Literature DB >> 17718555

In situ localization and structural analysis of the malaria pigment hemozoin.

Torsten Frosch1, Sasa Koncarevic, Linda Zedler, Michael Schmitt, Karla Schenzel, Katja Becker, Jürgen Popp.   

Abstract

Raman microspectroscopy was applied for an in situ localization of the malaria pigment hemozoin in Plasmodium falciparum-infected erythrocytes. The Raman spectra (lambdaexc=633 nm) of hemozoin show very intense signals with a very good signal-to-noise ratio. These in situ Raman signals of hemozoin were compared to Raman spectra of extracted hemozoin, of the synthetic analogue beta-hematin, and of hematin and hemin. beta-Hematin was synthesized according to the acid-catalyzed dehydration of hematin and the anhydrous dehydrohalogenation of hemin which lead to good crystals with lengths of about 5-30 microm. The Raman spectra (lambdaexc=1064 nm) of hemozoin and beta-hematin show almost identical behaviors, while some low wavenumber modes might be used to distinguish between the morphology of differently synthesized beta-hematin samples. The intensity pattern of the resonance Raman spectra (lambdaexc=568 nm) of hemozoin and beta-hematin differ significantly from those of hematin and hemin. The most striking difference is an additional band at 1655 cm(-1) which was only observed in the spectra of hemozoin and beta-hematin and cannot be seen in the spectra of hematin and hemin. Raman spectra of the beta-hematin dimer were calculated ab initio (DFT) for the first time and used for an assignment of the experimentally derived Raman bands. The calculated atomic displacements provide valuable insight into the most important molecular vibrations of the hemozoin dimer. With help from these DFT calculations, it was possible to assign the Raman band at 1655 cm(-1) to a mode located at the propionic acid side chain, which links the hemozoin dimers to each other. The Raman band at 1568 cm(-1), which has been shown to be influenced by an attachment of the antimalarial drug chloroquine in an earlier study, could be assigned to a C=C stretching mode spread across one of the porphyrin rings and is therefore expected to be influenced by a pi-pi-stacking to the drug.

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Year:  2007        PMID: 17718555     DOI: 10.1021/jp071788b

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  5 in total

1.  Integration of diffraction phase microscopy and Raman imaging for label-free morpho-molecular assessment of live cells.

Authors:  Rishikesh Pandey; Renjie Zhou; Rosalie Bordett; Ciera Hunter; Kristine Glunde; Ishan Barman; Tulio Valdez; Christine Finck
Journal:  J Biophotonics       Date:  2018-12-13       Impact factor: 3.207

2.  Combined confocal Raman and quantitative phase microscopy system for biomedical diagnosis.

Authors:  Jeon Woong Kang; Niyom Lue; Chae-Ryon Kong; Ishan Barman; Narahara C Dingari; Stephen J Goldfless; Jacquin C Niles; Ramachandra R Dasari; Michael S Feld
Journal:  Biomed Opt Express       Date:  2011-08-01       Impact factor: 3.732

3.  Malaria in cynomolgus monkeys used in toxicity studies in Japan.

Authors:  Etsuko Ohta; Yuko Nagayama; Naoki Koyama; Dai Kakiuchi; Satoru Hosokawa
Journal:  J Toxicol Pathol       Date:  2015-11-20       Impact factor: 1.628

4.  Towards ultrasensitive malaria diagnosis using surface enhanced Raman spectroscopy.

Authors:  Keren Chen; Clement Yuen; Yaw Aniweh; Peter Preiser; Quan Liu
Journal:  Sci Rep       Date:  2016-02-09       Impact factor: 4.379

5.  Malaria pigment crystals as magnetic micro-rotors: key for high-sensitivity diagnosis.

Authors:  A Butykai; A Orbán; V Kocsis; D Szaller; S Bordács; E Tátrai-Szekeres; L F Kiss; A Bóta; B G Vértessy; T Zelles; I Kézsmárki
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

  5 in total

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