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Scanning transmission X-ray microscopic analysis of purified melanosomes of the mouse iris
Authors:Anderson Michael G  Haraszti Tamás  Petersen Greg E  Wirick Sue  Jacobsen Chris  John Simon W M  Grunze Michael
Institution:

aDepartment of Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, United States

bInstitute for Molecular Biophysics, University of Maine, Orono, ME 04469, United States

cInstitute of Physical Chemistry, University of Heidelberg, Heidelberg, Germany

dNational Synchrotron Light Source, Brookhaven National Laboratory, Upton, NY 11973, United States

eDepartment of Physics, SUNY at Stony Brook, Stony Brook, NY 11794, United States

fThe Howard Hughes Medical Institute and The Jackson Laboratory, Bar Harbor, ME 04609, United States

Abstract:Melanosomes are specialized intracellular membrane bound organelles that produce and store melanin pigment. The composition of melanin and distribution of melanosomes determine the color of many mammalian tissues, including the hair, skin, and iris. However, the presence of melanosomes within a tissue carries potentially detrimental risks related to the cytotoxic indole–quinone intermediates produced during melanin synthesis. In order to study melanosomal molecules, including melanin and melanin-related intermediates, we have refined methods allowing spectromicroscopic analysis of purified melanosomes using scanning transmission X-ray microscopy. Here, we present for the first time absorption data for melanosomes at the carbon absorption edge ranging from 284 to 290 eV. High-resolution images of melanosomes at discrete energies demonstrate that fully melanized mature melanosomes are internally non-homogeneous, suggesting the presence of an organized internal sub-structure. Spectra of purified melanosomes are complex, partially described by a predominating absorption band at 288.4 eV with additional contributions from several minor bands. Differences in these spectra were detectable between samples from two strains of inbred mice known to harbor genetically determined melanosomal differences, DBA/2J and C57BL/6J, and are likely to represent signatures arising from biologically relevant and tractable phenomena.
Keywords:Synchrotron radiation  NEXAFS  Organelle structure–function  Melanin  Mammalian genetics
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