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A homogeneous type II DNA topoisomerase from HeLa cell nuclei.

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Miller, K G, Liu, L F, Englund, P T·1981·Journal of Biological Chemistry

Abstract

Using kinetoplast DNA networks as a substrate in a decatenation assay, we have purified to apparent homogeneity a type II DNA topoisomerase from HeLa cell nuclei. The most pure preparations contain a single polypeptide of 172,000 daltons as determined by sodium dodecyl sulfate-gel electrophoresis. The molecular weight of the native protein, based on sedimentation and gel filtration analyses, is estimated to be 309,000. These results suggest that the enzyme is a dimer of 172,0090-dalton subunits. The enzyme is a type II topoisomerase as demonstrated by its ability to change the linking number of DNA circles in steps of two and to decatenate or unknot covalently closed DNA circles. No gyrase activity is detectable. ATP is required for the relaxation, decatenation, and unknotting of DNA, and a DNA-dependent ATPase activity is present in the most pure fractions. ATP is hydrolyzed to ADP in this properties to T4 DNA topoisomerase (Liu, L. F., Liu, C. C., and Alberts, B. M. (1979) Nature 281, 456-461).

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Metadata

Authors
Miller, K. G., Liu, L. F., & Englund, P. T.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1981-09
Volume
256
Issue
17
Pages
9334-9339
ISSN
0021-9258 (ISSN-L)
OpenAlex
W1566761847
Cited by
356
References
0
FWCI
7.95
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: A homogeneous type II DNA topoisomerase from HeLa cell nuclei. https://app.cochat.ai/papers/10.1016/s0021-9258(19)52552-2
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Miller, K. G., Liu, L. F., & Englund, P. T. (1981). A homogeneous type II DNA topoisomerase from HeLa cell nuclei. Journal of Biological Chemistry. https://doi.org/10.1016/s0021-9258(19)52552-2

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