipids in mitochondrial apoptosis
    Fernández-Checa, JC
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (03) : 471 - 479
  • [17] A NOVEL GENETIC SYSTEM TO DETECT PROTEIN PROTEIN INTERACTIONS
    FIELDS, S
    SONG, OK
    [J]. NATURE, 1989, 340 (6230) : 245 - 246
  • [18] Functional organization of the yeast proteome by systematic analysis of protein complexes
    Gavin, AC
    Bösche, M
    Krause, R
    Grandi, P
    Marzioch, M
    Bauer, A
    Schultz, J
    Rick, JM
    Michon, AM
    Cruciat, CM
    Remor, M
    Höfert, C
    Schelder, M
    Brajenovic, M
    Ruffner, H
    Merino, A
    Klein, K
    Hudak, M
    Dickson, D
    Rudi, T
    Gnau, V
    Bauch, A
    Bastuck, S
    Huhse, B
    Leutwein, C
    Heurtier, MA
    Copley, RR
    Edelmann, A
    Querfurth, E
    Rybin, V
    Drewes, G
    Raida, M
    Bouwmeester, T
    Bork, P
    Seraphin, B
    Kuster, B
    Neubauer, G
    Superti-Furga, G
    [J]. NATURE, 2002, 415 (6868) : 141 - 147
  • [19] A protein interaction map of Drosophila melanogaster
    Giot, L
    Bader, JS
    Brouwer, C
    Chaudhuri, A
    Kuang, B
    Li, Y
    Hao, YL
    Ooi, CE
    Godwin, B
    Vitols, E
    Vijayadamodar, G
    Pochart, P
    Machineni, H
    Welsh, M
    Kong, Y
    Zerhusen, B
    Malcolm, R
    Varrone, Z
    Collis, A
    Minto, M
    Burgess, S
    McDaniel, L
    Stimpson, E
    Spriggs, F
    Williams, J
    Neurath, K
    Ioime, N
    Agee, M
    Voss, E
    Furtak, K
    Renzulli, R
    Aanensen, N
    Carrolla, S
    Bickelhaupt, E
    Lazovatsky, Y
    DaSilva, A
    Zhong, J
    Stanyon, CA
    Finley, RL
    White, KP
    Braverman, M
    Jarvie, T
    Gold, S
    Leach, M
    Knight, J
    Shimkets, RA
    McKenna, MP
    Chant, J
    Rothberg, JM
    [J]. SCIENCE, 2003, 302 (5651) : 1727 - 1736
  • [20] Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometry
    Ho, Y
    Gruhler, A
    Heilbut, A
    Bader, GD
    Moore, L
    Adams, SL
    Millar, A
    Taylor, P
    Bennett, K
    Boutilier, K
    Yang, LY
    Wolting, C
    Donaldson, I
    Schandorff, S
    Shewnarane, J
    Vo, M
    Taggart, J
    Goudreault, M
    Muskat, B
    Alfarano, C
    Dewar, D
    Lin, Z
    Michalickova, K
    Willems, AR
    Sassi, H
    Nielsen, PA
    Rasmussen, KJ
    Andersen, JR
    Johansen, LE
    Hansen, LH
    Jespersen, H
    Podtelejnikov, A
    Nielsen, E
    Crawford, J
    Poulsen, V
    Sorensen, BD
    Matthiesen, J
    Hendrickson, RC
    Gleeson, F
    Pawson, T
    Moran, MF
    Durocher, D
    Mann, M
    Hogue, CWV
    Figeys, D
    Tyers, M
    [J]. NATURE, 2002, 415 (6868) : 180 - 183