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Time-dependent XAS studies of trapped enzyme-substrate complexes of alcohol dehydrogenase from Thermoanaerobacter brockii

  • Weizmann Institute of Science

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The understanding of structure-function relationships in proteins has been significantly advanced with the advent of the biotechnological revolution. A goal yet to be realized for many metalloenzyme systems is to characterize the dynamic changes in structure that bridge the static endpoints provided by crystallography. We present here a series of edge and EXAFS spectra of the metalloenzyme alcohol dehydrogenase from Thermoanaerobacter brockii (TbADH) complexed with its substrate. The enzyme-substrate complexes were trapped by fast freezing at various times, following their enzyme activity. Our edge and EXAFS analyses both reveal the time-dependent changes in the structure of the active site of TbADH.

Original languageEnglish
Pages (from-to)978-980
Number of pages3
JournalJournal of Synchrotron Radiation
Volume8
Issue number2
DOIs
StatePublished - Mar 1 2001

Keywords

  • Freeze-quench
  • Metalloenzyme
  • XAS

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