esiRNAs purified with chromatography suppress homologous gene expression with high efficiency and specificity.

Abstract:

:Many preclinical studies have shown RNA interference (RNAi) as a new promising way to treat various human diseases including cancer and virus infection and there is an increasing demand for the large-scale preparation of short interfering RNAs (siRNAs) at low cost. Data are accumulating to show that endoribonuclease-prepared siRNAs (esiRNAs) are superior to chemically synthesized siRNAs in terms of expense, efficiency, and specificity. Yet all procedures available for esiRNA purification were designed to produce small amount of siRNAs for laboratory use. In this article, a new method of purification of esiRNAs based on ion exchange chromatography and size exclusion chromatography is reported. The esiRNAs prepared with this method are shown here to be of high purity and specifically suppress homologous gene expression without activating interferon response and with higher efficiency than chemically synthesized siRNAs. We can expect that the new method can be scaled up easily to provide large quantities of esiRNAs to meet the requirement of preclinical and clinical studies.

journal_name

Mol Biotechnol

journal_title

Molecular biotechnology

authors

Xuan B,Qian Z,Tan C,Min T,Shen S,Huang W

doi

10.1385/MB:31:3:203

keywords:

subject

Has Abstract

pub_date

2005-11-01 00:00:00

pages

203-9

issue

3

eissn

1073-6085

issn

1559-0305

pii

MB:31:3:203

journal_volume

31

pub_type

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