Triple Helix Formation with Short Oligonucleotide-Intercalator Conjugates Matching the HIV-1 U3 LTR End Sequence
| Autor: | M. Le Bret, Jean-François Mouscadet, F. Subra, Hélène Goulaouic, Christian Auclair, C. Ketterle, S. Carteau |
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| Rok vydání: | 1994 |
| Předmět: |
Models
Molecular Base Sequence Molecular model Stereochemistry Oligonucleotide Molecular Sequence Data Carbazoles Temperature Hydrogen-Ion Concentration Biology Chromophore Biochemistry Intercalating Agents Footprinting chemistry.chemical_compound Oligodeoxyribonucleotides chemistry DNA Viral HIV-1 Nucleic Acid Conformation HIV Long Terminal Repeat Linker DNA Triple helix |
| Zdroj: | Biochemistry. 33:4187-4196 |
| ISSN: | 1520-4995 0006-2960 |
| DOI: | 10.1021/bi00180a011 |
| Popis: | In an attempt to target short purine sequences in view of pharmacological application, we have synthesized three new TFO (triple-helix-forming oligonucleotide) conjugates in which an intercalating oxazolopyridocarbazole (OPC) chromophore is linked by a pentamethylene linker to a 7-mer oligonucleotide matching the polypurine/polypyrimidine sequence located in the HIV-1 U3 LTR end region. The TFO moiety of conjugates are 5'CCTTCCC, 5'GGGAAGG, and 5'GGGTTGG. Their ability to bind to double-stranded DNA targets was examined. This binding is demonstrated by a footprinting technique using DNase I as a cleaving agent. The complex involved intermolecular pyr-pur*pyr or pur-pur*pyr triple helix. Pyrimidine TFO-OPC binds in a pH-dependent manner, whereas the others do not. The formation of the complex has been investigated at neutral pH and increasing temperature. We observed that the protection due to the purine and mixed TFO-OPC was pH independent and remained identical up to 40 degrees C. To determine the position of the OPC chromophore, molecular modeling was undertaken on the purine-conjugate/target complex. It has been suggested that the complex involved the intercalation of the OPC at the triplex-duplex junction with a small unwinding at the next excluded site. |
| Databáze: | OpenAIRE |
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