Literature DB >> 16880920

Optimized protocols for the isolation of specific protein-binding peptides or peptoids from combinatorial libraries displayed on beads.

Thomas Kodadek1, Kiran Bachhawat-Sikder.   

Abstract

Many methods have been published by which combinatorial libraries may be screened for compounds capable of manipulating the function(s) of a target protein. One of the simplest approaches is to identify compounds in a library that bind the protein of interest, since these binding events usually occur on functionally important surfaces of the protein. These protein-binding compounds could also be of utility as protein capture agents in the construction of protein-detecting microarrays or related analytical devices and as reagents for the affinity purification of proteins from complex mixtures. In this article, we provide optimized methods for screening libraries of molecules displayed on the beads on which they were synthesized. This is a particularly convenient format for library screening for laboratories with limited budgets and modest robotics capabilities.

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Year:  2005        PMID: 16880920     DOI: 10.1039/b514349g

Source DB:  PubMed          Journal:  Mol Biosyst        ISSN: 1742-2051


  20 in total

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4.  High-throughput screening of one-bead-one-compound libraries: identification of cyclic peptidyl inhibitors against calcineurin/NFAT interaction.

Authors:  Tao Liu; Ziqing Qian; Qing Xiao; Dehua Pei
Journal:  ACS Comb Sci       Date:  2011-08-26       Impact factor: 3.784

5.  Solid-phase synthesis and screening of N-acylated polyamine (NAPA) combinatorial libraries for protein binding.

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6.  Accurate MALDI-TOF/TOF sequencing of one-bead-one-compound peptide libraries with application to the identification of multiligand protein affinity agents using in situ click chemistry screening.

Authors:  Su Seong Lee; Jaehong Lim; Sylvia Tan; Junhoe Cha; Shi Yun Yeo; Heather D Agnew; James R Heath
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7.  Aβ42-binding peptoids as amyloid aggregation inhibitors and detection ligands.

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8.  Screening bicyclic peptide libraries for protein-protein interaction inhibitors: discovery of a tumor necrosis factor-α antagonist.

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Review 9.  The identification of high-affinity G protein-coupled receptor ligands from large combinatorial libraries using multicolor quantum dot-labeled cell-based screening.

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Journal:  Future Med Chem       Date:  2014-05       Impact factor: 3.808

10.  Direct Ras Inhibitors Identified from a Structurally Rigidified Bicyclic Peptide Library.

Authors:  Punit Upadhyaya; Ziqing Qian; Nurlaila A A Habir; Dehua Pei
Journal:  Tetrahedron       Date:  2014-10-21       Impact factor: 2.457

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