the combination of resonance raman spectroscopy, optical tweezers and microfluidic systems applied to the study of various heme-containing single cells的组合共振拉曼光谱、光学镊子和微流控系统适用于各种heme-containing单个细胞的研究.pdfVIP
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the combination of resonance raman spectroscopy, optical tweezers and microfluidic systems applied to the study of various heme-containing single cells的组合共振拉曼光谱、光学镊子和微流控系统适用于各种heme-containing单个细胞的研究
Spectroscopy 22 (2008) 287–295 287
DOI 10.3233/SPE-2008-0353
IOS Press
The combination of resonance Raman
spectroscopy, optical tweezers and
microfluidic systems applied to the study
of various heme-containing single cells
K. Ramser a,∗, W. Wenseleers b , S. Dewilde c , S. Van Doorslaer b and L. Moens c
a Department of Computer Science and Electrical Engineering, Luleå University of Technology, Luleå,
Sweden
b Department of Physics, University of Antwerp, Antwerp, Belgium
c Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium
Abstract. Several recent studies on the function of neuroglobin (Ngb), a hemoprotein predominantly expressed in the brain,
point toward a neuro-protective role during hypoxic-ischemic injuries. The exact mechanism by which Ngb protects the cell
against H O -induced cell death remains to be elucidated. Hence, new tools need to be developed in order to study the protein
2 2
in vivo or under physiological conditions. In this summary of our work, we demonstrate how resonance Raman spectroscopy,
optical tweezers and microfluidic systems were combined to mimic in vivo conditions in an in vitro milieu. The setup has been
tested on several globin-containing cells: hemoglobin (Hb) within single red blood cells (RBCs), a nerve globin present in the
nerve cord of the annelid Aphrodite aculeata (A. aculeata), and wild-type (wt) human neuroglobin (NGB) overexpressed in
Escherichia coli (E. coli) bacteria. The feasibility of the setup regarding sensitivity and photo-induced effects and the results
regarding the oxygen uptake and release will be discussed and compared for each system. The summary of the results show
that the method is promising and the setup will be developed further to monitor the dependence of the neuronal action potential
on nerve globins.
Keywords: Neuroglobin, hemoglobin, nerve myoglobin,
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