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PMID: 10471739 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Hypersensitive substrate for ribonucleases.

Nucleic acids research ·Vol. 27 ·No. 18 ·1999-09-15 ·Pages 3696-701

Kelemen BR, Klink TA, Behlke MA, Eubanks SR, Leland PA, Raines RT

Abstract

A substrate for a hypersensitive assay of ribonucleolytic activity was developed in a systematic manner. This substrate is based on the fluorescence quenching of fluorescein held in proximity to rhodamine by a single ribonucleotide embedded within a series of deoxynucleotides. When the substrate is cleaved, the fluorescence of fluorescein is manifested. The optimal substrate is a tetranucleotide with a 5',6-carboxyfluorescein label (6-FAM) and a 3',6-carboxy-tetramethylrhodamine (6-TAMRA) label: 6-FAM-dArUdAdA-6-TAMRA. The fluorescence of this substrate increases 180-fold upon cleavage. Bovine pancreatic ribonuclease A (RNase A) cleaves this substrate with a k (cat)/ K (m)of 3.6 x 10(7)M(-1)s(-1). Human angiogenin, which is a homolog of RNase A that promotes neovascularization, cleaves this substrate with a k (cat)/ K (m)of 3. 3 x 10(2)M(-1)s(-1). This value is >10-fold larger than that for other known substrates of angio-genin. With these attributes, 6-FAM-dArUdAdA-6-TAMRA is the most sensitive known substrate for detecting ribo-nucleolytic activity. This high sensitivity enables a simple protocol for the rapid determination of the inhibition constant ( K (i)) for competitive inhibitors such as uridine 3'-phosphate and adenosine 5'-diphos-phate.

MeSH Terms
Adenosine Diphosphate/metabolism,pharmacology Animals Cattle Deoxyadenosines/chemistry,metabolism Fluoresceins/chemistry,metabolism Fluorescence Fluorescent Dyes/chemistry,metabolism Humans Kinetics Proteins/antagonists & inhibitors,metabolism Pyrimidines/chemistry,metabolism Rhodamines/chemistry,metabolism Ribonuclease, Pancreatic/antagonists & inhibitors,metabolism Sensitivity and Specificity Thermodynamics Uridine Monophosphate/metabolism,pharmacology
Chemicals
5-carboxytetramethylrhodamine succinimidyl ester Deoxyadenosines Fluoresceins Fluorescent Dyes Proteins Pyrimidines Rhodamines 6-carboxyfluorescein Adenosine Diphosphate Uridine Monophosphate angiogenin Ribonuclease, Pancreatic pyrimidine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kelemen B R
Department of Biochemistry, University of Wisconsin-Madison, WI 53706, USA.
Klink T A
Behlke M A
Eubanks S R
Leland P A
Raines R T
Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
1362-4962
Published
1999-09-15
Pages
3696-701
Language
English
Region
England
NLM ID
0411011
PMCID
PMC148625
Subset
IM
Grants
NIGMS NIH HHS · T32GM07215 · United States
NIGMS NIH HHS · T32GM08506 · United States
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