کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1318192 | 1499483 | 2006 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Guanine binding of a cytotoxic platinum-acridin-9-ylthiourea conjugate monitored by 1-D 1H and 2-D [1H,15N] NMR spectroscopy: Hydrolysis is not the rate-determining step
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موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی معدنی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Guanine binding of a cytotoxic platinum-acridin-9-ylthiourea conjugate monitored by 1-D 1H and 2-D [1H,15N] NMR spectroscopy: Hydrolysis is not the rate-determining step Guanine binding of a cytotoxic platinum-acridin-9-ylthiourea conjugate monitored by 1-D 1H and 2-D [1H,15N] NMR spectroscopy: Hydrolysis is not the rate-determining step](/preview/png/1318192.png)
چکیده انگلیسی
The reaction of [PtCl(en)(ACRAMTU)](NO3)2 (PT-ACRAMTU, 1; ACRAMTU = 1-[2-(acridin-9-ylamino)ethyl]-1,3-dimethylthiourea, en = ethane-1,2-diamine) and the [15N]-en labeled analogue, 1â², with 2â²-deoxyguanosine (dG) was studied by 1H NMR and two-dimensional [1H,15N] HSQC (heteronuclear single quantum coherence) spectroscopy. Reactions were performed in phosphate buffered solution at 37 °C at various ratios and total concentrations of reactants. The 1H NMR data suggest that the hydrolyzed form of the drug, [Pt(H2O)(en)(ACRAMTU)]3+ (1a), forms at a rate (k1) similar to that observed in classical platinum chloroam(m)ines but to only a minor extent (â¼15%). Attempts to detect and characterize 1â²a by two-dimensional NMR spectroscopy, however, were unsuccessful, and 1â² and dGâ were the only species observed in the HSQC spectra. Reaction of the putative aqua intermediate 1a with dG to yield [Pt(en)(dG-N7)(ACRAMTU)]3+ (dGâ) is slow and is highly dependent on the initial concentrations of the reactants. This unusual observation is consistent with a mechanism in which a second-order term becomes rate-determining (k2 < k1) (the opposite situation is usually observed in cisplatin-type complexes). The possibility of direct substitution of chloride in 1 by dG-N7 (k3) and the implications of the data acquired in this model system for the binding of the conjugate to double-stranded DNA are discussed.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Inorganic Biochemistry - Volume 100, Issues 5â6, May 2006, Pages 972-979
Journal: Journal of Inorganic Biochemistry - Volume 100, Issues 5â6, May 2006, Pages 972-979
نویسندگان
Rajsekhar Guddneppanavar, Marcus W. Wright, Alyssa K. Tomsey, Ulrich Bierbach,