Literature DB >> 17035011

Screening of alpha-helical peptide ligands controlling a calcineurin-phosphatase activity.

Kenji Usui1, Kin-Ya Tomizaki, Hisakazu Mihara.   

Abstract

In this paper, we describe an application of 202-membered fluorescently labeled peptide library designed to take an alpha-helix secondary structure. As a proof-of-concept experiment, a calmodulin (CaM)/calcineurin (Cn) pair was chosen to screen alpha-helical peptide ligands that tightly bind to CaM and also control enzymatic functions of Cn. Three peptides were successfully selected from the library by assaying Cn-phosphatase activities and peptide-CaM interactions (dual check process). The strategy using a designed peptide library shows real promise as a peptide-based high-throughput screening system.

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Year:  2006        PMID: 17035011     DOI: 10.1016/j.bmcl.2006.09.075

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  Electron capture dissociation product ion abundances at the X amino acid in RAAAA-X-AAAAK peptides correlate with amino acid polarity and radical stability.

Authors:  Aleksey Vorobyev; Hisham Ben Hamidane; Yury O Tsybin
Journal:  J Am Soc Mass Spectrom       Date:  2009-09-03       Impact factor: 3.109

2.  Use of a designed Peptide library to screen for binders to a particular DNA g-quadruplex sequence.

Authors:  Keita Kobayashi; Noriko Matsui; Kenji Usui
Journal:  J Nucleic Acids       Date:  2011-09-06

Review 3.  Label and Label-Free Detection Techniques for Protein Microarrays.

Authors:  Amir Syahir; Kenji Usui; Kin-Ya Tomizaki; Kotaro Kajikawa; Hisakazu Mihara
Journal:  Microarrays (Basel)       Date:  2015-04-24
  3 in total

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