The blue light photoreceptor YtvA from Bacillus subtilis has an N-terminal flavin mononucleotide (FMN)-binding light, oxygen, voltage (LOV) domain that is fused to a C-terminal sulfate transporter and anti-σ factor antagonist (STAS) output domain. To interrogate the signal transduction pathway that leads to photoactivation, the STAS domain was replaced with a histidine kinase so that photoexcitation of the flavin could be directly correlated with biological activity. N94, a conserved Asn that is hydrogen bonded to the FMN C2=O group, was replaced with Ala, Asp, and Ser residues to explore the role of this residue in triggering the structural dynamics that activate the output domain. Femtosecond to millisecond time-resolved multiple probe spectroscopy (TRMPS) coupled with a fluorescence polarization (FP) assay revealed that the loss of the hydrogen bond between N94 and the C2=O group decoupled changes in protein structure from photoexcitation. In addition, alterations in N94 also decreased the stability of the Cys-FMN adduct formed in the light activated state by up to a factor of ~25. Collectively, these studies shed light on the role of the hydrogen bonding network in the LOV β-scaffold on signal transduction.
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The Photophysical Path to the Triplet State in Light‐Oxygen‐Voltage (LOV) Domains
Abstract Upon blue‐light absorption, LOV domains efficiently undergo intersystem crossing (ISC) to the triplet state. Several factors potentially contribute to this efficiency. One often proposed in the literature is the heavy atom effect of the nearby (and eventually adduct‐forming) cysteine. However, some LOV domain derivatives that lack the cysteine residue also undergo ISC efficiently. Using hybrid multireference quantum mechanical/molecular mechanical (QM / MM) models, we investigated the effect of the electrostatic environment in a prototypal LOV domain,Arabidopsis thalianaPhototropin 1 LOV2 (AtLOV2), compared to the effect of the dielectric of an aqueous solution. We find that the electrostatic environment of AtLOV2 is especially well tuned to stabilize a triplet state, which we posit is the state involved in the ISC step. Other low‐lying triplet states that have and character are ruled out on the basis of energetics and/or their orbital character. The mechanistic picture that emerges from the calculations is one that involves the ISC of photoexcited flavin to a triplet state followed by rapid internal conversion to a triplet state, which is the state detected spectroscopically. This insight into the ISC mechanism can provide guidelines for tuning flavin's photophysics through mutations that alter the protein electrostatic environment and potentially helps to explain why ISC (and subsequent flavin photochemistry) does not occur readily in many classes of flavin‐binding enzymes.
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- Award ID(s):
- 2047667
- PAR ID:
- 10621534
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Chemistry – A European Journal
- Volume:
- 31
- Issue:
- 22
- ISSN:
- 0947-6539
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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