Leibniz Institute of Photonic Technology, Albert Einstein Strasse 9, D-07745 Jena, Germany.
Biophotonics and Biomedical Engineering Group, Technical University Darmstadt, Merckstraße 25, 64283 Darmstadt, Germany.
Anal Chem. 2023 Aug 29;95(34):12719-12731. doi: 10.1021/acs.analchem.3c01415. Epub 2023 Aug 16.
A thorough understanding of the interaction of endoperoxide antimalarial agents with their biological target structures is of utmost importance for the tailored design of future efficient antimalarials. Detailed insights into molecular interactions between artesunate and β-hematin were derived with a combination of resonance Raman spectroscopy, two-dimensional correlation analysis, and density functional theory calculations. Resonance Raman spectroscopy with three distinct laser wavelengths enabled the specific excitation of different chromophore parts of β-hematin. The resonance Raman spectra of the artesunate-β-hematin complexes were thoroughly analyzed with the help of high-resolution and highly sensitive two-dimensional correlation spectroscopy. Spectral changes in the peak properties were found with increasing artesunate concentration. Changes in the low-frequency, morphology-sensitive Raman bands indicated a loss in crystallinity of the drug-target complexes. Differences in the high-wavenumber region were assigned to increased distortions of the planarity of the structure of the target molecule due to the appearance of various coexisting alkylation species. Evidence for the appearance of high-valent ferryl-oxo species could be observed with the help of differences in the peak properties of oxidation-state sensitive Raman modes. To support those findings, the relaxed ground-state structures of ten possible covalent mono- and di-(C)-alkylated hematin-dihydroartemisinyl complexes were calculated using density functional theory. A very good agreement with the experimental peak properties was achieved, and the out-of-plane displacements along the lowest-frequency normal coordinates were investigated by normal coordinate structural decomposition analysis. The strongest changes in all data were observed in vibrations with a high participation of C-parts of β-hematin.
深入了解内过氧化物抗疟药物与生物靶结构的相互作用对于精心设计未来高效的抗疟药物至关重要。本研究采用共振拉曼光谱、二维相关分析和密度泛函理论计算相结合的方法,深入研究了青蒿素与β-血红素之间的分子相互作用。三种不同激光波长的共振拉曼光谱能够特异性地激发β-血红素的不同发色团部分。在高分辨率和高灵敏度二维相关光谱的帮助下,对青蒿素-β-血红素复合物的共振拉曼光谱进行了彻底分析。随着青蒿素浓度的增加,发现峰性质的光谱变化。低频、形态敏感拉曼带的变化表明药物-靶复合物的结晶度降低。由于各种共存的烷基化物种的出现,结构的平面性增加,高波数区域的差异被分配到结构的增加的变形。可以通过氧化态敏感拉曼模式的峰性质的差异来观察高价铁氧物种的出现的证据。为了支持这些发现,使用密度泛函理论计算了十个可能的共价单和二(C)-烷基化血红素-青蒿素复合物的松弛基态结构。与实验峰性质非常吻合,并通过正则坐标结构分解分析研究了沿最低频率正则坐标的面外位移。在所有数据中观察到的最强变化是在β-血红素的 C 部分参与度高的振动中。