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人表皮生长因子。高分辨率溶液结构及其与人转化生长因子α的比较。

Human epidermal growth factor. High resolution solution structure and comparison with human transforming growth factor alpha.

作者信息

Hommel U, Harvey T S, Driscoll P C, Campbell I D

机构信息

Department of Biochemistry, Oxford, U.K.

出版信息

J Mol Biol. 1992 Sep 5;227(1):271-82. doi: 10.1016/0022-2836(92)90697-i.

Abstract

The solution structure of the 53 amino acid peptide hormone, human epidermal growth factor (hEGF), has been determined to high resolution from nuclear magnetic resonance (n.m.r.) data. A large number of internuclear distance and dihedral restraints was obtained, including data from uniformly 15N-labelled hEGF. Dynamical simulated annealing methods using the program XPLOR were used for structure calculation. An improved protocol was developed combining efficient conformational searching at a reduced computational cost. The general fold of the calculated structures compared well with that of a derivative of the carboxy-terminally truncated hEGF determined previously. A group of 44 structures were calculated with no violations greater than 0.3 A and 3 degrees for distance and dihedral restraints, respectively. The average pairwise root mean square (r.m.s.) deviation of all backbone atoms for these structures was 2.25 A for all 53 residues, 0.92 A for the bulk of the protein, and 0.23 A for the functionally important carboxy-terminal domain. Two new helical segments containing highly conserved amino acids have been identified; one between cysteines 6 and 14 and a second at the end of the carboxy-terminal domain. New insight into the molecular architecture of the site of putative receptor binding was provided by comparing the structure of hEGF with its biologically equipotent analogue, human transforming growth factor alpha. This comparison revealed a close structural relationship between the two growth factors and provides an improved understanding of the structure/function relationships in EGF.

摘要

已通过核磁共振(n.m.r.)数据将53个氨基酸的肽激素——人表皮生长因子(hEGF)的溶液结构解析到高分辨率。获得了大量核间距离和二面角约束,包括来自均匀15N标记的hEGF的数据。使用XPLOR程序的动态模拟退火方法进行结构计算。开发了一种改进的方案,以降低计算成本并高效进行构象搜索。计算得到的结构的总体折叠与先前确定的羧基末端截短的hEGF衍生物的折叠情况良好匹配。计算了一组44个结构,其距离和二面角约束的违规分别不大于0.3 Å和3°。这些结构中所有主链原子的平均成对均方根(r.m.s.)偏差对于所有53个残基为2.25 Å,对于蛋白质主体为0.92 Å,对于功能重要的羧基末端结构域为0.23 Å。已鉴定出两个包含高度保守氨基酸的新螺旋片段;一个在半胱氨酸6和14之间,另一个在羧基末端结构域的末端。通过比较hEGF与其生物学等效类似物人转化生长因子α的结构,对假定受体结合位点的分子结构有了新的认识。这种比较揭示了两种生长因子之间密切的结构关系,并增进了对EGF中结构/功能关系的理解。

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