Affinity-Based Methods in Drug-Target Discovery

被引:15
|
作者
Rylova, Gabriela [1 ,2 ]
Ozdian, Tomas [1 ,2 ]
Varanasi, Lakshman [1 ,2 ]
Soural, Miroslav [1 ,2 ,3 ]
Hlavac, Jan [1 ,2 ,3 ]
Holub, Dusan [1 ,2 ]
Dzubak, Petr [1 ,2 ]
Hajduch, Marian [1 ,2 ]
机构
[1] Palacky Univ, Expt Med Lab, Inst Mol & Translat Med, Fac Med & Dent, Olomouc 77515, Czech Republic
[2] Univ Hosp Olomouc, Olomouc 77515, Czech Republic
[3] Palacky Univ, Dept Med Chem, Inst Mol & Translat Med, Fac Sci, Olomouc 77146, Czech Republic
关键词
Affinity purification; drug-target discovery; immobilization; mass-spectrometry; probe; quantification; ONE-STEP PURIFICATION; SOLID-PHASE BIOTINYLATION; COMPLEX PROTEIN MIXTURES; SMALL-MOLECULE PROBES; MASS-SPECTROMETRY; LABEL-FREE; CHEMICAL PROTEOMICS; SPACER ARM; ABSOLUTE QUANTIFICATION; QUANTITATIVE-ANALYSIS;
D O I
10.2174/1389450115666141120110323
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Target discovery using the molecular approach, as opposed to the more traditional systems approach requires the study of the cellular or biological process underlying a condition or disease. The approaches that are employed by the "bench" scientist may be genetic, genomic or proteomic and each has its rightful place in the drug-target discovery process. Affinity-based proteomic techniques currently used in drug-discovery draw upon several disciplines, synthetic chemistry, cell-biology, biochemistry and mass spectrometry. An important component of such techniques is the probe that is specifically designed to pick out a protein or set of proteins from amongst the varied thousands in a cell lysate. A second component, that is just as important, is liquid-chromatography tandem massspectrometry (LC-MS/MS). LC-MS/MS and the supporting theoretical framework has come of age and is the tool of choice for protein identification and quantification. These proteomic tools are critical to maintaining the drug-candidate supply, in the larger context of drug discovery.
引用
收藏
页码:60 / 76
页数:17
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