학술논문

The Future of Large-Scale Collaborative Proteomics
Document Type
Periodical
Source
Proceedings of the IEEE Proc. IEEE Proceedings of the IEEE. 96(8):1292-1309 Aug, 2008
Subject
General Topics for Engineers
Engineering Profession
Aerospace
Bioengineering
Components, Circuits, Devices and Systems
Computing and Processing
Engineered Materials, Dielectrics and Plasmas
Fields, Waves and Electromagnetics
Geoscience
Nuclear Engineering
Robotics and Control Systems
Signal Processing and Analysis
Transportation
Power, Energy and Industry Applications
Communication, Networking and Broadcast Technologies
Photonics and Electrooptics
Large-scale systems
Collaboration
Proteomics
Biomarkers
Laboratories
Collaborative work
Proteins
Diseases
Acceleration
Drugs
Biomarker discovery
databases
high-performance computing
image analysis
image registration
liquid chromatography
mass spectrometry
microarray normalization
proteomics
systems biology
two-dimensional gel electrophoresis
Language
ISSN
0018-9219
1558-2256
Abstract
The postgenomics era has witnessed a rapid change in biological methods for knowledge elucidation and pharmacological approaches to biomarker discovery. Differential expression of proteins in health and disease holds the key to early diagnosis and accelerated drug discovery. This approach, however, has also brought an explosion of data complexity not mirrored by existing progress in proteome informatics. It has become apparent that the task is greater than that can be tackled by individual laboratories alone and large-scale open collaborations of the new Human Proteome Organization (HUPO) have highlighted major challenges concerning the integration and cross-validation of results across different laboratories. This paper describes the state-of-the-art proteomics workflows (two-dimensional gel electrophoresis, liquid chromatography, and mass spectrometry) and their utilization by the participants of the HUPO initiatives towards comprehensive mapping of the brain, liver, and plasma proteomes. Particular emphasis is given to the limitations of the underlying data analysis techniques for large-scale collaborative proteomics. Emerging paradigms including statistical data normalization, direct image registration, spectral libraries, and high-throughput computation with Web-based bioinformatics services are discussed. It is envisaged that these methods will provide the basis for breaking the bottleneck of large-scale automated proteome mapping and biomarker discovery.