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 language | English |
|---|---|
| Pages (from-to) | 978-980 |
| Number of pages | 3 |
| Journal | Journal of Synchrotron Radiation |
| Volume | 8 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 1 2001 |
Keywords
- Freeze-quench
- Metalloenzyme
- XAS
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