Encoding Method for OBOC Small Molecule Libraries Using a Biphasic Approach for Ladder-Synthesis of Coding Tags
- 16 April 2004
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 126 (18), 5740-5749
- https://doi.org/10.1021/ja049322j
Abstract
In the “one-bead one-compound” (OBOC) combinatorial library method, each compound bead displays only one compound entity. Hundreds of thousands to millions of compound beads can be synthesized rapidly and screened simultaneously. Positive compound beads are then isolated for structural analysis. To fully exploit the power of OBOC combinatorial small molecule libraries, a robust and high throughput encoding method is needed to decode the positive compound beads. In this paper, we report on the development of a novel encoding strategy that combines the concepts of ladder-synthesis and chemical encoding on bilayer beads. In these encoded libraries, small molecule compounds are displayed on the bead surface, and cleavable coding tags consisting of a series of truncated molecules reside in the bead interior. Such a library can be easily constructed using the biphasic approach (J. Am. Chem. Soc. 2002, 124, 7678) to topologically segregate the functionalities of the beads during library synthesis. The ladder members and coding tags are then released for MALDI-TOF-MS analysis. To simplify the interpretation of the mass spectra, we purposely add bromine into the cleavable linker so that the cleavage products generate a characteristic isotope fingerprint. The chemical structure of library compounds can be determined by analyzing the mass differences between adjacent peaks on the mass spectra. This encoding strategy also provides valuable information on the quality of the testing compound on the surface of the bead. To validate this methodology, a model OBOC small molecule library with 12,288 members was synthesized on TentaGel beads and screened against streptavidin. The chemical structures of the compound on each positive bead were unambiguously identified.Keywords
This publication has 13 references indexed in Scilit:
- High-Throughput One-Bead-One-Compound Approach to Peptide-Encoded Combinatorial Libraries: MALDI-MS Analysis of Single TentaGel BeadsJournal of Combinatorial Chemistry, 2003
- Identification of oxidized methionine residues in peptides containing two methionine residues by derivatization and matrix-assisted laser desorption/ionization mass spectrometryProteomics, 2002
- Protecting Groups in Solid-Phase Organic SynthesisJournal of Combinatorial Chemistry, 2001
- Solutions for library encoding to create collections of discrete compoundsCurrent Opinion in Chemical Biology, 2001
- Solid-phase synthesis of N-hydroxyindoles and benzo[c]isoxazoles by C-arylation of substituted acetonitriles and 1,3-dicarbonyl compounds with polystyrene-bound aryl fluoridesTetrahedron Letters, 1999
- Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditionsTetrahedron Letters, 1997
- Enzyme-mediated spatial segregation on individual polymeric support beads: application to generation and screening of encoded combinatorial libraries.Proceedings of the National Academy of Sciences, 1996
- Protein Ladder SequencingScience, 1993
- Generation and use of synthetic peptide combinatorial libraries for basic research and drug discoveryNature, 1991
- General method for rapid synthesis of multicomponent peptide mixturesInternational Journal of Peptide and Protein Research, 1991