TY - JOUR
T1 - Biochemical characterization of inner sugar chains of acrosome reaction-inducing substance in jelly coat of starfish eggs
AU - Gunaratne, H. M.M.Jayantha
AU - Yamagaki, Tohru
AU - Matsumoto, Midori
AU - Hoshi, Motonori
N1 - Funding Information:
We express our gratitude to Prof. Ann Dell of the Imperial College of Science, Technology and Medicine, U.K., for critical commentary on this manuscript and Prof. M. Ueda of Keio University, Japan, and Prof. Tachibana of University of Tokyo for making arrangements for the NMR analysis and mass analysis. We also thank Dr. W.M.S. Wimalasiri of University of Peradeniya, Sri Lanka; Drs. H. Nishida, T. Baginzki, and M. Kawamura of Tokyo Institute of Technology; and Prof. Y. Ohashi of University of Electro-communications, Japan, for helpful advice and discussions. We thank the directors and the staff of Otsuchi, Misaki, Ushimado Marine Biological Centers and Stations in Japan and Marine and Coastal Research, Tasmania, Australia, for help in collecting starfish. H.M.M.J.G. is supported by the Ministry of Education, Science and Culture, Japan, and is currently on leave from the Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
PY - 2003/8/1
Y1 - 2003/8/1
N2 - The inception of the acrosome reaction (AR) in the starfish Asterias amurensis is perceived to be strongly associated with sulfated polysaccharide chains derived from an extremely large proteoglycan-like molecule called AR-inducing substance (ARIS), in which one of the sugar fragments, named fragment 1 (Fr. 1), was composed of the repeating units of [→4]-β-D-Xylp-(1→3)-α-D-Galp-(1→3 -α-L-Fucp-4(SO3-)-(1→3)-α-L -Fucp-4(SO3-)-(1→4)-α-L-Fucp-(1→ n. In the current study, this sugar chain is inferred to link to the peptide part by O-glycosidic linkage through a sugar chain with different structural features from Fr. 1. This inner sugar portion of ARIS was isolated as Fr. 2 from the sonicated products of pronase digest of ARIS. Fr. 2, which retains AR-inducing activity to an admirable extent and has an apparent molecular size of 400 kDa, is composed of Gal, Xyl, Fuc, GalNAc, and GlcNAc in a molar ratio of 5:1:5:4:2 with O-sulfate substitutions at Gal-4, Gal-2, Gal-2,3 and Gal-2,4 (disulfated), Fuc-4, and GlcNAc-6. The study of Fr. 2 revealed that the major portion of the inner sugar chain of ARIS is composed of the heptasaccharide units of →3)-Galp-(1→3)-Fucp-(1→3)-Galp-(1→4 -GalNAcp-(1→4)-GlcNAcp-6(SO3-) -(1→6 -Galp-4(SO3-)-(1→4)-GalNAcp-(1→. This new structure of inner sugar chains of ARIS is elucidated by using electrospray ionization MS along with tandem mass analysis, sugar composition analysis, and methylation analysis of the sugar fragments obtained by acid-catalyzed resin-based partial hydrolysis of Fr. 2. Furthermore, this study corroborates that the sulfate groups are solely liable to the anionic character of ARIS, which ought to be present in the sugar chains of ARIS for its biological activity.
AB - The inception of the acrosome reaction (AR) in the starfish Asterias amurensis is perceived to be strongly associated with sulfated polysaccharide chains derived from an extremely large proteoglycan-like molecule called AR-inducing substance (ARIS), in which one of the sugar fragments, named fragment 1 (Fr. 1), was composed of the repeating units of [→4]-β-D-Xylp-(1→3)-α-D-Galp-(1→3 -α-L-Fucp-4(SO3-)-(1→3)-α-L -Fucp-4(SO3-)-(1→4)-α-L-Fucp-(1→ n. In the current study, this sugar chain is inferred to link to the peptide part by O-glycosidic linkage through a sugar chain with different structural features from Fr. 1. This inner sugar portion of ARIS was isolated as Fr. 2 from the sonicated products of pronase digest of ARIS. Fr. 2, which retains AR-inducing activity to an admirable extent and has an apparent molecular size of 400 kDa, is composed of Gal, Xyl, Fuc, GalNAc, and GlcNAc in a molar ratio of 5:1:5:4:2 with O-sulfate substitutions at Gal-4, Gal-2, Gal-2,3 and Gal-2,4 (disulfated), Fuc-4, and GlcNAc-6. The study of Fr. 2 revealed that the major portion of the inner sugar chain of ARIS is composed of the heptasaccharide units of →3)-Galp-(1→3)-Fucp-(1→3)-Galp-(1→4 -GalNAcp-(1→4)-GlcNAcp-6(SO3-) -(1→6 -Galp-4(SO3-)-(1→4)-GalNAcp-(1→. This new structure of inner sugar chains of ARIS is elucidated by using electrospray ionization MS along with tandem mass analysis, sugar composition analysis, and methylation analysis of the sugar fragments obtained by acid-catalyzed resin-based partial hydrolysis of Fr. 2. Furthermore, this study corroborates that the sulfate groups are solely liable to the anionic character of ARIS, which ought to be present in the sugar chains of ARIS for its biological activity.
KW - ARIS
KW - Acrosome reaction
KW - CID MS-MS
KW - Egg jelly coat
KW - Sulfated glycans
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U2 - 10.1093/glycob/cwg070
DO - 10.1093/glycob/cwg070
M3 - Article
C2 - 12702668
AN - SCOPUS:0042195995
SN - 0959-6658
VL - 13
SP - 567
EP - 580
JO - Glycobiology
JF - Glycobiology
IS - 8
ER -