The enzyme mechanism of nitrite reductase studied at single-molecule level.

نویسندگان

  • Sofya Kuznetsova
  • Gerhild Zauner
  • Thijs J Aartsma
  • Hans Engelkamp
  • Nikos Hatzakis
  • Alan E Rowan
  • Roeland J M Nolte
  • Peter C M Christianen
  • Gerard W Canters
چکیده

A generic method is described for the fluorescence "readout" of the activity of single redox enzyme molecules based on Förster resonance energy transfer from a fluorescent label to the enzyme cofactor. The method is applied to the study of copper-containing nitrite reductase from Alcaligenes faecalis S-6 immobilized on a glass surface. The parameters extracted from the single-molecule fluorescence time traces can be connected to and agree with the macroscopic ensemble averaged kinetic constants. The rates of the electron transfer from the type 1 to the type 2 center and back during turnover exhibit a distribution related to disorder in the catalytic site. The described approach opens the door to single-molecule mechanistic studies of a wide range of redox enzymes and the precise investigation of their internal workings.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 105 9  شماره 

صفحات  -

تاریخ انتشار 2008