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与天冬酰胺连接型碳水化合物的核心三甘露糖苷复合的大花蝶豆凝集素的晶体结构。

Crystal structure of the lectin from Dioclea grandiflora complexed with core trimannoside of asparagine-linked carbohydrates.

作者信息

Rozwarski D A, Swami B M, Brewer C F, Sacchettini J C

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

J Biol Chem. 1998 Dec 4;273(49):32818-25. doi: 10.1074/jbc.273.49.32818.

Abstract

The seed lectin from Dioclea grandiflora (DGL) has recently been shown to possess high affinity for 3, 6-di-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranose, the core trimannoside of asparagine-linked carbohydrates, but lower affinity for biantennary complex carbohydrates. In the previous paper, the thermodynamics of DGL binding to deoxy analogs of the core trimannoside and to a biantennary complex carbohydrate were determined by isothermal titration microcalorimetry. The data suggest that DGL recognizes specific hydroxyl groups of the trimannoside similar to that of the jack bean lectin concanavalin A (ConA) (Gupta, D. Dam, T. K., Oscarson, S., and Brewer, C. F. (1997) J. Biol. Chem. 272, 6388-6392). However, the thermodynamics of DGL binding to certain deoxy analogs and to the complex carbohydrate are different from that of ConA. In the present paper, the x-ray crystal structure of DGL complexed to the core trimannoside was determined to a resolution of 2.6 A. The overall structure of the DGL complex is similar to the structure of the ConA-trimannoside complex (Naismith, J. H., and Field, R. A. (1996) J. Biol. Chem. 271, 972-976). The location and conformation of the bound trimannoside as well as its hydrogen-bonding interactions in both complexes are nearly identical. However, differences exist in the location of two loops outside of the respective binding sites containing residues 114-125 and 222-227. The latter residues affect the location of a network of hydrogen-bonded water molecules that interact with the trisaccharide. Differences in the arrangement of ordered water molecules in the binding site and/or protein conformational differences outside of the binding site may account for the differences in the thermodynamics of binding of the two lectins to deoxy analogs of the trimannoside. Molecular modeling studies suggest how DGL discriminates against binding the biantennary complex carbohydrate relative to ConA.

摘要

大花蝶豆(Dioclea grandiflora)的种子凝集素(DGL)最近被证明对3,6-二-O-(α-D-甘露吡喃糖基)-α-D-甘露吡喃糖(天冬酰胺连接碳水化合物的核心三甘露糖苷)具有高亲和力,但对双触角复合碳水化合物的亲和力较低。在之前的论文中,通过等温滴定量热法测定了DGL与核心三甘露糖苷的脱氧类似物以及双触角复合碳水化合物结合的热力学。数据表明,DGL识别三甘露糖苷的特定羟基,这与刀豆凝集素伴刀豆球蛋白A(ConA)类似(古普塔,D. 达姆,T. K.,奥斯卡森,S.,以及布鲁尔,C. F.(1997年)《生物化学杂志》272,6388 - 6392)。然而,DGL与某些脱氧类似物以及复合碳水化合物结合的热力学与ConA不同。在本文中,测定了与核心三甘露糖苷复合的DGL的X射线晶体结构,分辨率为2.6埃。DGL复合物的整体结构与ConA - 三甘露糖苷复合物的结构相似(奈史密斯,J. H.,以及菲尔德,R. A.(1996年)《生物化学杂志》271,972 - 976)。两种复合物中结合的三甘露糖苷的位置和构象以及其氢键相互作用几乎相同。然而。在各自结合位点之外包含残基114 - 125和222 - 227的两个环的位置存在差异。后一组残基影响与三糖相互作用的氢键水分子网络的位置。结合位点中有序水分子排列的差异和/或结合位点之外的蛋白质构象差异可能解释了两种凝集素与三甘露糖苷脱氧类似物结合热力学的差异。分子模拟研究表明了DGL相对于ConA如何区分不结合双触角复合碳水化合物。

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