Naturally occurring branched-chain polyamines induce a crosslinked meshwork structure in a giant DNA
Author(s) -
Akira Muramatsu,
Yuta Shimizu,
Yuko Yoshikawa,
Wakao Fukuda,
Naoki Umezawa,
Yuhei Horai,
Tsunehiko Higuchi,
Shinsuke Fujiwara,
Tadayuki Imanaka,
Kenichi Yoshikawa
Publication year - 2016
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.4972066
Subject(s) - dna , polyamine , chemistry , circular dichroism , biophysics , molecule , folding (dsp implementation) , chain (unit) , crystallography , biochemistry , stereochemistry , biology , organic chemistry , physics , astronomy , electrical engineering , engineering
We studied the effect of branched-chain polyamines on the folding transition of genome-sized DNA molecules in aqueous solution by the use of single-molecule observation with fluorescence microcopy. Detailed morphological features of polyamine/DNA complexes were characterized by atomic force microscopy (AFM). The AFM observations indicated that branched-chain polyamines tend to induce a characteristic change in the higher-order structure of DNA by forming bridges or crosslinks between the segments of a DNA molecule. In contrast, natural linear-chain polyamines cause a parallel alignment between DNA segments. Circular dichroism measurements revealed that branched-chain polyamines induce the A-form in the secondary structure of DNA, while linear-chain polyamines have only a minimum effect. This large difference in the effects of branched- and linear-chain polyamines is discussed in relation to the difference in the manner of binding of these polyamines to negatively charged double-stranded DNA.
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