Glycobiology Advance Access published online on May 2, 2006
Glycobiology, doi:10.1093/glycob/cwj122
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1 Division of Molecular Pathology, Aichi Cancer Center Research Institute, Nagoya, Aichi, Japan
* To whom correspondence should be addressed. By combining the partition method for enrichment of sulfatides without any chromatographic procedures and the preparation method of lysosulfatides, we succeeded in analyzing these sulfated glycosphingolipids from biological materials by MALDI-TOF MS, to reduce the complexity of mass fragmentation patterns within a day. We found that SM4s (galactosylsulfatide) was composed of different species. While composition of SM4s specifically depended on source materials, it always contained hydroxy fatty acids of various degrees. In addition to the common sphingoid 4-sphingenine (d18:1), uncommon/unusual sphingoids phytosphingosine (t18:0), 4-eicosasphinganine (d20:0), 4-eicosasphingenine (d20:1), and sphingadienine (d18:2) were easily detected. Finally, in addition to SM4s, sulfatide SM3 (sulfated lactosylceramide) and SM2 (sulfated gangliotriaosylceramide) were clearly detected in renal tubule cells. The major SM4s was composed of ceramides possessing d18:1 with C22 hydroxy fatty acids (C22:0h), C23:0h, and C24:0h, whereas the major SM3/SM2 were composed of ceramides possessing t18:0 with C22 normal fatty acids (C22:0), C23:0, C24:0. Namely, in these two series of sulfatides, either fatty acids or sphingoids were hydroxylated, and chain lengths of these components were exactly the same, consequently resulting in a similar polarity of ceramide moieties in these sulfatide species. These results demonstrated diversities of sulfatide molecular species, not only with respect to sugar moieties but also to ceramide moieties, which are probably important for specific effective functions in particular microenvironments such as lipid membrane microdomains.
Received January 28, 2006
Revised April 24, 2006
Accepted April 25, 2006
Article
Rapid demonstration of diversity of sulfatide molecular species from biological materials by MALDI-TOF MS
Mamoru Kyogashima 1 *,
Keiko Tamiya-Koizumi 1,
Takashi Ehara 2,
Gang Li 3,
Rui Hu 3,
Atsushi Hara 3,
Toshifumi Aoyama 3,
and
Reiji Kannagi 1
2 Department of Histopathology, Shinshu University School of Medicine, Matsumoto, Nagano, Japan
3 Department of Metabolic Regulation, Institute on Aging and Adaptation, Shinshu University Graduate School of Medicine, Matsumoto, Nagano, Japan
Mamoru Kyogashima, E-mail: mkyogashi{at}aichi-cc.jp
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