Literature DB >> 16491378

Stereoselective and driving-force-dependent photoinduced electron-transfer reactions of zinc myoglobin with optically active N,N'-dimethylcinchoninium and N,N'-dimethylcinchonidinium ions.

Hiroshi Takashima1, Ayako Araki, Keiko Takemoto, Naokazu Yoshikawa, Keiichi Tsukahara.   

Abstract

In order to understand the detailed mechanism of the stereoselective photoinduced electron-transfer (ET) reactions of zinc-substituted myoglobin (ZnMb) with optically active molecules by flash photolysis, we designed and prepared new optically active agents, such as N,N'-dimethylcinchoninium diiodide ([MCN]I2) and N,N'-dimethylcinchonidinium diiodide ([MCD]I2). The photoexcited triplet state of ZnMb, 3(ZnMb)*, was successfully quenched by [MCN]2+ and [MCD]2+ ions to form the radical pair of ZnMb cation (ZnMb.+) and reduced [MCN].+ and [MCD].+, followed by a thermal back ET reaction to the ground state. The rate constants (kq) for the ET quenching at 25 degrees C were obtained as kq(MCN)=(1.9+/-0.1)x10(6) M-1 s-1 and kq(MCD)=(3.0+/-0.2)x10(6) M-1 s-1, respectively. The ratio of kq(MCD)/kq(MCN)=1.6 indicates that the [MCD]2+ preferentially quenches 3ZnMb)*. The second-order rate constants (kb) for the thermal back ET reaction from [MCN].+ and [MCD].+ to ZnMb.+ at 25 degrees C were kb(MCN)=(0.79+/-0.04)x10(8) M-1 s-1 and kb(MCD)=(1.0+/-0.1)x10(8) M-1 s-1, respectively, and the selectivity was kq(MCD)/kq(MCN)=1.3. Both quenching and thermal back ET reactions are controlled by the ET step. In the quenching reaction, the energy differences of DeltaDeltaH ( not equal)(MCD-MCN) and DeltaDeltaS ( not equal)(MCD-MCN) at 25 degrees C were obtained as -1.1 and 0 kJ mol-1, respectively. On the other hand, DeltaDeltaH (not equal)(MCD-MCN)=11+/-2 kJ mol-1 and TDeltaDeltaS (not equal)(MCD-MCN)=-10+/-2 kJ mol-1 were given in the thermal back ET reaction. The highest stereoselectivity of 1.7 for [MCD].+ found at low temperature (10 degrees C) was due to the DeltaDeltaS ( not equal) value obtained in the thermal back ET reaction.

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Year:  2006        PMID: 16491378     DOI: 10.1007/s00775-006-0079-8

Source DB:  PubMed          Journal:  J Biol Inorg Chem        ISSN: 0949-8257            Impact factor:   3.358


  9 in total

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Journal:  Chem Rev       Date:  1996-11-07       Impact factor: 60.622

2.  Migration of small molecules through the structure of hemoglobin: evidence for gating in a protein electron-transfer reaction.

Authors:  J Feitelson; G McLendon
Journal:  Biochemistry       Date:  1991-05-21       Impact factor: 3.162

3.  pH-dependence of photo-induced electron transfer in zinc-substituted sperm whale myoglobin.

Authors:  A C Shosheva; P K Christova; B P Atanasov
Journal:  Biochim Biophys Acta       Date:  1988-11-23

4.  Inhibitor-enhanced electron transfer: copper cytochrome c as a redox-inert probe of ternary complexes.

Authors:  J S Zhou; J M Nocek; M L DeVan; B M Hoffman
Journal:  Science       Date:  1995-07-14       Impact factor: 47.728

5.  Reactions of excited triplet states of metal substituted myoglobin with dioxygen and quinone.

Authors:  S Papp; J M Vanderkooi; C S Owen; G R Holtom; C M Phillips
Journal:  Biophys J       Date:  1990-07       Impact factor: 4.033

6.  Stereoselective Photoinduced Electron-Transfer Reactions of Zinc Myoglobin with Optically Active Viologens.

Authors:  Keiichi Tsukahara; Chieko Kimura; Junko Kaneko; Kaya Abe; Miho Matsui; Tomoko Hara
Journal:  Inorg Chem       Date:  1997-07-30       Impact factor: 5.165

7.  Quenching of the zinc-protoporphyrin triplet state as a measure of small-molecule diffusion through the structure of myoglobin.

Authors:  N Barboy; J Feitelson
Journal:  Biochemistry       Date:  1987-06-02       Impact factor: 3.162

8.  Remarkably stereoselective photoinduced electron-transfer reaction between zinc myoglobin and optically active binaphthyl bisviologen.

Authors:  Hiroshi Takashima; Michiru Tanaka; Yuko Hasegawa; Keiichi Tsukahara
Journal:  J Biol Inorg Chem       Date:  2003-02-15       Impact factor: 3.358

9.  Diffusion of small molecules through the structure of myoglobin. Environmental effects.

Authors:  N Barboy; J Feitelson
Journal:  Biochemistry       Date:  1989-06-27       Impact factor: 3.162

  9 in total
  1 in total

1.  Synthesis and photophysical properties of zinc myoglobin appending an ethidium ion as a DNA intercalator.

Authors:  Hiroshi Takashima; Yukiko Matsushima; Yasuyuki Araki; Osamu Ito; Keiichi Tsukahara
Journal:  J Biol Inorg Chem       Date:  2007-10-18       Impact factor: 3.358

  1 in total

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