2003
DOI: 10.1007/s00216-003-1876-3
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Epitope-targeted proteome analysis: towards a large-scale automated protein?protein-interaction mapping utilizing synthetic peptide arrays

Abstract: We describe the development of a process for the genome-wide mapping of interactions between protein domains and peptide ligands entirely based on high-throughput biochip technologies. A phage library displaying protein domains from a randomly fragmented and cloned cDNA library will be "panned" on an array of synthetic peptide ligands. After multiplexed affinity enrichment, peptide-specific phage populations will be automatically eluted, propagated, labelled and identified by hybridisation to a DNA microarray.… Show more

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Cited by 33 publications
(18 citation statements)
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“…For example, epitope specific antibodies can be isolated from polyclonal sera [28,29], thus, combining monospecificity with the ease of rabbit serum preparation. More recent novel options include, e.g., the preparation of miniprotein (protein domain) arrays by combination of solid phase synthesis and chemical ligation [30] or the multiplexed biopanning of phage libraries for genome wide protein interaction mapping [31].…”
Section: Other Protein Ligand Interactionsmentioning
confidence: 99%
“…For example, epitope specific antibodies can be isolated from polyclonal sera [28,29], thus, combining monospecificity with the ease of rabbit serum preparation. More recent novel options include, e.g., the preparation of miniprotein (protein domain) arrays by combination of solid phase synthesis and chemical ligation [30] or the multiplexed biopanning of phage libraries for genome wide protein interaction mapping [31].…”
Section: Other Protein Ligand Interactionsmentioning
confidence: 99%
“…Bialek et al described the development of a process for the genome-wide mapping of interactions between protein domains and peptide ligands entirely based on high-throughput microarray technology. [159] It is possible to attach a phage library displaying protein domains from a randomly fragmented and cloned complementary DNA (cDNA) library onto a peptide microarray; peptide-specific phage populations are then automatically eluted, propagated, labeled, and identified by hybridization to a DNA microarray after multiple enrichment. Takahashi et al constructed a novel protein-detection system in which 126 de novo peptides designed to form loop structures were labeled site-specifically with a fluorescent dye and immobilized into 96-well plastic plates.…”
Section: Peptide Microarraysmentioning
confidence: 99%
“…The authors "panned" a phage library displaying protein domains from a randomly fragmented and cloned cDNAlibrary on an array of synthetic peptide ligands. After multiplexed affinity enrichment, peptide specific phage populations will be automatically eluted, propagated, labeled and identified by hybridization to a DNA-microarray [153].…”
Section: Applicationsmentioning
confidence: 99%