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Kinetic Analysis of the Reaction Between d(TTGGCCAA) and [Pt(NH3)3(H2O)]2+ by Enzymatic Degradation of the Products and ESI and MALDI Mass Spectrometries

✍ Scribed by Gonnet, F.; Kocher, F.; Blais, J. C.; Bolbach, G.; Tabet, J. C.; Chottard, J. C.


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
666 KB
Volume
31
Category
Article
ISSN
1076-5174

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✦ Synopsis


The kinetics of the reaction between the octanucleotide d(TTGGCCAA) in the single-stranded form in pure water and the platinum complex [ Pt(NH,),(H,O)] 2+ was investigated by electrospray ionization and matrix-assisted laser desorption/ionization (MALDI) mass spectrometries coupled with enzymatic degradation of the adducts. These methods led to the determination of specific rate constants of platination. The global rate constant characteristic of the formation of adducts on each 5'or 3'-guanine were measured by electrospray ionization analysis. The ratios between the 5'-and 3'-adducts were determined from enzymatic degradation of the final reaction mixture and MALDI analysis. The platination in water is approximately eight times faster than in 0.1 M NaCIO,. The selectivity of platination is a factor of 2 in favor of the 5'-guanine, and similar to that observed for the reaction between d(CTGGCTCA) and [Pt(NH3)3(H20)] '+ in 0.1 M NaCIO,.


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Solvent and salt effects on the kinetics
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## Abstract The kinetics of replacement of H~2~O by [Ru(NH~3~)pz]^2+^ (pz = pyrazine) in [Fe(CN)~5~H~2~O]^3βˆ’^ have been studied in various concentrated electrolyte solutions and in various water–cosolvent mixtures, at 298 K. Salt and cosolvent effects can be rationalized taking into account specifi