Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 2243-2245 |
| Seitenumfang | 3 |
| Fachzeitschrift | Angewandte Chemie - International Edition |
| Jahrgang | 38 |
| Ausgabenummer | 15 |
| Publikationsstatus | Veröffentlicht - 28 Juli 1999 |
Abstract
Covalent linkage of the arginine-rich fragment of the Tat protein to 1,4,7,10-tetraazacyclododecane (cyclen) results in the selective cleavage of the TAR-RNA of HIV-1 (see picture; the biotin at the 5' end acts as a label for the subsequent analysis of the cleavage fragments). The cleavage occurs at room temperature and is diminished when Eu(III) ions are present - at a concentration of about 1/10 of the concentration of the peptide-cyclen conjugate. The pH dependence indicates that two ammonium ions are responsible for the cleavage reaction. The white arrows in the schematic diagram mark the cleavage sites in RNaseT1, and the black arrows the sites in the peptide- cyclen conjugate.
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- Chemische Verfahrenstechnik (insg.)
- Katalyse
- Chemie (insg.)
Ziele für nachhaltige Entwicklung
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in: Angewandte Chemie - International Edition, Jahrgang 38, Nr. 15, 28.07.1999, S. 2243-2245.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Selective cleavage of the HIV-1 TAR-RNA with a peptide-cyclen conjugate
AU - Michaelis, Katrin
AU - Kalesse, Markus
PY - 1999/7/28
Y1 - 1999/7/28
N2 - Covalent linkage of the arginine-rich fragment of the Tat protein to 1,4,7,10-tetraazacyclododecane (cyclen) results in the selective cleavage of the TAR-RNA of HIV-1 (see picture; the biotin at the 5' end acts as a label for the subsequent analysis of the cleavage fragments). The cleavage occurs at room temperature and is diminished when Eu(III) ions are present - at a concentration of about 1/10 of the concentration of the peptide-cyclen conjugate. The pH dependence indicates that two ammonium ions are responsible for the cleavage reaction. The white arrows in the schematic diagram mark the cleavage sites in RNaseT1, and the black arrows the sites in the peptide- cyclen conjugate.
AB - Covalent linkage of the arginine-rich fragment of the Tat protein to 1,4,7,10-tetraazacyclododecane (cyclen) results in the selective cleavage of the TAR-RNA of HIV-1 (see picture; the biotin at the 5' end acts as a label for the subsequent analysis of the cleavage fragments). The cleavage occurs at room temperature and is diminished when Eu(III) ions are present - at a concentration of about 1/10 of the concentration of the peptide-cyclen conjugate. The pH dependence indicates that two ammonium ions are responsible for the cleavage reaction. The white arrows in the schematic diagram mark the cleavage sites in RNaseT1, and the black arrows the sites in the peptide- cyclen conjugate.
KW - Macrocycles
KW - Nucleic acids
KW - Peptides
KW - RNA
UR - http://www.scopus.com/inward/record.url?scp=0033517092&partnerID=8YFLogxK
U2 - 10.1002/(SICI)1521-3773(19990802)38:15<2243::AID-ANIE2243>3.0.CO;2-V
DO - 10.1002/(SICI)1521-3773(19990802)38:15<2243::AID-ANIE2243>3.0.CO;2-V
M3 - Article
AN - SCOPUS:0033517092
VL - 38
SP - 2243
EP - 2245
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
SN - 1433-7851
IS - 15
ER -