Literature DB >> 11072829

Sequence-dependent bending of DNA induced by cisplatin: NMR structures of an A.T-rich 14-mer duplex.

J A Parkinson1, Y Chen, P del Socorro Murdoch, Z Guo, S J Berners-Price, T Brown, P J Sadler.   

Abstract

The NMR solution structure of the A.T rich DNA 14-mer duplex d(ATACATGGTACATA).d(TATGTACCATGTAT) is reported. This is compared with the NMR structure of the same duplex intrastrand cross-linked at the d(G*pG*) site by cis-(Pt(NH3)2¿2+, derived from the anticancer drug cisplatin. The unmodified duplex has B-DNA geometry, but there is a large positive base-pair roll (roll angle 24 +/- 2 degrees) at the T9-A10 step on the 3' side of the central GG site. Platination of the DNA duplex causes the adjacent guanine bases to roll toward one another (roll angle 44 +/- 4 degrees), leading to an overall helix bend of 52 +/- 9 degrees. The platinum atom is displaced from the planes of the coordinated G7* and G8* by 0.8 A and 0.3 A, respectively. The minor groove opposite the platinum lesion is widened and flattened, with geometric parameters similar to those of A-form DNA. The unwinding of the helix at the platination site is 26 degrees. Platination causes the DNA duplex to bend toward the 3'-end (with respect to the G*G* strand), in contrast to G C-rich structures reported previously, which bend toward the 5'-end. This difference can be attributed to the predisposition of the A.T rich duplex toward bending in this region. Protein recognition of bent platinated G*G* lesions may therefore exhibit a strong dependence on the local DNA structure.

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Year:  2000        PMID: 11072829     DOI: 10.1002/1521-3765(20001002)6:19<3636::aid-chem3636>3.3.co;2-n

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Competitive formation of DNA linkage isomers by a trinuclear platinum complex and the influence of pre-association.

Authors:  Joseph J Moniodis; Donald S Thomas; Murray S Davies; Susan J Berners-Price; Nicholas P Farrell
Journal:  Dalton Trans       Date:  2015-02-28       Impact factor: 4.390

2.  Sequence-specific recognition of cancer drug-DNA adducts by HMGB1a repair protein.

Authors:  Robert M Elder; Arthi Jayaraman
Journal:  Biophys J       Date:  2012-05-15       Impact factor: 4.033

  2 in total

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