Detecting Vibrational Energy Transfer into an Enzyme Active Site via a Transition State Analog
High Resolution Image Download MS PowerPoint Slide Vibrational energy transfer (VET) in enzymes has been discussed in the context of enzyme catalysis. A key point for experimentally investigating VET is to position suitable vibrational energy sensors in the delicate active sites of enzymes without disturbing their native state. Ideally, native substrates and/or inhibitors can be repurposed as vibrational energy sensors. Here, we demonstrate that the azide anion (N 3 – ), bound as an inhibitor to the active site of formate dehydrogenase (FDH), sensitively detects the vibrational energy, even though it is not covalently bound. Vibrational energy has been site-specifically injected into the enzyme via exciting an azulenylalanine (AzAla) energy donor, which has been introduced by genetic code expansion in a 19 Å distance. This proof-of-principle experiment opens the field toward the investigation of VET on a picosecond time scale in a range of enzymes by exploiting their natural affinity toward the infrared-absorbing small ligand azide.
Authors
- Erhan Deniz (ORCID: https://orcid.org/0000-0002-6890-2989)
- Carolin Feid (ORCID: https://orcid.org/0000-0003-2534-2130)
- Jan G. Löffler (ORCID: https://orcid.org/0000-0003-4085-592X)
- Jens Bredenbeck (ORCID: https://orcid.org/0000-0003-1929-9092)
- Yunxia Shen
Institutions
- Goethe University Frankfurt (DE)
Publication Details
- Journal
- The Journal of Physical Chemistry Letters
- Published
- 2026-06-26
- DOI
- https://doi.org/10.1021/acs.jpclett.6c01422
- Primary Topic
- Spectroscopy and Quantum Chemical Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Stiftung Polytechnische Gesellschaft Frankfurt am Main
- California Institute of Technology
- Deutsche Forschungsgemeinschaft
- RIKEN