Structures of three classes of anticancer agents bound to the human topoisomerase I-DNA covalent complex.

Article Details

Citation

Staker BL, Feese MD, Cushman M, Pommier Y, Zembower D, Stewart L, Burgin AB

Structures of three classes of anticancer agents bound to the human topoisomerase I-DNA covalent complex.

J Med Chem. 2005 Apr 7;48(7):2336-45.

PubMed ID
15801827 [ View in PubMed
]
Abstract

Human topoisomerase I (top1) is the molecular target of a diverse set of anticancer compounds, including the camptothecins, indolocarbazoles, and indenoisoquinolines. These compounds bind to a transient top1-DNA covalent complex and inhibit the resealing of a single-strand nick that the enzyme creates to relieve superhelical tension in duplex DNA. (Hertzberg, R. P.; et al. Biochem. 1989, 28, 4629-4638. Hsiang, Y. H.; et al. J. Biol. Chem 1985, 260, 14873-14878. Champoux, J. J. Annu. Rev. Biochem. 2001, 70, 369-413. Stewart, L.; et al. Science 1998, 729, 1534-1541.) We report the X-ray crystal structures of the human top1-DNA complex bound with camptothecin and representative members of the indenoisoquinoline and indolocarbazole classes of top1 poisons. The planar nature of all three structurally diverse classes allows them to intercalate between DNA base pairs at the site of single-strand cleavage. All three classes of compounds have a free electron pair near Arg364, a residue that if mutated confers resistance to all three classes of drugs. The common intercalative binding mode is augmented by unexpected chemotype-specific contacts with amino acid residues Asn352 and Glu356, which adopt alternative side-chain conformations to accommodate the bound compounds. These new X-ray structures explain how very different molecules can stabilize top1-DNA covalent complexes and will aid the rational design of completely novel structural classes of anticancer drugs.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
DNA topoisomerase 1P11387Details
Binding Properties
DrugTargetPropertyMeasurementpHTemperature (°C)
CamptothecinDNA topoisomerase 1IC 50 (nM)300N/AN/ADetails
TopotecanDNA topoisomerase 1IC 50 (nM)50N/AN/ADetails