How advancement in biological network analysis methods empowers proteomics

被引:59
作者
Goh, Wilson W. B. [3 ]
Lee, Yie H. [4 ]
Chung, Maxey [5 ,6 ]
Wong, Limsoon [1 ,2 ]
机构
[1] Natl Univ Singapore, Sch Comp, Dept Comp Sci, Singapore 117417, Singapore
[2] Natl Univ Singapore, Dept Pathol, Singapore 117417, Singapore
[3] Univ London Imperial Coll Sci Technol & Med, Dept Comp, London SW7 2AZ, England
[4] Singapore MIT Alliance Res & Technol, Singapore, Singapore
[5] Natl Univ Singapore, Dept Biochem, Singapore 117417, Singapore
[6] Natl Univ Singapore, Dept Biol Sci, Singapore 117417, Singapore
基金
英国惠康基金; 新加坡国家研究基金会;
关键词
Bioinformatics; MS; Network; PROTEIN-PROTEIN INTERACTIONS; GENE-EXPRESSION DATA; MASS-SPECTROMETRY; CAENORHABDITIS-ELEGANS; SEQUENCE-SIGNATURES; MOLECULAR NETWORKS; HIGH-RESOLUTION; ONTOLOGY TERMS; MESSENGER-RNA; IDENTIFICATION;
D O I
10.1002/pmic.201100321
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Proteomics provides important information - that may not be inferable from indirect sources such as RNA or DNA - on key players in biological systems or disease states. However, it suffers from coverage and consistency problems. The advent of network-based analysis methods can help in overcoming these problems but requires careful application and interpretation. This review considers briefly current trends in proteomics technologies and understanding the causes of critical issues that need to be addressed - i.e., incomplete data coverage and inter-sample inconsistency. On the coverage issue, we argue that holistic analysis based on biological networks provides a suitable background on which more robust models and interpretations can be built upon; and we introduce some recently developed approaches. On consistency, group-based approaches based on identified clusters, as well as on properly integrated pathway databases, are particularly useful. Despite that protein interactions and pathway networks are still largely incomplete, given proper quality checks, applications and reasonably sized data sets, they yield valuable insights that greatly complement data generated from quantitative proteomics.
引用
收藏
页码:550 / 563
页数:14
相关论文
共 119 条
[1]
CFinder:: locating cliques and overlapping modules in biological networks [J].
Adamcsek, B ;
Palla, G ;
Farkas, IJ ;
Derényi, I ;
Vicsek, T .
BIOINFORMATICS, 2006, 22 (08) :1021-1023
[2]
Revisiting Date and Party Hubs: Novel Approaches to Role Assignment in Protein Interaction Networks [J].
Agarwal, Sumeet ;
Deane, Charlotte M. ;
Porter, Mason A. ;
Jones, Nick S. .
PLOS COMPUTATIONAL BIOLOGY, 2010, 6 (06) :1-12
[3]
Scale-free networks in cell biology [J].
Albert, R .
JOURNAL OF CELL SCIENCE, 2005, 118 (21) :4947-4957
[4]
Error and attack tolerance of complex networks [J].
Albert, R ;
Jeong, H ;
Barabási, AL .
NATURE, 2000, 406 (6794) :378-382
[5]
Global networks of functional coupling in eukaryotes from comprehensive data integration [J].
Alexeyenko, Andrey ;
Sonnhammer, Erik L. L. .
GENOME RESEARCH, 2009, 19 (06) :1107-1116
[6]
Taking the mystery out of biological networks [J].
Aloy, P ;
Russell, RB .
EMBO REPORTS, 2004, 5 (04) :349-350
[7]
The IntAct molecular interaction database in 2010 [J].
Aranda, B. ;
Achuthan, P. ;
Alam-Faruque, Y. ;
Armean, I. ;
Bridge, A. ;
Derow, C. ;
Feuermann, M. ;
Ghanbarian, A. T. ;
Kerrien, S. ;
Khadake, J. ;
Kerssemakers, J. ;
Leroy, C. ;
Menden, M. ;
Michaut, M. ;
Montecchi-Palazzi, L. ;
Neuhauser, S. N. ;
Orchard, S. ;
Perreau, V. ;
Roechert, B. ;
van Eijk, K. ;
Hermjakob, H. .
NUCLEIC ACIDS RESEARCH, 2010, 38 :D525-D531
[8]
Ashburner M, 2001, GENOME RES, V11, P1425, DOI 10.1101/gr.180801
[9]
An automated method for finding molecular complexes in large protein interaction networks [J].
Bader, GD ;
Hogue, CW .
BMC BIOINFORMATICS, 2003, 4 (1)
[10]
Bell AW, 2009, NAT METHODS, V6, P423, DOI [10.1038/NMETH.1333, 10.1038/nmeth.1333]