期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 23, 期 31, 页码 16635-16645出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cp02574k
关键词
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资金
- Ministry of Education [CZ.02.1.01/0.0/0.0/16_019/0000729]
- Science Foundation of the Czech Republic [20-10144S]
Researchers used VOA technology to study alpha-synuclein, successfully revealing the spectral features of different conformations through computational simulations and experimental analysis. They discovered previously unreported ROA marker bands of secondary structure, and successfully simulated fibril VCD spectra.
alpha-Synuclein is a neuronal protein which adopts multiple conformations. These can be conveniently studied by the spectroscopy of vibrational optical activity (VOA). However, the interpretation of VOA spectra based on quantum-chemical simulations is difficult. To overcome the hampering of the computations by the protein size, we used the Cartesian tensor transfer technique to investigate links between the spectral shapes and protein structure. Vibrational circular dichroism (VCD) and Raman optical activity (ROA) spectra of alpha-synuclein in disordered, alpha-helical and beta-sheet (fibril) forms were measured and analyzed on the basis of molecular dynamics and density functional theory computations. For the disordered and alpha-helical conformers, a high fidelity of the simulated spectra with a reasonable computational cost was achieved. Most experimental spectral features could be assigned to the structure. So far unreported ROA marker bands of the secondary structure were found for the lower-frequency and CH stretching vibrations. Fibril VCD spectra were simulated with a rigid periodic model of the geometry and the results are consistent with previous studies based on cryogenic electron microscopy. The fibrils also give a specific ROA signal, but unlike VCD it is currently not fully explicable by the simulations. In connection with the computational modeling the VOA spectroscopy thus appears as an extremely useful tool for monitoring alpha-synuclein and other proteins in solutions.
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