Decoding a PNA Encoded Peptide Library by PCR: The Discovery of New Cell Surface Receptor Ligands

被引:45
作者
Svensen, Nina [1 ]
Diaz-Mochon, Juan Jose [1 ]
Bradley, Mark [1 ]
机构
[1] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
来源
CHEMISTRY & BIOLOGY | 2011年 / 18卷 / 10期
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
SMALL-MOLECULE MICROARRAYS; COMBINATORIAL CHEMISTRY; CHEMICAL LIBRARIES; GLIOMA-CELLS; NUCLEIC-ACID; SELECTION; IDENTIFICATION; INTEGRIN; DELIVERY; DESIGN;
D O I
10.1016/j.chembiol.2011.07.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ability to screen and identify new ligands for cell surface receptors has been a long-standing goal as it might allow targeting of pharmaceutically relevant receptors, such as integrins or G protein coupled receptors. Here, we present a method to amplify hits from a library of PNA-tagged peptides. To this end, human cells, overexpressing either integrins or the CCR6 receptor, were treated with a 10,000 member PNA-encoded peptide library. Extraction of the PNA tags from the surface of the cells was followed by a PNA-tag to DNA translation and amplification enabling decoding of the tags via microarray hybridization. This approach to ligand discovery facilitates screening for differences in surface-receptor ligands and/or receptor expression between different cell types, and opens up a practical approach to PNA-tag amplification.
引用
收藏
页码:1284 / 1289
页数:6
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