B. Liszka
University of Twente
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Publication
Featured researches published by B. Liszka.
Experimental Eye Research | 2016
G.F.J.M. Vrensen; Cees Otto; Aufried Lenferink; B. Liszka; Gustavo A. Montenegro; Rafael I. Barraquer; Ralph Michael
A combination of Raman spectroscopy, imaging, hierarchical cluster analysis (HCA) and peak ratio analysis was used to analyze protein profiles in the superficial cortex (SC), deep cortex (DC) and nucleus of old human lenses with cortical, nuclear and mixed cataracts. No consistent differences were observed in protein spectra and after cluster analysis between the three locations irrespective of the presence or absence of cortical opacities and/or coloration. A sharp increase (∼15%-∼33%) in protein content from SC to DC, normal for human lenses, was found in 7 lenses. In 4 lenses, characterized by the absence of cortical opacities, the SC has a protein content of ∼35%. A significant increase in the disulfide-to-protein ratio is found only in the SC of the 7 cortical cataracts. No changes were found in sulfhydryl-to-protein ratio. The relative contents of α-helices and β-sheets increase from SC to nucleus. β-Sheets are more common in the SC of lenses with cortical cataract. The absence of significant and consistent changes in protein profiles between nucleus and cortex even in cases of severe coloration is not favoring the prevailing concept that ubiquitous protein oxidation is a key factor for age related nuclear (ARN) cataracts. The observations favor the idea that multilamellar bodies or protein aggregates at very low volume densities are responsible for the rise in Mie light scatter as a main cause of ARN cataracts leaving the short-range-order of the fiber cytoplasm largely intact. The absence of significant changes in the protein spectra of the deep cortical opacities, milky white as a result of the presence of vesicle-like features, indicate they are packed with relatively undisturbed crystallins.
Journal of analytical and bioanalytical techniques | 2016
B. Liszka; Aufrid T.M. Lenferink; Cornelis Otto
The growth of single, self- nucleated calcium carbonate crystals on a polysulfone (PSU) film was investigated with high resolution, time lapse Raman imaging. The Raman images were acquired on the interface of the polymer with the crystal. The growth of crystals could thus be followed in time. PSU is a polymer that is used as a membrane material in water cleaning technology. The intensity of the Raman band at the position of 1086 cm-1, which is due to the symmetric stretching of the C-O bonds in the carbonate group of calcite was used to translate the number of CO3 2- ions in a crystal to the growth in time. The growth rate of single crystals of calcium carbonate on a surface was obtained from successive Raman images. We are presenting for the first time time-lapse Raman images of single crystal growth as a direct method to determine a crystal growth rate on an industrially relevant membrane material, like polysulfone.
Journal of Raman Spectroscopy | 2015
B. Liszka; Aufried Lenferink; Geert-Jan Witkamp; Cees Otto
Journal of Raman Spectroscopy | 2016
Frank Jan Timmermans; B. Liszka; Aufried Lenferink; H.A.G.M. van Wolferen; Cees Otto
Journal of Raman Spectroscopy | 2016
Frank Jan Timmermans; B. Liszka; Aufrid T.M. Lenferink; Hendricus A.G.M. van Wolferen; Cornelis Otto
Archive | 2015
B. Liszka; Hoon Suk Rho; Yoon Sun Yang; Aufrid T.M. Lenferink; Cornelis Otto
Archive | 2014
B. Liszka; Aufrid T.M. Lenferink; Yoon Sun Yang; Hoon Suk Rho; G.J. Witkamp; Leonardus Wendelinus Mathias Marie Terstappen; Cornelis Otto
Archive | 2014
B. Liszka; Aufrid T.M. Lenferink; Yoon Sun Yang; Hoon Suk Rho; G.J. Witkamp; Leonardus Wendelinus Mathias Marie Terstappen; Cornelis Otto
Archive | 2013
B. Liszka; Aufrid T.M. Lenferink; G.J. Witkamp; Leonardus Wendelinus Mathias Marie Terstappen; Cornelis Otto
15th European Conference on the Spectroscopy Biological Molecules, ECSBM 2013 | 2013
B. Liszka; Aufried Lenferink; Yoon Sun Yang; Hoon Suk Rho; G.J. Witkamp; Leon W.M.M. Terstappen; Cornelis Otto