Thermodynamics of d(GGGGCCCC) Binding to Neomycin-Class Aminoglycosides.


Journal

Biochemistry
ISSN: 1520-4995
Titre abrégé: Biochemistry
Pays: United States
ID NLM: 0370623

Informations de publication

Date de publication:
06 06 2023
Historique:
medline: 7 6 2023
pubmed: 12 5 2023
entrez: 12 5 2023
Statut: ppublish

Résumé

DNA adopts a number of conformations that can affect its binding to other macromolecules. The conformations (A, B, Z) can be sequence- and/or solution-dependent. While AT-rich DNA sequences generally adopt a Canonical B-form structure, GC-rich sequences are more promiscuous. Recognition of GC-rich nucleic acids by small molecules has been much more challenging than the recognition of AT-rich duplexes. Spectrophotometric and calorimetric techniques were used to characterize the binding of neomycin-class aminoglycosides to a GC-rich DNA duplex, G

Identifiants

pubmed: 37172221
doi: 10.1021/acs.biochem.3c00049
doi:

Substances chimiques

Neomycin I16QD7X297
Aminoglycosides 0
Anti-Bacterial Agents 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1755-1766

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM129325
Pays : United States

Auteurs

Andrea N Conner (AN)

Laboratory for Medicinal Chemistry, Department of Chemistry, Clemson University, Clemson, South Carolina 29634, United States.

Makala T Fuller (MT)

Laboratory for Medicinal Chemistry, Department of Chemistry, Clemson University, Clemson, South Carolina 29634, United States.

Patrick C Kellish (PC)

Laboratory for Medicinal Chemistry, Department of Chemistry, Clemson University, Clemson, South Carolina 29634, United States.

Dev P Arya (DP)

Laboratory for Medicinal Chemistry, Department of Chemistry, Clemson University, Clemson, South Carolina 29634, United States.

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Classifications MeSH