Literature DB >> 11869795

Microbial identification by immunohybridization assay of artificial RNA labels.

Katerina D Kourentzi1, George E Fox, Richard C Willson.   

Abstract

Ribosomal RNA (rRNA) and engineered stable artificial RNAs (aRNAs) are frequently used to monitor bacteria in complex ecosystems. In this work, we describe a solid-phase immunocapture hybridization assay that can be used with low molecular weight RNA targets. A biotinylated DNA probe is efficiently hybridized in solution with the target RNA, and the DNA-RNA hybrids are captured on streptavidin-coated plates and quantified using a DNA-RNA heteroduplex-specific antibody conjugated to alkaline phosphatase. The assay was shown to be specific for both 5S rRNA and low molecular weight (LMW) artificial RNAs and highly sensitive, allowing detection of as little as 5.2 ng (0.15 pmol) in the case of 5S rRNA. Target RNAs were readily detected even in the presence of excess nontarget RNA. Detection using DNA probes as small as 17 bases targeting a repetitive artificial RNA sequence in an engineered RNA was more efficient than the detection of a unique sequence.

Keywords:  NASA Discipline Environmental Health; Non-NASA Center

Mesh:

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Year:  2002        PMID: 11869795     DOI: 10.1016/s0167-7012(02)00006-4

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  1 in total

1.  Effect of an artificial RNA marker on gene expression in Escherichia coli.

Authors:  Don L Tucker; Fathi Karouia; Jim Wang; Yi Luo; Tong-Bin Li; Richard C Willson; Yuriy Fofanov; George E Fox
Journal:  Appl Environ Microbiol       Date:  2005-07       Impact factor: 4.792

  1 in total

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