RAMPED-UP NMR: multiplexed NMR-based screening for drug discovery
- PMID: 12952475
- DOI: 10.1021/ja0348593
RAMPED-UP NMR: multiplexed NMR-based screening for drug discovery
Abstract
The crucial step in drug discovery is the identification of a lead compound from a vast chemical library by any number of screening techniques. NMR-based screening has the advantage of directly detecting binding of a compound to the target. The spectra resulting from these screens can also be very complex and difficult to analyze, making this an inefficient process. We present here a method, RAMPED-UP NMR, (Rapid Analysis and Multiplexing of Experimentally Discriminated Uniquely Labeled Proteins using NMR) which generates simple spectra which are easy to interpret and allows several proteins to be screened simultaneously. In this method, the proteins to be screened are uniquely labeled with one amino acid type. There are several benefits derived from this unique labeling strategy: the spectra are greatly simplified, resonances that are most likely to be affected by binding are the only ones observed, and peaks that yield little or no information upon binding are eliminated, allowing the analysis of multiple proteins easily and simultaneously. We demonstrate the ability of three different proteins to be analyzed simultaneously for binding to two different ligands. This method will have significant impact in the use of NMR spectroscopy for both the lead generation and lead optimization phases of drug discovery by its ability to increase screening throughput and the ability to examine selectivity. To the best of our knowledge, this is the first time in any format that multiple proteins can be screened in one tube.
Similar articles
-
Design and NMR-based screening of LEF, a library of chemical fragments with different local environment of fluorine.J Am Chem Soc. 2009 Sep 16;131(36):12949-59. doi: 10.1021/ja905207t. J Am Chem Soc. 2009. PMID: 19702332
-
Robust NMR screening for lead compounds using tryptophan-containing proteins.J Am Chem Soc. 2009 Jun 10;131(22):7500-1. doi: 10.1021/ja901863h. J Am Chem Soc. 2009. PMID: 19422216
-
NMR in the acceleration of drug discovery.Curr Opin Drug Discov Devel. 2001 Jul;4(4):479-92. Curr Opin Drug Discov Devel. 2001. PMID: 11727313 Review.
-
Nuclear magnetic resonance in target profiling and compound file enhancement.Curr Opin Drug Discov Devel. 2006 Jul;9(4):463-70. Curr Opin Drug Discov Devel. 2006. PMID: 16889229 Review.
-
Use of 19F NMR spectroscopy to screen chemical libraries for ligands that bind to proteins.Org Biomol Chem. 2004 Mar 7;2(5):725-31. doi: 10.1039/b313166a. Epub 2004 Feb 3. Org Biomol Chem. 2004. PMID: 14985813
Cited by
-
A combinatorial selective labeling method for the assignment of backbone amide NMR resonances.J Am Chem Soc. 2004 Apr 28;126(16):5020-1. doi: 10.1021/ja039601r. J Am Chem Soc. 2004. PMID: 15099056 Free PMC article.
-
Advances in Nuclear Magnetic Resonance for Drug Discovery.Expert Opin Drug Discov. 2009 Oct 1;4(10):1077-1098. doi: 10.1517/17460440903232623. Expert Opin Drug Discov. 2009. PMID: 20333269 Free PMC article.
-
High-field solution NMR spectroscopy as a tool for assessing protein interactions with small molecule ligands.J Pharm Sci. 2008 Nov;97(11):4670-95. doi: 10.1002/jps.21378. J Pharm Sci. 2008. PMID: 18351634 Free PMC article. Review.
-
Estimating protein-ligand binding affinity using high-throughput screening by NMR.J Comb Chem. 2008 Nov-Dec;10(6):948-58. doi: 10.1021/cc800122m. Epub 2008 Oct 3. J Comb Chem. 2008. PMID: 18831571 Free PMC article.
-
Target-specific NMR detection of protein-ligand interactions with antibody-relayed 15N-group selective STD.J Biomol NMR. 2016 Dec;66(4):227-232. doi: 10.1007/s10858-016-0076-3. Epub 2016 Nov 24. J Biomol NMR. 2016. PMID: 27885546
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources