Partial Alloc-Deprotection Approach for Ladder Synthesis of “One-Bead One-Compound” Combinatorial Libraries
- 7 January 2005
- journal article
- Published by American Chemical Society (ACS) in Journal of Combinatorial Chemistry
- Vol. 7 (2) , 197-209
- https://doi.org/10.1021/cc049887b
Abstract
The topologically segregated bilayer-bead concept has been applied to encoded “one-bead one-compound” (OBOC) combinatorial libraries to avoid the interference of coding tags with biological screening. In this paper, we report on the development of a novel partial Alloc-deprotection (PAD) approach and the use of this approach to establish a new ladder-synthesis method for OBOC combinatorial libraries to further exploit the concept. In the PAD approach, Alloc-protected beads are partially deprotected, sequentially layer by layer, starting from the outer layer toward the bead interior. The degree of deprotection (or thickness of each layer) is controlled by the time of exposure to the deprotecting agent, palladium. By repetitive use of the PAD approach, a small portion of Alloc-protected N termini in the bead interior is liberated in each synthetic cycle for generation of an additional ladder member such that each library bead will carry a full-length library compound on the bead surface and a series of truncated ladder members in the bead interior. For the libraries containing isobaric residues, a simple encoding strategy is introduced in the ladder-synthesis method so that the isobaric residues can be differentiated by the coding tags. One advantage of this encoding strategy is that the coding tags are confined together with the truncated ladder members in the bead interior, thus maintaining the arrangement that only the library compounds are displayed on the bead surface. The PAD approach of forming multiple concentric functional layers inside a bead is simple, reliable, and may have other applications in addition to OBOC combinatorial library bead encoding, such as the development of novel optically encoded beads for multiplex immunodiagnostics or even information recording.Keywords
This publication has 11 references indexed in Scilit:
- Multilayer Transfer Printing for Polyelectrolyte Multilayer Patterning: Direct Transfer of Layer‐by‐Layer Assembled Micropatterned Thin FilmsAdvanced Materials, 2004
- 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
- Production, Analysis, and Application of Spatially Resolved Shells in Solid-Phase Polymer SpheresJournal of the American Chemical Society, 2002
- Oligosaccharide Mimetics Obtained by Novel, Rapid Screening of Carboxylic Acid Encoded Glycopeptide LibrariesJournal of the American Chemical Society, 1998
- CNBr/Formic Acid Reactions of Methionine- and Trifluoromethionine-Containing Lambda Lysozyme: Probing Chemical and Positional Reactivity and Formylation Side Reactions by Mass SpectrometryProtein Journal, 1998
- Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditionsPublished by Elsevier ,1998
- Protein Ladder SequencingScience, 1993
- Generation and use of synthetic peptide combinatorial libraries for basic research and drug discoveryNature, 1991
- Solid phase peptide synthesis utilizing 9‐fluorenylmethoxycarbonyl amino acidsInternational Journal of Peptide and Protein Research, 1990