Abstract
A microfluidic chip based method utilized for effective screening of high-throughput peptide libraries was achieved. Continuous flow bead trapping, sorting, arraying and in situ sequencing was integrated. Peptide library screening with 105 beads was processed within 4 hours and peptide ligands toward the target protein AHA and APN were successfully discovered.
Original language | English |
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Pages (from-to) | 61767-61770 |
Number of pages | 4 |
Journal | RSC Advances |
Volume | 4 |
Issue number | 106 |
DOIs | |
Publication status | Published - 2014 |
Externally published | Yes |