Poly-N-acetyllactosamine synthesis in branched N-glycans is controlled by complemental branch specificity of i-extension enzyme and β1,4-galactosyltransferase I

被引:55
作者
Ujita, M
McAuliffe, J
Hindsgaul, O
Sasaki, K
Fukuda, MN
Fukuda, M
机构
[1] Burnham Inst, Ctr Canc Res, Glycobiol Program, La Jolla, CA 92037 USA
[2] Kyowa Hakko Kogyo Co Ltd, Tokyo Res Labs, Machida, Tokyo 194, Japan
关键词
D O I
10.1074/jbc.274.24.16717
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly-N-acetyllactosamine is a unique carbohydrate that can carry various functional oligosaccharides, such as sialyl Lewis X. It has been shown that the amount of poly-N-acetyllactosamine is increased in N-glycans, when they contain Gal beta 1 --> 4GlcNAc beta 1 --> 6(Gal beta 1 --> 4GlcNAc beta 1 --> 2)Man alpha 1 --> branched structure. To determine how this increased synthesis of poly-N-acetyllactosamines takes place, the branched acceptor was incubated with a mixture of i-extension enzyme (iGnT) and beta 1,4-galactosyltransferase I(beta 4Gal-TI), First, N-acetyllactosamine repeats were more readily added to the branched acceptor than the summation of poly-N-acetyllactosamines formed individually on each unbranched acceptor. Surprisingly, poly-N-acetyllactosamine was more efficiently formed on Gal beta 1 --> 4GlcNAc beta 1 --> 2Man alpha --> R side chain than in Gal beta 1 --> 4GlcNAc beta 1 --> 6Man alpha --> R, due to preferential action of iGnT on Gal beta 1 --> 4GlcNAc beta 1 --> 2Man alpha --> R side chain. On the other hand, galactosylation was much more efficient on pl,G-linked GlcNAc than beta 1,a-linked GlcNAc, preferentially forming Gal beta 1 --> 4GlcNAc beta 1 --> 6(GlcNA beta 1 --> 2)Man alpha 1 --> 6Man beta --> R. Starting with this preformed acceptor, N-acetyllactosamine repeats were added almost equally to Gal beta 1 --> 4GlcNAc beta 1 --> 6Man alpha --> R and Gal beta 1 --> 4GlcNA beta 1 --> 2Man alpha --> R side chains. Taken together, these results indicate that the complemental branch specificity of iGnT and beta 4Gal-TI leads to efficient and equal addition of N-acetyllactosamine repeats on both side chains of GlcNAc beta 1 --> 6(GlcNAc beta 1 --> 2)Man alpha 1 --> 6Man beta --> R structure, which is consistent with the structures found in nature. The results also suggest that the addition of Gal beta 1 --> 4GlcNA beta 1 --> 6 side chain on Gal beta 1 --> 4GlcNAc beta 1 --> 2Man --> R side chain converts the acceptor to one that is much more favorable for iGnT and beta 4Gal-TI.
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页码:16717 / 16726
页数:10
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