thermal shift assays;
isothermal calorimetry;
drug discovery;
PROTEIN STABILITY;
LEAD OPTIMIZATION;
RESIDENCE TIME;
BINDING;
STABILIZATION;
LIGANDS;
D O I:
10.1177/1087057111399573
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The development of new drugs with better pharmacological and safety properties mandates the optimization of several parameters. Today, potency is often used as the sole biochemical parameter to identify and select new molecules. Surprisingly, thermodynamics, which is at the core of any interaction, is rarely used in drug discovery, even though it has been suggested that the selection of scaffolds according to thermodynamic criteria may be a valuable strategy. This poor integration of thermodynamics in drug discovery might be due to difficulties in implementing calorimetry experiments despite recent technological progress in this area. In this report, the authors show that fluorescence-based thermal shift assays could be used as prescreening methods to identify compounds with different thermodynamic profiles. This approach allows a reduction in the number of compounds to be tested in calorimetry experiments, thus favoring greater integration of thermodynamics in drug discovery. (Journal of Biomolecular Screening 2011; 16: 552-556)
机构:
Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USAWyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA
Lo, MC
Aulabaugh, A
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机构:Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA
Aulabaugh, A
Jin, GX
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机构:Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA
Jin, GX
Cowling, R
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机构:Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA
Cowling, R
Bard, J
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机构:Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA
Bard, J
Malamas, M
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机构:Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA
Malamas, M
Ellestad, G
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机构:Wyeth Res, Biophys Enzymol Chem & Screening Sci, Pearl River, NY 10965 USA