'On-the-fly' optical encoding of combinatorial peptide libraries for profiling of protease specificity

• Published in: Molecular bioSystems Vol. 6; no. 1; pp. 225 - 233
• Main Authors: Marcon, Lionel, Battersby, Bronwyn J, Rühmann, Andreas, Ford, Kym, Daley, Matthew, Lawrie, Gwendolyn A, Trau, Matt
• Format: Journal Article
• Language: English
• Published: England 01.01.2010
• Subjects: Combinatorial Chemistry Techniques - methods; Flow Cytometry; Models, Theoretical; Peptide Hydrolases - metabolism; Peptide Library; Substrate Specificity
• ISSN: 1742-206X; 1742-2051
• DOI: 10.1039/b909087h

Large solid-phase combinatorial libraries currently play an important role in areas such as infectious disease biomarker discovery, profiling of protease specificity and anticancer drug discovery. Because compounds on solid support beads are not positionally-encoded as they are in microarrays, innovative methods of encoding are required. There are many advantages associated with optical encoding and several strategies have been described in the literature to combine fluorescence encoding methods with solid-phase library synthesis. We have previously introduced an alternative fluorescence-based encoding method ("colloidal barcoding"), which involves encoding 10-20 mum support beads during a split-and-mix synthesis with smaller 0.6-0.8 mum silica colloids that contain specific and identifiable combinations of fluorescent dye. The power of this 'on-the-fly' encoding approach lies in the efficient use of a small number of fluorescent dyes to encode millions of compounds. Described herein, for the first time, is the use of a colloid-barcoded library in a biological assay (i.e., protease profiling) combined with the use of confocal microscopy to decode the colloidal barcode. In this proof-of-concept demonstration, a small focussed peptide library was optically-encoded during a combinatorial synthesis, incubated with a protease (trypsin), analysed by flow cytometry and decoded via confocal microscopy. During assay development, a range of parameters were investigated and optimised, including substrate (or probe) loading, barcode stability, characteristics of the peptide-tagging fluorophore, and spacer group configuration. Through successful decoding of the colloidal barcodes, it was confirmed that specific peptide sequences presenting one or two cleavage sites were recognised by trypsin while peptide sequences not cleavable by trypsin remained intact.