1983
DOI: 10.1016/0301-4622(83)87015-x
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The interactions between nucleic acids and polyamines

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Cited by 60 publications
(16 citation statements)
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“…[151]) by 13 C NMR [155], for spermine (10) and spermidine (11) by 1 H [156] and 13 C NMR [153,154], for thermospermine by 15 N NMR [157] and for the neuroactive wasp toxin philanthotoxin-343 by 1 H and 13 C NMR titration [158]. Microconstants have been determined by NMR titration for N-(2-mercaptoethyl)-1,3-diaminopropane [159], tetren [27], spermine, spermidine, and homologues [154,160].…”
Section: Open-chain Polyaminesmentioning
confidence: 99%
“…[151]) by 13 C NMR [155], for spermine (10) and spermidine (11) by 1 H [156] and 13 C NMR [153,154], for thermospermine by 15 N NMR [157] and for the neuroactive wasp toxin philanthotoxin-343 by 1 H and 13 C NMR titration [158]. Microconstants have been determined by NMR titration for N-(2-mercaptoethyl)-1,3-diaminopropane [159], tetren [27], spermine, spermidine, and homologues [154,160].…”
Section: Open-chain Polyaminesmentioning
confidence: 99%
“…Among these polyamines, spermine is reported to possess the highest biological activity 10 . Under physiologic ionic and pH conditions, polyamines are multivalent cations with aliphatic hydrocarbon chains separating the charges 11 , and hence negatively charged nucleic acids, including DNA and RNA, are their prime targets of interaction, and consequently regulate the structures of DNA, condense DNA molecules to a liquid crystalline phase 12 , and enhance the activity of G-quadruplex/hemin DNAzymes in vitro 13 . Many evidences suggest that polyamines play important roles as modulators of nucleic acid structure 14 .…”
Section: Introductionmentioning
confidence: 99%
“…Taking these works together, it appears likely that the predominant conformations of polyamines depend upon a balance between stabilizing intramolecular H-bonds and minimization of repulsive steric and electrostatic interactions and that these are strongly influenced by the nature and pH of the medium ( 2 ). Titration studies monitoring pKa's of spermine and spermidine suggest at physiological pH all polyamine nitrogens are probably mainly in the protonated state, which is likely significant not only for their conformation but also their properties in cells ( 6 , 7 ).…”
Section: Introductionmentioning
confidence: 99%