TY - JOUR
T1 - Structural elucidation of n-linked sugar chains of storage glycoproteins in mature pea (pisum sativum) seeds by ion-spray tandem mass spectrometry (IS-MS/MS)
AU - Kimura, Yoshinobu
AU - Ohno, Akira
AU - Takagi, Shigeaki
N1 - Funding Information:
Materials. Pisum sativum L. cv. Midoriusui was purchased from Takayama Seed Co. (Kyoto, Japan). A Cosmosil 5CI8-AR column (0.60 x 25 cm) was purchased from Nacalai Tesque, Inc., and an Asahipak NH2P-50 column (0.46 x 25 cm) from Showa Denko Co. a-Mannosidase t This work was supported in part by grants from the Ministry of Education, Science, and Culture of Japan (No. 07660442, 1995-1996), from the Ryobi Tei-en Foundation for Biological Research (\995). • To whom all correspondence should be addressed.
PY - 1996/1
Y1 - 1996/1
N2 - The structures of N-linked sugar chains of the storage glycoproteins in mature pea seeds have been estimated. Nine pyridylaminated (PA-) N-linked sugar chains were derived and purified from the hydrazinolysate of the storage glycoproteins by reversed-phase HPLC and size-fractionation HPLC. The structures of the PA-sugar chains purified were first identified by two-dimensional PA-sugar chain mapping, considering the data of sugar composition analysis or sequential exoglycosidase digestions. The deduced structures were further analyzed by IS-MS/MS analysis. Every relevant fragment ion derived from all PA-sugar chains could be assigned on the basis of deduced structures. The estimated nine structures fell into two categories; the first was a typical oligomannose type (Man8-3GlcNAc2; 77.7%) which can be hydrolyzed by endo-β-N-acetylglucosaminidase PS [Y. Kimura et al., Biosci. Biotech. Biochem., 60, 228–232 (1996)], the second was a xylose-containing type (Man4-3Xyl1GlcNAc2, Man3Fuc1Xyl1GlcNAc2; 22.3%). Among these structures, Man8GlcNAc2 (19.7%), Man6GlcNAc2 (24.7%), and Man3Fuc1Xyl1GlcNAc2 (18.8%) were the dominant structures.
AB - The structures of N-linked sugar chains of the storage glycoproteins in mature pea seeds have been estimated. Nine pyridylaminated (PA-) N-linked sugar chains were derived and purified from the hydrazinolysate of the storage glycoproteins by reversed-phase HPLC and size-fractionation HPLC. The structures of the PA-sugar chains purified were first identified by two-dimensional PA-sugar chain mapping, considering the data of sugar composition analysis or sequential exoglycosidase digestions. The deduced structures were further analyzed by IS-MS/MS analysis. Every relevant fragment ion derived from all PA-sugar chains could be assigned on the basis of deduced structures. The estimated nine structures fell into two categories; the first was a typical oligomannose type (Man8-3GlcNAc2; 77.7%) which can be hydrolyzed by endo-β-N-acetylglucosaminidase PS [Y. Kimura et al., Biosci. Biotech. Biochem., 60, 228–232 (1996)], the second was a xylose-containing type (Man4-3Xyl1GlcNAc2, Man3Fuc1Xyl1GlcNAc2; 22.3%). Among these structures, Man8GlcNAc2 (19.7%), Man6GlcNAc2 (24.7%), and Man3Fuc1Xyl1GlcNAc2 (18.8%) were the dominant structures.
KW - Endo-β-N-acetylglucosaminidase-PS
KW - IS-MS/MS
KW - N-linked sugar chain
KW - Pisum sativum
KW - Plant glycoprotein
UR - http://www.scopus.com/inward/record.url?scp=0030455768&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0030455768&partnerID=8YFLogxK
U2 - 10.1271/bbb.60.1841
DO - 10.1271/bbb.60.1841
M3 - Article
C2 - 8987862
AN - SCOPUS:0030455768
SN - 0916-8451
VL - 60
SP - 1841
EP - 1850
JO - Bioscience, Biotechnology and Biochemistry
JF - Bioscience, Biotechnology and Biochemistry
IS - 11
ER -