Sequence preference of chloroquine binding to DNA and prevention of Z-DNA formation.

Abstract:

:Chloroquine is a critically important antimalarial drug and a well known intercalator into DNA. We now show that chloroquine binds more avidly to poly(dG-dC).poly(dG-dC) than to other synthetic polynucleotides and that this binding inhibits both salt- and cobalt-induced transitions to Z-DNA. These data are consistent with the possibility that chloroquine's toxicity to malarial parasites is mediated by its effect on DNA.

journal_name

Mol Biochem Parasitol

authors

Kwakye-Berko F,Meshnick S

doi

10.1016/0166-6851(90)90066-u

subject

Has Abstract

pub_date

1990-03-01 00:00:00

pages

275-8

issue

2

eissn

0166-6851

issn

1872-9428

pii

0166-6851(90)90066-U

journal_volume

39

pub_type

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