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.

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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

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article

Detecting Vibrational Energy Transfer into an Enzyme Active Site via a Transition State Analog

Erhan Deniz, Carolin Feid, Jan G. Löffler, Jens Bredenbeck et al.
The Journal of Physical Chemistry Letters
Spectroscopy and Quantum Chemical Studies
article

Detecting Vibrational Energy Transfer into an Enzyme Active Site via a Transition State Analog

Erhan Deniz, Carolin Feid, Jan G. Löffler, Jens Bredenbeck, Yunxia Shen
article en

Abstract

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.

The Journal of Physical Chemistry Letters
Goethe University Frankfurt (DE)
Stiftung Polytechnische Gesellschaft Frankfurt am Main, California Institute of Technology, Deutsche Forschungsgemeinschaft, RIKEN
Affordable and clean energy
Openalex Percentile: Top 6%
Spectroscopy and Quantum Chemical Studies
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