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PMID: 896472 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Carbodiimide modification of superhelical PM2 DNA: considerations regarding reaction at unpaired bases and the unwinding of superhelical DNA with chemical probes.

Nucleic acids research ·Vol. 4 ·No. 6 ·1977-06-00 ·Pages 1695-711

Lebowitz J, Chaudhuri AK, Gonenne A, Kitos G

Abstract

Superhelical PM2 DNA I can be modified with N-cyclohexyl-N'-beta-(4-methylmorpholinium)ethyl carbodiimide (CMC). The transition of the sedimentation coefficient uncorrected for buoyant density change (S20,*) vs. % reactivity in terms of base pairs shows the following characteristics. The S20,* increases by 4.5 S units upon 1% modification. There is a plateau in S20,* between 1 and 4% reactivity. The extent of reactivity was determined by buoyant density and 14C radioactive CMC binding measurements. Further reactivity was not explored since Pulleyblank and Morgan's (22) data of S20,* vs. % reactivity from 6 to 34% was previously published. The initial results obtained in this study are complementary to the cited results of the above authors. Consequently, both sets of data taken together represent a complete description of S20,* vs. % reactivity with CMC. It is shown that the model in which superhelical DNA is proposed to contain small intrastrand hairpin regions can be extended to account for the observed transitions in S20,* vs. reactivity.

MeSH Terms
Carbodiimides/pharmacology Centrifugation, Density Gradient DNA, Viral Morpholines/pharmacology Nucleic Acid Conformation/drug effects Temperature Ultracentrifugation
Chemicals
Carbodiimides DNA, Viral Morpholines
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lebowitz J
Chaudhuri A K
Gonenne A
Kitos G
References (27)
27 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1977-06-00
Pages
1695-711
Language
English
Region
England
NLM ID
0411011
PMCID
PMC342515
Subset
IM
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