Mid-IR quantum cascade laser spectroscopy to resolve lipid dynamics during the photocycle of bacteriorhodopsin
| dc.contributor.author | Stritt, Paul | |
| dc.contributor.author | Jawurek, Michael | |
| dc.contributor.author | Hauser, Karin | |
| dc.date.accessioned | 2023-11-28T14:41:57Z | |
| dc.date.available | 2023-11-28T14:41:57Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Membranes are crucial for the functionality of membrane proteins in several cellular processes. Time-resolved infrared (IR) spectroscopy enables the investigation of interaction-induced dynamics of the protein and the lipid membrane. The photoreceptor and proton pump bacteriorhodopsin (BR) was reconstituted into liposomes, mimicking the native purple membrane. By utilization of deuterated lipid alkyl chains, corresponding vibrational modes are frequency-shifted into a spectrally silent window that allows us to monitor lipid dynamics during the photoreaction of BR. Our home-built quantum cascade laser (QCL)-based IR spectrometer covers all relevant spectral regions to detect both lipid and protein vibrational modes. QCL-probed transients at single wavenumbers are compared with the previously performed step-scan Fourier-transform IR measurements. The absorbance changes of the lipids could be resolved by QCL-measurements with a much better signal-to-noise ratio and with nanosecond time resolution. We found a correlation of the lipid dynamics with the protonation dynamics in the M intermediate. QCL spectroscopy extends the study of the protein’s photocycle toward dynamics of the interacting membrane. | |
| dc.description.version | published | deu |
| dc.identifier.doi | 10.1063/5.0139808 | |
| dc.identifier.ppn | 1879618230 | |
| dc.identifier.uri | https://kops.uni-konstanz.de/handle/123456789/68517 | |
| dc.language.iso | eng | |
| dc.subject.ddc | 540 | |
| dc.title | Mid-IR quantum cascade laser spectroscopy to resolve lipid dynamics during the photocycle of bacteriorhodopsin | eng |
| dc.type | JOURNAL_ARTICLE | |
| dspace.entity.type | Publication | |
| kops.citation.bibtex | @article{Stritt2023MidIR-68517,
year={2023},
doi={10.1063/5.0139808},
title={Mid-IR quantum cascade laser spectroscopy to resolve lipid dynamics during the photocycle of bacteriorhodopsin},
number={15},
volume={158},
issn={0021-9606},
journal={The Journal of Chemical Physics},
author={Stritt, Paul and Jawurek, Michael and Hauser, Karin},
note={Article Number: 154202}
} | |
| kops.citation.iso690 | STRITT, Paul, Michael JAWUREK, Karin HAUSER, 2023. Mid-IR quantum cascade laser spectroscopy to resolve lipid dynamics during the photocycle of bacteriorhodopsin. In: The Journal of Chemical Physics. AIP Publishing. 2023, 158(15), 154202. ISSN 0021-9606. eISSN 1089-7690. Available under: doi: 10.1063/5.0139808 | deu |
| kops.citation.iso690 | STRITT, Paul, Michael JAWUREK, Karin HAUSER, 2023. Mid-IR quantum cascade laser spectroscopy to resolve lipid dynamics during the photocycle of bacteriorhodopsin. In: The Journal of Chemical Physics. AIP Publishing. 2023, 158(15), 154202. ISSN 0021-9606. eISSN 1089-7690. Available under: doi: 10.1063/5.0139808 | eng |
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<dcterms:abstract>Membranes are crucial for the functionality of membrane proteins in several cellular processes. Time-resolved infrared (IR) spectroscopy enables the investigation of interaction-induced dynamics of the protein and the lipid membrane. The photoreceptor and proton pump bacteriorhodopsin (BR) was reconstituted into liposomes, mimicking the native purple membrane. By utilization of deuterated lipid alkyl chains, corresponding vibrational modes are frequency-shifted into a spectrally silent window that allows us to monitor lipid dynamics during the photoreaction of BR. Our home-built quantum cascade laser (QCL)-based IR spectrometer covers all relevant spectral regions to detect both lipid and protein vibrational modes. QCL-probed transients at single wavenumbers are compared with the previously performed step-scan Fourier-transform IR measurements. The absorbance changes of the lipids could be resolved by QCL-measurements with a much better signal-to-noise ratio and with nanosecond time resolution. We found a correlation of the lipid dynamics with the protonation dynamics in the M intermediate. QCL spectroscopy extends the study of the protein’s photocycle toward dynamics of the interacting membrane.</dcterms:abstract>
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| source.publisher | AIP Publishing |
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