4BZU

The Solution Structure of the MLN 944-d(TATGCATA)2 Complex

Summary for 4BZU

• Entry DOI: 10.2210/pdb4bzu/pdb
• Related: 4BZT 4BZV
• Descriptor: DNA, 1-METHYL-9-[12-(9-METHYLPHENAZIN-10-IUM-1-YL)-12-OXO-2,11-DIAZA-5,8-DIAZONIADODEC-1-ANOYL]PHENAZIN-10-IUM (2 entities in total)
• Functional Keywords: bis(phenazine-1-carboxamides), mln 944, dna, intercalation, drug design, anticancer drug.
• Biological source: SYNTHETIC CONSTRUCT
• Total number of polymer chains: 2
• Total formula weight: 5441.98

Authors

Serobian, A.,Thomas, D.S.,Ball, G.E.,Denny, W.A.,Wakelin, L.P.G. (deposition date: 2013-07-30, release date: 2013-08-21, Last modification date: 2024-05-15)

Primary citation

Serobian, A.,Thomas, D.S.,Ball, G.E.,Denny, W.A.,Wakelin, L.P.G.
The Solution Structure of Bis(Phenazine-1-Carboxamide)-DNA Complexes: Mln 944 Binding Corrected and Extended.
Biopolymers, 101:1099-, 2014

PubMed Abstract: MLN 944 is a bisintercalating DNA-binding antitumor agent known to be a template inhibitor of transcription. Previous (1) H NMR studies of its d(ATGCAT)2 complex concluded that its phenazine chromophores are protonated. However, we find that this is not so, which has important consequences for the charged state of the ligand, for the orientation of its 1-carboxamide group in the complex, and for the details of the interaction of its protonated interchromophore linker with the DNA base pairs. Here, we report a corrected solution structure of the MLN 944-d(ATGCAT)2 complex, and extend the study to complexes with d(TATGCATA)2 , and d(TACGCGTA)2 , using a variety of (1) H and (31) P NMR methods and molecular dynamics simulations employing the AMBER 12 force field. We find that for all three complexes MLN 944 binds as a dication, in which the chromophores are uncharged, in the DNA major groove spanning the central 2 GC base pairs in a manner that maintains the dyad symmetry of the DNA. The carboxamide group lies in the plane of the chromophore, its NH making hydrogen bonding interactions with the phenazine N10 nitrogen, and the protonated linkers form hydrogen bonds with the O6 atom of guanine. The dynamics simulations reveal extensive solvent interactions involving the linker amines, the carboxamide group, and the DNA bases.

PubMed: 24898663
DOI: 10.1002/BIP.22513

Experimental method

SOLUTION NMR