Molecular Interactions Identified by Two-Dimensional Analysis-Detailed Insight into the Molecular Interactions of the Antimalarial Artesunate with the Target Structure β-Hematin by Means of 2D Raman Correlation Spectroscopy

被引:7
|
作者
Domes, Robert [1 ]
Frosch, Torsten [1 ,2 ]
机构
[1] Leibniz Inst Photon Technol, D-07745 Jena, Germany
[2] Tech Univ Darmstadt, Biophoton & Biomed Engn Grp, D-64283 Darmstadt, Germany
关键词
DENSITY-FUNCTIONAL THEORY; STERICALLY INDUCED DISTORTIONS; LIANA TRIPHYOPHYLLUM-PELTATUM; ALKALOID DIONCOPHYLLINE-A; EFFECTIVE CORE POTENTIALS; RESONANCE RAMAN; PLASMODIUM-FALCIPARUM; MALARIA PIGMENT; BETA-HEMATIN; QINGHAOSU ARTEMISININ;
D O I
10.1021/acs.analchem.3c01415
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A thorough understandingof the interaction of endoperoxide antimalarial agents with theirbiological target structures is of utmost importance for the tailoreddesign of future efficient antimalarials. Detailed insights into molecularinteractions between artesunate and & beta;-hematin were derived witha combination of resonance Raman spectroscopy, two-dimensional correlationanalysis, and density functional theory calculations. Resonance Ramanspectroscopy with three distinct laser wavelengths enabled the specificexcitation of different chromophore parts of & beta;-hematin. Theresonance Raman spectra of the artesunate-& beta;-hematin complexeswere thoroughly analyzed with the help of high-resolution and highlysensitive two-dimensional correlation spectroscopy. Spectral changesin the peak properties were found with increasing artesunate concentration.Changes in the low-frequency, morphology-sensitive Raman bands indicateda loss in crystallinity of the drug-target complexes. Differencesin the high-wavenumber region were assigned to increased distortionsof the planarity of the structure of the target molecule due to theappearance of various coexisting alkylation species. Evidence forthe appearance of high-valent ferryl-oxo species could be observedwith the help of differences in the peak properties of oxidation-statesensitive Raman modes. To support those findings, the relaxed ground-statestructures of ten possible covalent mono- and di-meso(C-m)-alkylated hematin-dihydroartemisinyl complexes werecalculated using density functional theory. A very good agreementwith the experimental peak properties was achieved, and the out-of-planedisplacements along the lowest-frequency normal coordinates were investigatedby normal coordinate structural decomposition analysis. The strongestchanges in all data were observed in vibrations with a high participationof C-m-parts of & beta;-hematin.
引用
收藏
页码:12719 / 12731
页数:13
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