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Purification of native and recombinant double-stranded RNA-specific adenosine deaminases.

O'Connell, MA, Gerber, A and Keegan, LP (1998) Purification of native and recombinant double-stranded RNA-specific adenosine deaminases. Methods, 15 (1). pp. 51-62.

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Abstract

ADAR1 and ADAR2 are members of a family of enzymes that catalyze the conversion of adenosine to inosine in double-stranded RNA. Unlike the other types of RNA editing that involve multiprotein editing complexes, the site-specific deamination of an adenosine to inosine is catalyzed by single enzymes. ADAR1 and ADAR2 have been purified and the genes cloned from various sources. Each gene encodes multiple splice variants. As it is crucial to have an adequate supply of pure protein to investigate this type of RNA editing, we describe in this article methods for both the purification and the overexpression of either full-length or partial ADAR1 and ADAR2 isoforms.

Item Type: Article
Authors :
NameEmailORCID
O'Connell, MAUNSPECIFIEDUNSPECIFIED
Gerber, Aa.gerber@surrey.ac.ukUNSPECIFIED
Keegan, LPUNSPECIFIEDUNSPECIFIED
Date : May 1998
Identification Number : 10.1006/meth.1998.0605
Uncontrolled Keywords : Adenosine Deaminase, Amino Acid Sequence, Animals, Antibodies, Base Sequence, Cattle, Chromatography, Affinity, Chromatography, Ion Exchange, DNA, Recombinant, Electrophoresis, Polyacrylamide Gel, Escherichia coli, HeLa Cells, Humans, Molecular Sequence Data, Pichia, RNA, Double-Stranded, Recombinant Proteins, Substrate Specificity, Thymus Gland
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 10:13
Last Modified : 17 May 2017 14:48
URI: http://epubs.surrey.ac.uk/id/eprint/826912

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