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Fundamental vibrations of the chromophore in the membrane protein bacteriorhodopsin (BR), a protonated Schiff base retinal, have been studied for decades, both by resonance Raman and by infrared (IR) difference spectroscopy. Such studies started comparing vibrational changes between the initial BR state (all- retinal) and the K intermediate (13- retinal), being later extended to the rest of intermediates. They contributed to our understanding of the proton-pumping mechanism of BR by exploiting the sensitivity of fundamental vibrational transitions of the retinal to its conformation. Here, we report on new bands in the 2,500 to 1,800 cm region of the K-BR difference FT-IR spectrum. We show that the bands between 2,500 and 2,300 cm originate from overtone and combination transitions from C-C stretches of the retinal. We assigned bands below 2,300 cm to the combination of retinal C-C stretches with methyl rocks and with hydrogen-out-of-plane vibrations. Remarkably, experimental C-C overtone bands appeared at roughly twice the wavenumber of their fundamentals, with anharmonic mechanical constants ≤3.5 cm, and in some cases of ∼1 cm. Comparison of combination and fundamental bands indicates that most of the mechanical coupling constants are also very small. Despite the mechanical quasi-harmonicity of the C-C stretches, the area of their overtone bands was only ∼50 to ∼100 times smaller than of their fundamental bands. We concluded that electrical anharmonicity, the second mechanism giving intensity to overtone bands, must be particularly high for the retinal C-C stretches. We corroborated the assignments of negative bands in the K-BR difference FT-IR spectrum by ab initio anharmonic vibrational calculations of all-trans retinal in BR using a quantum-mechanics/molecular mechanics approach, reproducing reasonably well the small experimental anharmonic and coupling mechanical constants. Yet, and in spite accounting for both mechanical and electrical anharmonicities, the intensity of overtone C-C transitions was underestimated by a factor of 4-20, indicating room for improvement in state-of-the-art anharmonic vibrational calculations. The relatively intense overtone and combination bands of the retinal might open the possibility to detect retinal conformational changes too subtle to significantly affect fundamental transitions but leaving a footprint in overtone and combination transitions.
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http://dx.doi.org/10.3389/fmolb.2021.749261 | DOI Listing |
Spectrochim Acta A Mol Biomol Spectrosc
September 2025
Department of Chemistry, University of Copenhagen, Universitetsparken 5, Copenhagen-Ø, DK-2100, Denmark. Electronic address:
Absorption spectra of neopentyl alcohol and pinacolyl alcohol are recorded in the gas phase at room temperature and equilibrium conditions. A combination of conventional Fourier transform spectroscopy and cavity ringdown spectroscopy is used to cover the spectral OH-stretching regions, Δv=1-5. The conformer distributions of the alcohols are determined from the recorded spectra combined with transition intensities calculated with a reduced dimensional local mode model.
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Institute of Physical Chemistry, Clausthal University of Technology, Arnold-Sommerfeld-Str. 4, D-38678 Clausthal-Zellerfeld, Germany.
A fast electrochemical quartz crystal microbalance with dissipation monitoring (EQCM-D) was used to study the formation of hydrogen bubbles at a cathode during water splitting. Different metal surfaces behaved similarly. The kinetics revealed two time scales.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
State Key Laboratory of Porous Materials for Separation and Conversion, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials; Department of Chemistry, Fudan University, Shanghai 200433, China.
The new cyanomethanesulfinyl radical •OSCHCN has been generated in the gas phase by high-vacuum flash pyrolysis (HVFP) of 2-(allylsulfinyl)acetonitrile at ca. 650 K and subsequently isolated in a solid Ar matrix at 10 K for characterization with matrix-isolation infrared (IR) spectroscopy. Upon photoexcitation at 430 nm, •OSCHCN undergoes an unexpected [1,3]-sigmatropic rearrangement to yield the novel keteniminyl-substituted sulfinyl radical CHCNSO• in the matrix, and the reverse isomerization occurs under further irradiation at 532 nm.
View Article and Find Full Text PDFJHEP Rep
August 2025
Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Metabolic dysfunction-associated steatotic liver disease (MASLD) affects more than a quarter of the adult population worldwide. MASLD can progress to metabolic dysfunction-associated steatohepatitis (MASH), which is associated with increased risk of progression to liver fibrosis, cirrhosis and hepatocellular carcinoma, as well as cardiovascular complications. The pathogenesis of MASLD is complex and initiated by altered metabolic signalling circuits between the adipose tissue, muscle, gut and liver.
View Article and Find Full Text PDFJ Phys Chem A
July 2025
Department of Chemistry and Biochemistry, University of Mississippi, University, Mississippi 38677-1848, United States.
Recently developed, reparameterized PM6 methods can reproduce experimental polycyclic aromatic hydrocarbon (PAH) IR spectra with nearly the same accuracy as state-of-the-art quantum chemical methods but for notably less computational cost. The use of the () semiempirical method (as opposed to () for density functional theory or () for the most accurate coupled cluster theory) allows for full, explicit, quartic force field (QFF), anharmonic computations on PAHs. The anharmonicity also predicts the combination band and overtone frequencies in addition to the fundamentals.
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