Literature DB >> 18288633

Facile detection of specific RNA-polypeptide interactions by MALDI-TOF mass spectrometry.

Maki Sugaya1, Ryota Saito, Yuriko Matsumura, Kazuo Harada, Akira Katoh.   

Abstract

A simple method for the detection of specific RNA-polypeptide interactions using MALDI-TOF mass spectroscopy is described. Instead of direct observation of the RNA-polypeptide complex, we attempted the indirect observation of the binding event by focusing on the disappearance of the free polypeptide signal upon interaction with RNA. As a result, specific binding of the Rev-response element (RRE) RNA of the HIV with two RRE-binding peptide aptamers, DLA and RLA peptides, as well as the bacteriophage lambda boxB RNA with the lambda N peptide was observed. We also show that specific RNA-binding peptides can be identified from a mixture of peptides with varying RNA-binding affinity, showing that the method could be applied to high-throughput screening from simple peptide libraries. The method described in this study provides a quick and simple method for detecting specific RNA-polypeptide interactions that avoids difficulties associated with direct observation of RNA and RNA-polypeptide complexes, which may find various applications in the analysis of RNA-polypeptide interactions and in the identification of novel RNA-binding polypeptides. Copyright (c) 2008 European Peptide Society and John Wiley & Sons, Ltd.

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Year:  2008        PMID: 18288633     DOI: 10.1002/psc.1021

Source DB:  PubMed          Journal:  J Pept Sci        ISSN: 1075-2617            Impact factor:   1.905


  1 in total

1.  Investigation of calmodulin-Peptide interactions using matrix-assisted laser desorption/ionization mass spectrometry.

Authors:  Zhaofu Wang; Xiaomin Yu; Meng Cui; Zhiqiang Liu; Fengrui Song; Shuying Liu
Journal:  J Am Soc Mass Spectrom       Date:  2008-11-27       Impact factor: 3.109

  1 in total

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