The Proteomics Big Challenge for Biomarkers and New Drug-Targets Discovery

被引:52
作者
Savino, Rocco [1 ]
Paduano, Sergio [1 ]
Preiano, Mariaimmacolata [1 ]
Terracciano, Rosa [1 ]
机构
[1] Magna Graecia Univ Catanzaro, Lab Mass Spectrometry & Prote, Dept Hlth Sci, I-88100 Catanzaro, Italy
关键词
biomarkers; mass spectrometry; MALDI-TOF; proteomics; bodily fluids; tissues; LASER-DESORPTION/IONIZATION-TIME; FLIGHT MASS-SPECTROMETRY; VIVO PROTEIN BIOTINYLATION; SOLID-PHASE EXTRACTION; SELDI-TOF-MS; NIPPLE ASPIRATE FLUID; QUANTITATIVE PROTEOMICS; SACCHAROMYCES-CEREVISIAE; FUNCTIONAL PROTEOMICS; CLINICAL PROTEOMICS;
D O I
10.3390/ijms131113926
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
In the modern process of drug discovery, clinical, functional and chemical proteomics can converge and integrate synergies. Functional proteomics explores and elucidates the components of pathways and their interactions which, when deregulated, lead to a disease condition. This knowledge allows the design of strategies to target multiple pathways with combinations of pathway-specific drugs, which might increase chances of success and reduce the occurrence of drug resistance. Chemical proteomics, by analyzing the drug interactome, strongly contributes to accelerate the process of new druggable targets discovery. In the research area of clinical proteomics, proteome and peptidome mass spectrometry-profiling of human bodily fluid (plasma, serum, urine and so on), as well as of tissue and of cells, represents a promising tool for novel biomarker and eventually new druggable targets discovery. In the present review we provide a survey of current strategies of functional, chemical and clinical proteomics. Major issues will be presented for proteomic technologies used for the discovery of biomarkers for early disease diagnosis and identification of new drug targets.
引用
收藏
页码:13926 / 13948
页数:23
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