TY - JOUR
T1 - Structure of the lipid-linked oligosaccharides that accumulate in class E Thy-1-negative mutant lymphomas
AU - Chapman, Ann
AU - Trowbridge, Ian S.
AU - Hyman, Robert
AU - Kornfeld, Stuart
N1 - Funding Information:
We thank Mrs. Karen Fugimoto for her excellent technical assistance. This investigation was supported by grants from the USPHS.
PY - 1979/7
Y1 - 1979/7
N2 - Studies reported in the preceding paper (Trowbridge and Hyman, 1979) have demonstrated that Thy-1- mutant lymphoma cells of the class E complementation group lack the normal high molecular weight lipid-linked oligosaccharide, but instead accumulate two smaller species termed I and II. This paper reports studies which elucidate the structures of lipid-linked oligosaccharides I and II. By subjecting oligosaccharides radiolabeled with 3H-mannose, 3H-glucose or 3H-glucosamine to methylation, acetolysis, periodate oxidation and exoglycosidase digestion, the structures were shown to be: where R = GlcNac B1,4(3) GlcNAc. A comparison of I and II with lipid-linked oligosaccharides from normal Chinese hamster ovary cells indicates that both I and II are normal biosynthetic intermediates. On the basis of these data we suggest that the defect in the class E mutant cells is the lack of an α1,3 mannosyltransferase involved in the conversion of the Man5GlcNAc2 lipid-linked oligosaccharide to the Man6GlcNAc2 intermediate. It is also impossible that the same enzyme is involved in conversion of the Glc3Man5GlcNAc2 lipid-linked oligosaccharide to Glc3Man6GlcNAc2. The latter reaction, however, has not yet been demonstrated in normal cells.
AB - Studies reported in the preceding paper (Trowbridge and Hyman, 1979) have demonstrated that Thy-1- mutant lymphoma cells of the class E complementation group lack the normal high molecular weight lipid-linked oligosaccharide, but instead accumulate two smaller species termed I and II. This paper reports studies which elucidate the structures of lipid-linked oligosaccharides I and II. By subjecting oligosaccharides radiolabeled with 3H-mannose, 3H-glucose or 3H-glucosamine to methylation, acetolysis, periodate oxidation and exoglycosidase digestion, the structures were shown to be: where R = GlcNac B1,4(3) GlcNAc. A comparison of I and II with lipid-linked oligosaccharides from normal Chinese hamster ovary cells indicates that both I and II are normal biosynthetic intermediates. On the basis of these data we suggest that the defect in the class E mutant cells is the lack of an α1,3 mannosyltransferase involved in the conversion of the Man5GlcNAc2 lipid-linked oligosaccharide to the Man6GlcNAc2 intermediate. It is also impossible that the same enzyme is involved in conversion of the Glc3Man5GlcNAc2 lipid-linked oligosaccharide to Glc3Man6GlcNAc2. The latter reaction, however, has not yet been demonstrated in normal cells.
UR - http://www.scopus.com/inward/record.url?scp=0018581477&partnerID=8YFLogxK
U2 - 10.1016/0092-8674(79)90259-9
DO - 10.1016/0092-8674(79)90259-9
M3 - Article
C2 - 476829
AN - SCOPUS:0018581477
SN - 0092-8674
VL - 17
SP - 509
EP - 515
JO - Cell
JF - Cell
IS - 3
ER -