AAT.ATT is the most abundant and also the most frequently polymorphic class of trinucleotide repeats in the human genome, To characterize its structural properties and conformational changes induced by minor groove ligands, (AAT)(6) and (ATT)(6) oligomers as well as their complexes with DAPI were investigated by electrophoretic mobility and UV thermal stability as well as fluorescence and NMR spectroscopy. The results show that individual (AAT)(6) and (ATT)(6) strands exist principally as monomeric non-hydrogen-bonded structures. Their individual interaction with DAPI induces the formation of base-paired structures with different thermal stabilities by quite spectroscopically distinct binding mechanisms. In the presence of DAPI, (ATT)(6) forms a monomeric hairpin structure stabilized by two ligands located in the minor groove with a strong apparent binding constant of 3.4 x 10(6) M-1. The DAPI-induced (ATT)(6) hairpin is characterized by well-stacked A.T Watson-Crick and T.T wobble base pairs, a high electrophoretic mobility, and a melting temperature of 41 degrees C. Interaction of DAPI with the complementary (AAT)(6) strand favors less stable base-paired structures, and the results are consistent with electrostatic and hydrogen-bond interactions of the ligand with the phosphodiester backbone of (AAT)(6) by minor involvement of DNA bases.

Trotta, E., Del Grosso, N., Erba, M., Paci, M. (2000). The ATT strand of AAT center dot ATT trinucleotide repeats adopts stable hairpin structures induced by minor groove binding ligands. BIOCHEMISTRY, 39(23), 6799-6808 [10.1021/bi0001473].

The ATT strand of AAT center dot ATT trinucleotide repeats adopts stable hairpin structures induced by minor groove binding ligands

PACI, MAURIZIO
2000-01-01

Abstract

AAT.ATT is the most abundant and also the most frequently polymorphic class of trinucleotide repeats in the human genome, To characterize its structural properties and conformational changes induced by minor groove ligands, (AAT)(6) and (ATT)(6) oligomers as well as their complexes with DAPI were investigated by electrophoretic mobility and UV thermal stability as well as fluorescence and NMR spectroscopy. The results show that individual (AAT)(6) and (ATT)(6) strands exist principally as monomeric non-hydrogen-bonded structures. Their individual interaction with DAPI induces the formation of base-paired structures with different thermal stabilities by quite spectroscopically distinct binding mechanisms. In the presence of DAPI, (ATT)(6) forms a monomeric hairpin structure stabilized by two ligands located in the minor groove with a strong apparent binding constant of 3.4 x 10(6) M-1. The DAPI-induced (ATT)(6) hairpin is characterized by well-stacked A.T Watson-Crick and T.T wobble base pairs, a high electrophoretic mobility, and a melting temperature of 41 degrees C. Interaction of DAPI with the complementary (AAT)(6) strand favors less stable base-paired structures, and the results are consistent with electrostatic and hydrogen-bond interactions of the ligand with the phosphodiester backbone of (AAT)(6) by minor involvement of DNA bases.
2000
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/10 - BIOCHIMICA
English
Con Impact Factor ISI
REPLICATION IN-VITRO; 4',6-DIAMIDINO-2-PHENYLINDOLE DAPI; TRIPLET REPEATS; HUMAN-DISEASE; MOLECULAR-DYNAMICS; CATALYTIC ACTIVITY; DNA INTERACTIONS; SITES; INTERCALATION; MISMATCHES
Trotta, E., Del Grosso, N., Erba, M., Paci, M. (2000). The ATT strand of AAT center dot ATT trinucleotide repeats adopts stable hairpin structures induced by minor groove binding ligands. BIOCHEMISTRY, 39(23), 6799-6808 [10.1021/bi0001473].
Trotta, E; Del Grosso, N; Erba, M; Paci, M
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/44475
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact