DNA interaction with complex ions in solution

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DNA interaction with complex ions in solution. / Kasyanenko, N. A.; Zanina, A. V.; Nazarova, O. V.; Panarin, E. F.

In: Langmuir, Vol. 15, No. 23, 09.11.1999, p. 7912-7917.

Research output: Contribution to journal › Article › peer-review

Harvard

Kasyanenko, NA, Zanina, AV, Nazarova, OV & Panarin, EF 1999, 'DNA interaction with complex ions in solution', Langmuir, vol. 15, no. 23, pp. 7912-7917. https://doi.org/10.1021/la980980p

APA

Kasyanenko, N. A., Zanina, A. V., Nazarova, O. V., & Panarin, E. F. (1999). DNA interaction with complex ions in solution. Langmuir, 15(23), 7912-7917. https://doi.org/10.1021/la980980p

Vancouver

Kasyanenko NA, Zanina AV, Nazarova OV, Panarin EF. DNA interaction with complex ions in solution. Langmuir. 1999 Nov 9;15(23):7912-7917. https://doi.org/10.1021/la980980p

Author

Kasyanenko, N. A. ; Zanina, A. V. ; Nazarova, O. V. ; Panarin, E. F. / DNA interaction with complex ions in solution. In: Langmuir. 1999 ; Vol. 15, No. 23. pp. 7912-7917.

BibTeX

@article{0d8c30d392e14c37bc236758eb89949e,

title = "DNA interaction with complex ions in solution",

abstract = "The methods of flow birefringence, low shear viscometry, and circular dichroism were used to investigate the DNA conformation in solution during the interaction with coordination compounds [Co(NH3)6]Cl3 and [Co(NO2)6]Na3. It has been shown that the compound [Co(NO2)6]Na3, which dissociates in an aqueous solution to produce a negative complex ion [Co(NO2)6]3-, binds to a DNA molecule, causing considerable changes in its parameters. For the binding to occur, the complex ion must undergo a transition to its aqueous form. Even a low cobalt content is shown to produce DNA shrinkage. It is attended by an increased DNA optical anisotropy. This effect was observed for both compounds used. The comparison of these data with earlier results on DNA-Fe3+ interaction has revealed some features common to the DNA binding to trivalent metal ions. We have suggested that the mutual orientation of DNA statistical segments is changed because of the formation of intramolecular linkages between trivalent ions and remote DNA chain segments.",

keywords = "CONDENSATION, CATIONS, BINDING, CO(III)",

author = "Kasyanenko, {N. A.} and Zanina, {A. V.} and Nazarova, {O. V.} and Panarin, {E. F.}",

year = "1999",

month = nov,

day = "9",

doi = "10.1021/la980980p",

language = "English",

volume = "15",

pages = "7912--7917",

journal = "Langmuir",

issn = "0743-7463",

publisher = "American Chemical Society",

number = "23",

}

RIS

TY - JOUR

T1 - DNA interaction with complex ions in solution

AU - Kasyanenko, N. A.

AU - Zanina, A. V.

AU - Nazarova, O. V.

AU - Panarin, E. F.

PY - 1999/11/9

Y1 - 1999/11/9

N2 - The methods of flow birefringence, low shear viscometry, and circular dichroism were used to investigate the DNA conformation in solution during the interaction with coordination compounds [Co(NH3)6]Cl3 and [Co(NO2)6]Na3. It has been shown that the compound [Co(NO2)6]Na3, which dissociates in an aqueous solution to produce a negative complex ion [Co(NO2)6]3-, binds to a DNA molecule, causing considerable changes in its parameters. For the binding to occur, the complex ion must undergo a transition to its aqueous form. Even a low cobalt content is shown to produce DNA shrinkage. It is attended by an increased DNA optical anisotropy. This effect was observed for both compounds used. The comparison of these data with earlier results on DNA-Fe3+ interaction has revealed some features common to the DNA binding to trivalent metal ions. We have suggested that the mutual orientation of DNA statistical segments is changed because of the formation of intramolecular linkages between trivalent ions and remote DNA chain segments.

AB - The methods of flow birefringence, low shear viscometry, and circular dichroism were used to investigate the DNA conformation in solution during the interaction with coordination compounds [Co(NH3)6]Cl3 and [Co(NO2)6]Na3. It has been shown that the compound [Co(NO2)6]Na3, which dissociates in an aqueous solution to produce a negative complex ion [Co(NO2)6]3-, binds to a DNA molecule, causing considerable changes in its parameters. For the binding to occur, the complex ion must undergo a transition to its aqueous form. Even a low cobalt content is shown to produce DNA shrinkage. It is attended by an increased DNA optical anisotropy. This effect was observed for both compounds used. The comparison of these data with earlier results on DNA-Fe3+ interaction has revealed some features common to the DNA binding to trivalent metal ions. We have suggested that the mutual orientation of DNA statistical segments is changed because of the formation of intramolecular linkages between trivalent ions and remote DNA chain segments.

KW - CONDENSATION

KW - CATIONS

KW - BINDING

KW - CO(III)

UR - http://www.scopus.com/inward/record.url?scp=0033355037&partnerID=8YFLogxK

U2 - 10.1021/la980980p

DO - 10.1021/la980980p

M3 - Article

AN - SCOPUS:0033355037

VL - 15

SP - 7912

EP - 7917

JO - Langmuir

JF - Langmuir

SN - 0743-7463

IS - 23

ER -

ID: 73393035