J 2002

Biophysical analysis of natural, double-helical DNA modified by a dinuclear platinum(II) organometallic compound in a cell-free medium

MARINI, Victoria, Jana KAŠPÁRKOVÁ, Olga NOVAKOVA, Luigi MONSU SCOLARO, Raffaello ROMEO et. al.

Základní údaje

Originální název

Biophysical analysis of natural, double-helical DNA modified by a dinuclear platinum(II) organometallic compound in a cell-free medium

Název česky

Biofyzikální analýza dvouřetězcová DNA modifikována dinukleární platinovou organometalovou sloučeninou

Autoři

MARINI, Victoria (858 Uruguay), Jana KAŠPÁRKOVÁ (203 Česká republika), Olga NOVAKOVA (203 Česká republika), Luigi MONSU SCOLARO (380 Itálie), Raffaello ROMEO (380 Itálie) a Viktor BRABEC (203 Česká republika, garant)

Vydání

Journal of Biological Inorganic Chemistry, 2002, 0949-8257

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10610 Biophysics

Stát vydavatele

Německo

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 3.911

Kód RIV

RIV/00216224:14310/02:00028886

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

DNA;Organoplatinum(II);Adducts;Cross-link;Conformation
Změněno: 20. 6. 2009 16:08, Mgr. María Victoria Marini Palomeque, Ph.D.

Anotace

V originále

Modifications of natural DNA by the dinuclear platinum(II) organometallic complex [{Pt(Me)Cl(Me2SO)}2(-N-N)] [where N-N=H2N(CH2)6NH2] (ORGANObisPt) were studied by methods of molecular biophysics. These methods include DNA binding studies using atomic absorption spectrophotometry, HPLC analysis of enzymatically digested DNA, interstrand cross-linking employing gel electrophoresis under denaturing conditions, DNA unwinding studied by gel electrophoresis, mapping of DNA adducts by transcription assay, DNA melting curves measured by absorption spectrophotometry and conformational analysis of platinated DNA by differential pulse polarography. The results indicate that the complex ORGANObisPt binds irreversibly to DNA. Its DNA binding mode is, however, different from that of the formally equivalent [{cis-PtCl(NH3)2}2(-N-N)] (1,1/c,c), which exhibits antitumor activity including that in the tumor cells resistant to cisplatin. Interestingly, ORGANObisPt binds to DNA considerably faster than 1,1/c,c and cisplatin. In addition, when ORGANObisPt binds to DNA it exhibits a strong base sequence specificity to guanine residues. ORGANObisPt forms mainly monofunctional adducts on double-helical DNA. It forms also a small amount of DNA interstrand cross-links (~2%), i.e. a radically smaller amount in comparison with the complex 1,1/c,c. Importantly, these interstrand cross-links of ORGANObisPt are capable of terminating RNA synthesis in vitro, while its major monofunctional adducts are not. In addition, the adducts of ORGANObisPt affect the conformation of DNA, but in a different way than its dinuclear analogue 1,1/c,c or cisplatin. Some structural features of ORGANObisPt, such as the charge or nature of the trans and cis activating groups relative to the labile chloride, might be responsible for the altered DNA binding mode and biological activity in comparison with the 1,1/c,c compound.

Česky

Modifikace DNA dinukleárním platinovým (II) organometalickým komplexem [{Pt(Me)Cl(Me2SO)}2(-N-N)] [kde N-N=H2N(CH2)6NH2] (ORGANObisPt) byly studovány metody molekulární biofyziky.

Návaznosti

GA301/00/0556, projekt VaV
Název: Dvojjaderné komplexy kovů jako agens schopná vytvářet můstky mezi DNA a bílkovinami
GA305/02/1552, projekt VaV
Název: Oligonukleotidy modifikované komplexy platiny pro selektivní modulaci genové exprese; vztah k "protismyslné" strategii při vývoji nových farmak.