Direct Identification of On-Bead Peptides Using Surface-Enhanced Raman Spectroscopic Barcoding System for High-Throughput Bioanalysis

Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding and optical encoding have b...

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Published in:Scientific reports Vol. 5; no. 1; p. 10144
Main Authors: Kang, Homan, Jeong, Sinyoung, Koh, Yul, Geun Cha, Myeong, Yang, Jin-Kyoung, Kyeong, San, Kim, Jaehi, Kwak, Seon-Yeong, Chang, Hye-Jin, Lee, Hyunmi, Jeong, Cheolhwan, Kim, Jong-Ho, Jun, Bong-Hyun, Kim, Yong-Kweon, Hong Jeong, Dae, Lee, Yoon-Sik
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 28-05-2015
Nature Publishing Group
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Summary:Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding and optical encoding have been reported to identify those libraries. In this paper, a simple and efficient surface-enhanced Raman spectroscopic (SERS) barcoding method using highly sensitive SERS nanoparticles (SERS ID) is presented. The 44 kinds of SERS IDs were able to generate simple codes and could possibly generate more than one million kinds of codes by incorporating combinations of different SERS IDs. The barcoding method exhibited high stability and reliability under bioassay conditions. The SERS ID encoding based screening platform can identify the peptide ligand on the bead and also quantify its binding affinity for specific protein. We believe that our SERS barcoding technology is a promising method in the screening of one-bead-one-compound (OBOC) libraries for drug discovery.
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These authors contributed equally to this work.
Current address: Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215, United States
Current address: Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep10144