Literature DB >> 15517437

Direct monitoring of the electron pool effect of cytochrome c3 by highly sensitive EQCM measurements.

Noriyuki Asakura1, Toshiaki Kamachi, Ichiro Okura.   

Abstract

Cytochrome c(3) from Desulfovibrio vulgaris has four hemes per molecule, and a redox change at the hemes alters the conformation of the protein, leading to a redox-dependent change in the interaction of cytochrome c(3) with redox partners (an electron acceptor or an electron donor). The redox-dependent change in this interaction was directly monitored by the high-performance electrochemical quartz crystal microbalance (EQCM) technique that has been improved to give high sensitivity in solution. In this method, cytochrome c(3) molecules in solution associate electrostatically with a viologen-immobilized quartz crystal electrode as a monolayer, and redox of the associating cytochrome c(3) is controlled by the immobilized viologen. This technique makes it possible to measure the access of cytochrome c(3) to the electrode or repulsion from the electrode, and hence interconversion between an electrostatic complex and an electron transfer complex on the cytochrome c(3) and the viologen as a mass change accompanying a potential sweep is monitored. In addition, simultaneous measurement of a mass change and a potential step reveals that the cytochrome c(3) stores electrons when the four hemes are reduced (an electron pool effect), that is, the oxidized cytochrome c(3) facilitates acceptance of electrons from the immobilized viologen molecule, but the reduced cytochrome c(3) donates the accepted electrons to the viologen with difficulty.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15517437     DOI: 10.1007/s00775-004-0604-6

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


  22 in total

1.  Application of electrochemical quartz crystal microbalance technique to direct monitoring of cytochrome c3 function as the electron pool during intermolecular electron transfer.

Authors:  Noriyuki Asakura; Toshiaki Kamachi; Ichiro Okura
Journal:  Anal Biochem       Date:  2003-03-01       Impact factor: 3.365

2.  On the anomalous temperature behaviour of the EPR signal of monovalent nickel in hydrogenase.

Authors:  J W Van der Zwaan; S P Albracht; R D Fontijn; P Mul
Journal:  Eur J Biochem       Date:  1987-12-01

3.  Conformational changes in cytochrome c and cytochrome oxidase upon complex formation: a resonance Raman study.

Authors:  P Hildebrandt; T Heimburg; D Marsh; G L Powell
Journal:  Biochemistry       Date:  1990-02-13       Impact factor: 3.162

4.  Spectroscopic analysis of the cytochrome c oxidase-cytochrome c complex: circular dichroism and magnetic circular dichroism measurements reveal change of cytochrome c heme geometry imposed by complex formation.

Authors:  C Weber; B Michel; H R Bosshard
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

5.  Purification and properties of cytochrome c 3 of Desulfovibrio vulgaris, Miyazaki.

Authors:  T Yagi; K Maruyama
Journal:  Biochim Biophys Acta       Date:  1971-08-27

Review 6.  Nickel hydrogenases: in search of the active site.

Authors:  S P Albracht
Journal:  Biochim Biophys Acta       Date:  1994-12-30

7.  Interaction of cytochrome c with the blue copper proteins, plastocyanin and azurin.

Authors:  M A Augustin; S K Chapman; D M Davies; A G Sykes; S H Speck; E Margoliash
Journal:  J Biol Chem       Date:  1983-05-25       Impact factor: 5.157

8.  NMR studies of cooperativity in the tetrahaem cytochrome c3 from Desulfovibrio vulgaris.

Authors:  D L Turner; C A Salgueiro; T Catarino; J Legall; A V Xavier
Journal:  Eur J Biochem       Date:  1996-11-01

9.  Functional and mechanistic studies of cytochrome c3 from Desulfovibrio gigas: thermodynamics of a "proton thruster".

Authors:  R O Louro; T Catarino; D L Turner; M A Piçarra-Pereira; I Pacheco; J LeGall; A V Xavier
Journal:  Biochemistry       Date:  1998-11-10       Impact factor: 3.162

10.  [3Fe-4S] to [4Fe-4S] cluster conversion in Desulfovibrio fructosovorans [NiFe] hydrogenase by site-directed mutagenesis.

Authors:  M Rousset; Y Montet; B Guigliarelli; N Forget; M Asso; P Bertrand; J C Fontecilla-Camps; E C Hatchikian
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-29       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.