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刺桐种子中半乳糖特异性异凝集素的两个亚基,A亚基和B亚基的化学结构。

Chemical structures of two subunits, A-subunit and B-subunit, of galactose-specific isolectins from Erythrina variegata seeds.

作者信息

Yamaguchi O, Kimura M, Araki M, Yamasaki N, Kimura Y, Nakajima S, Takagi S

机构信息

Laboratory of Biochemistry, Faculty of Agriculture, Kyushu University, Fukuoka.

出版信息

J Biochem. 1993 Oct;114(4):560-6. doi: 10.1093/oxfordjournals.jbchem.a124216.

Abstract

We previously isolated galactose-specific isolectins, EVLI, EVLII, and EVLIII, from the Erythrina variegata seeds [J. Chromatogr. 597, 207-211 (1992)]. The amino acid sequences of the two subunits, A- and B-subunits, of which the isolectins are composed, were determined. A comparison of the amino acid sequences of tryptic peptides from the two subunits revealed seven amino acid substitutions. Among them, Asn46, to which the oligosaccharide chain is linked in the A-subunit, is replaced by Asp46 in the B-subunit, causing the B-subunit to lack one glycosylation site. The N-linked oligosaccharides of these subunits were also analyzed. The N-linked oligosaccharides were first liberated by hydrazinolysis. After N-acetylation, the reducing ends of the oligosaccharides were coupled with 2-aminopyridine, and then the pyridylamino (PA-) derivatives were purified by gel filtration and HPLC on an ODS-silica column. One major sugar chain, accounting for more than 98% of the total, was purified from both species. The structure of this major sugar chain was established to be Man alpha 6(Man alpha 3)(Xyl beta 2)Man beta 4GlcNAc beta 4(Fuc alpha 3)GlcNAc. This finding that there is no structural difference of the sugar chains linked to the two subunits of E. variegata lectins, together with the results of amino acid sequence comparisons, indicates that the difference in molecular mass of these two subunits results almost wholly from the difference in the number of oligosaccharides linked to them.

摘要

我们之前从刺桐种子中分离出了半乳糖特异性异凝集素EVLI、EVLII和EVLIII [《色谱杂志》597, 207 - 211 (1992)]。测定了构成这些异凝集素的两个亚基(A亚基和B亚基)的氨基酸序列。对这两个亚基的胰蛋白酶肽段氨基酸序列进行比较,发现有七个氨基酸替换。其中,A亚基中连接寡糖链的Asn46在B亚基中被Asp46取代,导致B亚基缺少一个糖基化位点。还对这些亚基的N - 连接寡糖进行了分析。N - 连接寡糖首先通过肼解释放出来。N - 乙酰化后,寡糖的还原端与2 - 氨基吡啶偶联,然后通过凝胶过滤和在ODS - 硅胶柱上的高效液相色谱法纯化吡啶氨基(PA -)衍生物。从这两个种类中都纯化出了一种占总量98%以上的主要糖链。该主要糖链的结构确定为Manα6(Manα3)(Xylβ2)Manβ4GlcNAcβ4(Fucα3)GlcNAc。刺桐凝集素两个亚基连接糖链不存在结构差异这一发现,连同氨基酸序列比较结果表明,这两个亚基分子量的差异几乎完全源于与其连接的寡糖数量的差异。

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