Summary
As the field of clinical proteomics progresses, discovery of disease biomarkers becomes paramount. However, the immediate challenges are to establish standard operating procedures for both clinical specimen handling and reduction of sample complexity and to increase the ability to detect proteins and peptides present in low amounts. The traditional concept of a disease biomarker is shifting toward a new paradigm, namely, that an ensemble of proteins or peptides would be more efficient than a single protein/peptide in the diagnosis of disease. Because clinical proteomics usually requires easy access to well-defined fresh clinical specimens (including morphologically consistent tissue and properly pretreated body fluids of sufficient quantity), biorepository systems need to be established. Here, we address these questions and emphasize the necessity of developing various microdissection techniques for tissue specimens, multidimensional fractionation for body fluids, and other related techniques (including bioinformatics), tools which could become integral parts of clinical proteomics for disease biomarker discovery.
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Abbreviations
- CSF:
-
Cerebrospinal Fluid
- SILAC:
-
Stable Isotope Labeling with Amino acids in Cell culture
- FFE:
-
Free Flow Electrophoresis
- IMAC:
-
Immobilized Metal Affinity Chromatography
- 2DE:
-
2-dimensional Gel electrophoresis
- CBB:
-
Coomassie Brilliant Blue
- SELDI:
-
Surface-Enhanced Laser Desorption/Ionization
- MALDI:
-
Matrix-Assisted laser desorption/ionization
- MDLC:
-
Multi-dimensional Liquid Chromatography
- LC:
-
Liquid Chromatography
- TOF:
-
Time-of-Flight
- CID:
-
Collision-induced dissociation
- ETD:
-
Electron Transfer Dissociation
- LIT:
-
Linear Ion-Trap
- FT:
-
Fourier-Transform
- Q:
-
Quadrupole
- ELISA:
-
Enzyme-Linked Immunosorbent Assay
- SISCAPA:
-
Stable Isotope Standards with Capture by Anti-Peptide Antibody
- AQUA:
-
Absolute Quantitative Analysis. Commercial brands are also shown
- MARS:
-
Multiple Affinity Removal System (Agilent Palo Alto CA USA)
- Enchant™:
-
Enchant™ Multi-protein Affinity Separation Kit (Pall Life Sciences Ann Arbor MI USA)
- Gradiflow™:
-
Gradiflow™ Separation (Life Bioprocess Frenchs Forest, Australia)
- FFE™:
-
BD Free Flow Electrophoresis System (BD Diagnostics, Martinsried/Planegg, Germany)
- Zoom® :
-
Zoom® Benchtop Proteomics System (Invitrogen Corporation, Carlsbad, CA, USA)
- Rotofor:
-
Bio-Rad Rotofor® Prep IEF Ccll (Bio-Rad, Hercules, CA, USA)
- PF2D:
-
ProteomeLab™ PF2D Protein Fractionation System (Beckman Coulter, Inc., Fullerton, CA, USA)
- DIGE:
-
Ettan™ DIGE System (GE Healthcare Bio-Sciences AB, Uppsala, Sweden)
- Deep Purple™:
-
Deep Purple™ Total Pprotein Stain (GE Healthcare Bio-Sciences AB, Uppsala, Sweden)
- ICAT™:
-
Isotope-coded affinity tags (Applied Biosystems, Foster City, CA, USA)
- iTRAQ™:
-
iTRAQ™ Reagents (Applied Biosystems, Foster City, CA, USA)
- Q-TRAP™:
-
(Applied Biosystems, Foster City, CA, USA)
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Acknowledgments
This study was supported by a grant from the Korea Health 21 R&D project, Ministry of Health & Welfare, Republic of Korea (A030003 to YKP).
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Paik, YK., Kim, H., Lee, EY., Kwon, MS., Cho, S.Y. (2008). Overview and Introduction to Clinical Proteomics. In: Vlahou, A. (eds) Clinical Proteomics. Methods in Molecular Biology™, vol 428. Humana Press. https://doi.org/10.1007/978-1-59745-117-8_1
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