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Particle-Based Synthesis of Peptide Arrays

✍ Scribed by Frank Breitling; Thomas Felgenhauer; Alexander Nesterov; Volker Lindenstruth; Volker Stadler; F. Ralf Bischoff


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
427 KB
Volume
10
Category
Article
ISSN
1439-4227

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

High‐density peptide arrays with solid amino acid particles: Intermittent “freezing” of activated amino acid derivatives within solid particles allows a laser printer or a chip to spatially address these “postal packages”. Subsequent parallel coupling is started simply by melting a whole layer of 20 different amino acid particles, freeing the hitherto immobilized amino acids and resulting in the coupling of all 20 different amino acids to the support in a single coupling step.magnified image

Lithographic methods allow for the combinatorial synthesis of >50 000 oligonucleotides per cm^2^, and this has revolutionized the field of genomics. High‐density peptide arrays promise to advance the field of proteomics in a similar way, but currently lag behind. This is mainly due to the monomer‐by‐monomer repeated consecutive coupling of 20 different amino acids associated with lithography, which adds up to an excessive number of coupling cycles. Combinatorial synthesis based on electrically charged solid amino acid particles resolves this problem. A color laser printer or a chip addresses the different charged particles consecutively to a solid support, where, when completed, the whole layer of solid amino acid particles is melted at once. This frees hitherto immobilized amino acids to couple all 20 different amino acids to the support in one single coupling reaction. The method should allow for the translation of entire genomes into sets of overlapping peptides to be used in proteome research.


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