The interaction between calf thymus DNA （ctDNA） and Pd （Ⅱ） meso-tetralds- （4-N-methyl pyridiniumyl） porphyrin （Pd-TMPyP） was investigated by steady solid-substrate room temperature phosphorescence （SS-RTP）....The interaction between calf thymus DNA （ctDNA） and Pd （Ⅱ） meso-tetralds- （4-N-methyl pyridiniumyl） porphyrin （Pd-TMPyP） was investigated by steady solid-substrate room temperature phosphorescence （SS-RTP）. The SS-RTP intensity and lifetime of Pd-TMPyP enhanced with the increasing ctDNA. The anion quenching experiment of Pd-TMPyP indicated that Pd-TMPyP intercalated into ctDNA, which was also approved by UV-Vis spectra. Keywords： Pd-TMPyP, ctDNA, SS-RTP, intercalation展开更多
The binding properties between meso-tetrakis(4-(N-methylpyridiumyl))porphyrin (TMPyP4) and the parallel DNA G-quadruplex (G4) of telomeric repeated sequence 5′-TTAGGG-3′ have been characterized by means of circular ...The binding properties between meso-tetrakis(4-(N-methylpyridiumyl))porphyrin (TMPyP4) and the parallel DNA G-quadruplex (G4) of telomeric repeated sequence 5′-TTAGGG-3′ have been characterized by means of circular dichroism,steady-state absorption,steady-state fluorescence and picosecond time-resolved fluorescence spectroscopies. The binding constant and the saturated binding number were determined as 1.29×106 (mol/L)-1 and 3,respectively,according to steady-state absorption spec-troscopy. Based on the findings by the use of time-resolved fluorescence spectroscopic technique,it is deduced that TMPyP4 binds to a DNA G-quadruplex with both the thread-intercalating and end-stacking modes and at the saturated binding state,one TMPyP4 molecule intercalates into the intervals of G-tetrads while the other two stack to the ends of the DNA G-quadruplex.展开更多
It is known that at low concentrations of TMPyP4, this porphyrin predominantly intercalates between GC pairs at GC-rich sites of duplex DNA and G-quadruplexes of various constructions, and stabilizes these structures....It is known that at low concentrations of TMPyP4, this porphyrin predominantly intercalates between GC pairs at GC-rich sites of duplex DNA and G-quadruplexes of various constructions, and stabilizes these structures. However, there are still some arguable suggestions about the exact binding sites and modes of TMPyP4 to GC-rich regions of DNA in case of helation of divalent ions with help of the porphrin, which makes porphyrin structure asymmetric. We examined TOEPyP4—analogue of TMPyP4—and studied interaction of TOEPyP4 into the calf thymus DNA at presence of nanomole concentrations of one of the most important microelements in cell vital function—Zn ion. On the basis of CD and absorption spectra of the DNA-TOEPyP4 mixture, it was determined that nanomole concentrations of Zn ions changed porphyrin intercalative binding mode to some external binding modes, which initiated transition of the canonic B conformation of DNA into C-like conformation, and incubation of the (DNA-TOEP4) + Zn mixture at 37?C caused B-Z-like transition, but no transition was observed for the DNA-TOEPyP4 mixture. In particular, at 10 mM?NaCl, TOEPyP4/DNA = 0.02, the binding mode change was observed in the concentration range from 150 to 300 nM?Zn, and the B-C-like transition occurred from 150 to 600 nM?Zn. The B-Z transition at TOEPyP4/DNA = 0.015, Zn/DNA = 0.015, NaCI 10 mM, T = 37?C was observed within incubation time interval from 0.3 to 20 hours, and maximal percent of Z-like form was seen when incubation time interval was from 5 to 6 hours.展开更多
The effect of various metal ions on the DNA mediated energy transfer between simultaneously bound drugs was investigated using spectroscopic methods.It was found that addition of divalent metal ions(Mg^(2+),Ca^(2+),Mn...The effect of various metal ions on the DNA mediated energy transfer between simultaneously bound drugs was investigated using spectroscopic methods.It was found that addition of divalent metal ions(Mg^(2+),Ca^(2+),Mn^(2+),Co^(2+)and Ni^(2+))resulted in further decrease of the ethidium fluorescence intensity,while a small increase was observed in the TMPyP emission band,implying that the energy of excited ethidium was transferred to TMPyP.This DNA-mediated quenching efficiency between ethidium and TMPyP was significantly enhanced by the presence of all metal ions.Among the divalent metal ions,alkali earth metal ions and Mn^(2+)displayed higher quenching efficiencies than other transition metal ions.The distances required to permit the energy transfer between the two drugs in DNA were calculated as 68,66,62,48and 38in the presence of100μmol·L^(-1 )of Mg^(2+),Ca^(2+),Mn^(2+),Co^(2+)and Ni ^(2+)ion,respectively.The disturbed binding conformation of TMPyP in DNA by metal ions presumably accounts for the difference.展开更多
The study of the electrochemical behavior of water soluble porphyrins and metalloporphyrins is interesting and important in the fields of chemistry and biology. For instance, some metalloporphyrins are the catalysts o...The study of the electrochemical behavior of water soluble porphyrins and metalloporphyrins is interesting and important in the fields of chemistry and biology. For instance, some metalloporphyrins are the catalysts of redox reactions in chlorophyll. A previous paper reported the electrochemical properties of Zn-TPPS. This note discusses the voltammetric behavior of TMPyP and Zn-TMPyP.展开更多
基金the National Natural Science Foundation of China （No.20275022）.
文摘The interaction between calf thymus DNA （ctDNA） and Pd （Ⅱ） meso-tetralds- （4-N-methyl pyridiniumyl） porphyrin （Pd-TMPyP） was investigated by steady solid-substrate room temperature phosphorescence （SS-RTP）. The SS-RTP intensity and lifetime of Pd-TMPyP enhanced with the increasing ctDNA. The anion quenching experiment of Pd-TMPyP indicated that Pd-TMPyP intercalated into ctDNA, which was also approved by UV-Vis spectra. Keywords： Pd-TMPyP, ctDNA, SS-RTP, intercalation
基金the National Natural Science Foundation of China (Grant Nos. 20442004, 10576002 and 20703067)
文摘The binding properties between meso-tetrakis(4-(N-methylpyridiumyl))porphyrin (TMPyP4) and the parallel DNA G-quadruplex (G4) of telomeric repeated sequence 5′-TTAGGG-3′ have been characterized by means of circular dichroism,steady-state absorption,steady-state fluorescence and picosecond time-resolved fluorescence spectroscopies. The binding constant and the saturated binding number were determined as 1.29×106 (mol/L)-1 and 3,respectively,according to steady-state absorption spec-troscopy. Based on the findings by the use of time-resolved fluorescence spectroscopic technique,it is deduced that TMPyP4 binds to a DNA G-quadruplex with both the thread-intercalating and end-stacking modes and at the saturated binding state,one TMPyP4 molecule intercalates into the intervals of G-tetrads while the other two stack to the ends of the DNA G-quadruplex.
文摘It is known that at low concentrations of TMPyP4, this porphyrin predominantly intercalates between GC pairs at GC-rich sites of duplex DNA and G-quadruplexes of various constructions, and stabilizes these structures. However, there are still some arguable suggestions about the exact binding sites and modes of TMPyP4 to GC-rich regions of DNA in case of helation of divalent ions with help of the porphrin, which makes porphyrin structure asymmetric. We examined TOEPyP4—analogue of TMPyP4—and studied interaction of TOEPyP4 into the calf thymus DNA at presence of nanomole concentrations of one of the most important microelements in cell vital function—Zn ion. On the basis of CD and absorption spectra of the DNA-TOEPyP4 mixture, it was determined that nanomole concentrations of Zn ions changed porphyrin intercalative binding mode to some external binding modes, which initiated transition of the canonic B conformation of DNA into C-like conformation, and incubation of the (DNA-TOEP4) + Zn mixture at 37?C caused B-Z-like transition, but no transition was observed for the DNA-TOEPyP4 mixture. In particular, at 10 mM?NaCl, TOEPyP4/DNA = 0.02, the binding mode change was observed in the concentration range from 150 to 300 nM?Zn, and the B-C-like transition occurred from 150 to 600 nM?Zn. The B-Z transition at TOEPyP4/DNA = 0.015, Zn/DNA = 0.015, NaCI 10 mM, T = 37?C was observed within incubation time interval from 0.3 to 20 hours, and maximal percent of Z-like form was seen when incubation time interval was from 5 to 6 hours.
基金the National Research Foundation of Korea(20011-0013534,2009-0076930) the National Natural Science Foundation of China(21265022)
文摘The effect of various metal ions on the DNA mediated energy transfer between simultaneously bound drugs was investigated using spectroscopic methods.It was found that addition of divalent metal ions(Mg^(2+),Ca^(2+),Mn^(2+),Co^(2+)and Ni^(2+))resulted in further decrease of the ethidium fluorescence intensity,while a small increase was observed in the TMPyP emission band,implying that the energy of excited ethidium was transferred to TMPyP.This DNA-mediated quenching efficiency between ethidium and TMPyP was significantly enhanced by the presence of all metal ions.Among the divalent metal ions,alkali earth metal ions and Mn^(2+)displayed higher quenching efficiencies than other transition metal ions.The distances required to permit the energy transfer between the two drugs in DNA were calculated as 68,66,62,48and 38in the presence of100μmol·L^(-1 )of Mg^(2+),Ca^(2+),Mn^(2+),Co^(2+)and Ni ^(2+)ion,respectively.The disturbed binding conformation of TMPyP in DNA by metal ions presumably accounts for the difference.
基金Project supported by the National Natural Science Foundation of China.
文摘The study of the electrochemical behavior of water soluble porphyrins and metalloporphyrins is interesting and important in the fields of chemistry and biology. For instance, some metalloporphyrins are the catalysts of redox reactions in chlorophyll. A previous paper reported the electrochemical properties of Zn-TPPS. This note discusses the voltammetric behavior of TMPyP and Zn-TMPyP.
