A High-Density Screening Format for Encoded Combinatorial Libraries: Assay Miniaturization and Its Application to Enzymatic Reactions

• Published in: Analytical biochemistry 1997-03, Vol.246 (1), p.20-29
• Main Authors: Schullek, John R., Butler, John H., Ni, Zhi-Jie, Chen, Dawn, Yuan, Zhengyu
• Format: Article
• Language: English
• Subjects: Acylation; Diffusion; Enzymes - chemistry; Humans; Matrix Metalloproteinase 7; Metalloendopeptidases - chemistry; Miniaturization; Peptide Library; Peptide Mapping - methods; Polystyrenes; Spectrometry, Fluorescence
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1006/abio.1996.9958

A novel, miniaturized high-throughput screening format is described for assay of combinatorial libraries generated on beads. This approach, which is ideally suited to encoded libraries synthesized on beads, utilizes the photolytic cleavage of individual compounds into a high-density well array (>6500 wells within a standard 96-well microtiter plate footprint) with well volumes as low as 0.37 μl. As a model study, an encoded dipeptide library (324 members) acylated with isobutyl succinate was assayed using this format to search for potential inhibitors of matrilysin, a member of the matrix metalloproteinase superfamily.In siturelease of compounds from solid support was accomplished by photochemical cleavage after beads and enzyme were distributed to the wells. After the addition of a fluorogenic substrate to the array, the extent of enzyme inhibition and identification of active compounds was quantitated by imaging of the fluorescence emission upon uv irradiation. The structure–activity relationship data generated from the identified inhibitors in this study corroborate previous findings, thus validating the utility of this approach as a means of high-throughput screening of bead-based libraries.