While saturation transfer difference (STD) is a widely used NMR method for ligand screening, the selection of specific binders requires the validation of the hits through competition experiments or orthogonal biophysical techniques. We show here that the quantitative STD analysis is a reliable and robust approach to discriminate between specific and nonspecific ligands, allowing selection of fragments that bind proteins with a privileged binding mode, in the absence of any structural data for the protein
Fragment-based screening is an established route to identify low-molecular-weight molecules to gener...
6 páginas, 5 figuras, 1 esquema -- PAGS nros. 17148-17153Competition binding experiments are used in...
Differential epitope mapping saturation transfer difference (DEEP-STD) NMR spectroscopy is a recentl...
STD NMR is a powerful ligand-based tool for screening small molecules and low molecular weight fragm...
Fragment-based drug design is one of the most promising approaches for discovering novel and potent ...
Competition binding experiments are used in NMR-based screenings to match up to the binding site wit...
This review aims to illustrate that STD NMR is not simply a method for drug screening and discovery,...
International audienceFragment-based drug design is one of the most promising approaches for discove...
Fragment-based drug discovery (FBDD) has become a widely accepted tool that is complementary to high...
Fragment-based screening is an established route to identify low-molecular-weight molecules to gener...
Saturation transfer difference (STD) NMR has emerged as one of the most popular ligand-based NMR tec...
Saturation transfer difference (STD) is a valuable tool for studying the binding of small molecules ...
SummaryFragment-based ligand design (FBLD) approaches have become more widely used in drug discovery...
Saturation transfer difference (STD) NMR spectroscopy is extensively used to obtain epitope maps of ...
Saturation transfer difference (STD) is an NMR technique conventionally applied in drug discovery to...
Fragment-based screening is an established route to identify low-molecular-weight molecules to gener...
6 páginas, 5 figuras, 1 esquema -- PAGS nros. 17148-17153Competition binding experiments are used in...
Differential epitope mapping saturation transfer difference (DEEP-STD) NMR spectroscopy is a recentl...
STD NMR is a powerful ligand-based tool for screening small molecules and low molecular weight fragm...
Fragment-based drug design is one of the most promising approaches for discovering novel and potent ...
Competition binding experiments are used in NMR-based screenings to match up to the binding site wit...
This review aims to illustrate that STD NMR is not simply a method for drug screening and discovery,...
International audienceFragment-based drug design is one of the most promising approaches for discove...
Fragment-based drug discovery (FBDD) has become a widely accepted tool that is complementary to high...
Fragment-based screening is an established route to identify low-molecular-weight molecules to gener...
Saturation transfer difference (STD) NMR has emerged as one of the most popular ligand-based NMR tec...
Saturation transfer difference (STD) is a valuable tool for studying the binding of small molecules ...
SummaryFragment-based ligand design (FBLD) approaches have become more widely used in drug discovery...
Saturation transfer difference (STD) NMR spectroscopy is extensively used to obtain epitope maps of ...
Saturation transfer difference (STD) is an NMR technique conventionally applied in drug discovery to...
Fragment-based screening is an established route to identify low-molecular-weight molecules to gener...
6 páginas, 5 figuras, 1 esquema -- PAGS nros. 17148-17153Competition binding experiments are used in...
Differential epitope mapping saturation transfer difference (DEEP-STD) NMR spectroscopy is a recentl...