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GalNAcβ1,3-linked paragloboside carries the epitope of a sperm maturation-related glycoprotein that is recognized by the monoclonal antibody MC121
► mAb MC121 reacted with a desialylated 43 kDa glycoprotein of mouse spermatozoa. ► Sperm increased expression of the antigenic determinant during epididymal transit. ► The reactivities were diminished after β- N-acetylhexosaminidase treatment. ► MC121 reacted with IV 3GalNAcβ- nLc 4Cer of human red...
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Published in: | Biochemical and biophysical research communications 2011-03, Vol.406 (3), p.326-331 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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Online Access: | Get full text |
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Summary: | ► mAb MC121 reacted with a desialylated 43
kDa glycoprotein of mouse spermatozoa. ► Sperm increased expression of the antigenic determinant during epididymal transit. ► The reactivities were diminished after β-
N-acetylhexosaminidase treatment. ► MC121 reacted with IV
3GalNAcβ-
nLc
4Cer of human red blood cells. ► The minimum epitope was thought to be GalNAcβ1-3Galβ1.
The functional maturation of spermatozoa during epididymal transit in mammals accompanies the changes in their plasma membrane due to the binding or removal of proteins or interactions with the proteases, glycosidases and glycosyltransferases present in the epididymis. In order to study the surface changes in spermatozoa during their maturation in the epididymis, we previously established several monoclonal antibodies against the 54
kDa sialoglycoprotein of mouse cauda epididymal spermatozoa, which gradually increased the expression of antigenic determinants during epididymal transit. One of these monoclonal antibodies, MC121, reacted with mouse sperm glycoproteins on a polyvinylidene fluoride membrane after desialylation of the glycoproteins, and the treatment of the desialylated sperm glycoproteins with β-
N-acetylhexosaminidase greatly decreased the expression of the antigenic determinants. In addition to reacting with mouse cauda epididymal spermatozoa, MC121 reacted with human red blood cells (hRBCs). MC121 induced agglutination of sialidase-treated hRBCs and stained hRBCs fixed with formalin vapor much more heavily than it stained hRBCs fixed with methanol. The thin layer chromatography (TLC) immunostaining of the sialidase-treated lipids of hRBCs with MC121 suggested that the epitope-bearing molecule is a glycosphingolipids (GSL), and that MC121 reacts with a pentaose-GSL. Analysis of sialidase-treated GSLs by TLC-Blot-Matrix Assisted Laser Desorption Ionization Time-of-Flight mass spectrometry (MALDI TOF MS) revealed that the GSL bound by MC121 was [HexNAc][HexNAc
+
Hex][Hex][Hex]-Cer. The lipid band stained with mAb TH2, which is specific for a GSL, GalNAcβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ1-ceramide. These results indicated that the epitope to which MC121 binds is present in a neolacto-series GSL, IV
3GalNAcβ-nLc
4Cer
2
The nomenclature for glycosphingolipids follows the recommendations
[26] of the IUPAC-IUB, and the ganglioside nomenclature of Svennerholm
[27] was used.
2
sequence. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/j.bbrc.2011.02.019 |