DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.

We have prepared triplex-forming oligonucleotides containing the nucleotide analogue 5-dimethylaminopropargyl deoxyuridine (DMAPdU) in place of thymidine and examined their ability to form intermolecular triple helices by thermal melting and DNase I footprinting studies. The results were compared wi...

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Asıl Yazarlar: Rusling, D, Peng, G, Srinivasan, N, Fox, K, Brown, T
Materyal Türü: Journal article
Dil:English
Baskı/Yayın Bilgisi: 2009
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author Rusling, D
Peng, G
Srinivasan, N
Fox, K
Brown, T
author_facet Rusling, D
Peng, G
Srinivasan, N
Fox, K
Brown, T
author_sort Rusling, D
collection OXFORD
description We have prepared triplex-forming oligonucleotides containing the nucleotide analogue 5-dimethylaminopropargyl deoxyuridine (DMAPdU) in place of thymidine and examined their ability to form intermolecular triple helices by thermal melting and DNase I footprinting studies. The results were compared with those for oligonucleotides containing 5-aminopropargyl-dU (APdU), 5-guanidinopropargyl-dU (GPdU) and 5-propynyl dU (PdU). We find that DMAPdU enhances triplex stability relative to T, though slightly less than the other analogues that bear positive charges (T << PdU < DMAPdU < APdU < GPdU). For oligonucleotides that contain multiple substitutions with DMAPdU dispersed residues are more effective than clustered combinations. DMAPdU will be especially useful as a nucleotide analogue as, unlike APdU and GPdU, the base does not require protection during oligonucleotide synthesis and it can therefore be used with other derivatives that require mild deprotection conditions.
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spelling oxford-uuid:ecebf8f4-ad8b-4209-8df3-feb4020edf1c2022-03-27T11:21:04ZDNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ecebf8f4-ad8b-4209-8df3-feb4020edf1cEnglishSymplectic Elements at Oxford2009Rusling, DPeng, GSrinivasan, NFox, KBrown, TWe have prepared triplex-forming oligonucleotides containing the nucleotide analogue 5-dimethylaminopropargyl deoxyuridine (DMAPdU) in place of thymidine and examined their ability to form intermolecular triple helices by thermal melting and DNase I footprinting studies. The results were compared with those for oligonucleotides containing 5-aminopropargyl-dU (APdU), 5-guanidinopropargyl-dU (GPdU) and 5-propynyl dU (PdU). We find that DMAPdU enhances triplex stability relative to T, though slightly less than the other analogues that bear positive charges (T << PdU < DMAPdU < APdU < GPdU). For oligonucleotides that contain multiple substitutions with DMAPdU dispersed residues are more effective than clustered combinations. DMAPdU will be especially useful as a nucleotide analogue as, unlike APdU and GPdU, the base does not require protection during oligonucleotide synthesis and it can therefore be used with other derivatives that require mild deprotection conditions.
spellingShingle Rusling, D
Peng, G
Srinivasan, N
Fox, K
Brown, T
DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.
title DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.
title_full DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.
title_fullStr DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.
title_full_unstemmed DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.
title_short DNA triplex formation with 5-dimethylaminopropargyl deoxyuridine.
title_sort dna triplex formation with 5 dimethylaminopropargyl deoxyuridine
work_keys_str_mv AT ruslingd dnatriplexformationwith5dimethylaminopropargyldeoxyuridine
AT pengg dnatriplexformationwith5dimethylaminopropargyldeoxyuridine
AT srinivasann dnatriplexformationwith5dimethylaminopropargyldeoxyuridine
AT foxk dnatriplexformationwith5dimethylaminopropargyldeoxyuridine
AT brownt dnatriplexformationwith5dimethylaminopropargyldeoxyuridine