Literature DB >> 1719428

Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery.

R A Houghten1, C Pinilla, S E Blondelle, J R Appel, C T Dooley, J H Cuervo.   

Abstract

Existing methods for the synthesis and screening of large numbers of peptides are limited by their inability to generate and screen the requisite number (millions) of individual peptides and/or their inability to generate unmodified free peptides in quantities able to interact in solution. We have circumvented these limitations by developing synthetic peptide combinatorial libraries composed of mixtures of free peptides in quantities which can be used directly in virtually all existing assay systems. The screening of these heterogeneous libraries, along with an iterative selection and synthesis process, permits the systematic identification of optimal peptide ligands. Starting with a library composed of more than 34 million hexa-peptides, we present here the precise identification of an antigenic determinant recognized by a monoclonal antibody as well as the straightforward development of new potent antimicrobial peptides.

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Year:  1991        PMID: 1719428     DOI: 10.1038/354084a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  204 in total

1.  Use of combinatorial library screening to identify inhibitors of a bacterial two-component signal transduction kinase.

Authors:  S Roychoudhury; S E Blondelle; S M Collins; M C Davis; H D McKeever; R A Houghten; C N Parker
Journal:  Mol Divers       Date:  1998       Impact factor: 2.943

2.  Global analysis of proteasomal substrate specificity using positional-scanning libraries of covalent inhibitors.

Authors:  T Nazif; M Bogyo
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

3.  N-Acylated and D enantiomer derivatives of a nonamer core peptide of lactoferricin B showing improved antimicrobial activity.

Authors:  H Wakabayashi; H Matsumoto; K Hashimoto; S Teraguchi; M Takase; H Hayasawa
Journal:  Antimicrob Agents Chemother       Date:  1999-05       Impact factor: 5.191

4.  Sample size determination in combinatorial chemistry.

Authors:  P L Zhao; R Zambias; J A Bolognese; D Boulton; K Chapman
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-24       Impact factor: 11.205

5.  A revolution in drug discovery. Combinatorial chemistry still needs logic to drive science forward.

Authors:  N Beeley; A Berger
Journal:  BMJ       Date:  2000-09-09

6.  Characterization of oligodeoxyribonucleotide synthesis on glass plates.

Authors:  E LeProust; H Zhang; P Yu; X Zhou; X Gao
Journal:  Nucleic Acids Res       Date:  2001-05-15       Impact factor: 16.971

7.  Specificity and affinity motifs for Grb2 SH2-ligand interactions.

Authors:  Helmut W H G Kessels; Alister C Ward; Ton N M Schumacher
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-25       Impact factor: 11.205

8.  Screening one bead one compound libraries against serum using a flow cytometer: Determination of the minimum antibody concentration required for ligand discovery.

Authors:  Osayemwenre Erharuyi; Scott Simanski; Patrick J McEnaney; Thomas Kodadek
Journal:  Bioorg Med Chem Lett       Date:  2018-01-31       Impact factor: 2.823

9.  Method for screening and MALDI-TOF MS sequencing of encoded combinatorial libraries.

Authors:  Bi-Huang Hu; Marsha Ritter Jones; Phillip B Messersmith
Journal:  Anal Chem       Date:  2007-08-23       Impact factor: 6.986

10.  Rational screening of oligonucleotide combinatorial libraries for drug discovery.

Authors:  D J Ecker; T A Vickers; R Hanecak; V Driver; K Anderson
Journal:  Nucleic Acids Res       Date:  1993-04-25       Impact factor: 16.971

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