...
首页> 外文期刊>Journal of Molecular Biology >ROLE OF BETA-TURN RESIDUES IN BETA-HAIRPIN FORMATION AND STABILITY IN DESIGNED PEPTIDES
【24h】

ROLE OF BETA-TURN RESIDUES IN BETA-HAIRPIN FORMATION AND STABILITY IN DESIGNED PEPTIDES

机译:β-转残基在β-发夹形成中的作用和设计肽的稳定性

获取原文
获取原文并翻译 | 示例

摘要

The sequence RGITVNGKTYGR has been reported as part of a de no-do design peptide system. This peptide folds as a beta-hairpin structure with three residues per strand and two residue turns. Asn6 side-chain, the residue in position L1 of the beta-turn, appeared to be solvent exposed, interacting only with in the turn but not with the rest of the peptide. We have chosen this position as a good candidate to design mutations, based on the protein database statistical abundances, that should mainly affect the turn stability and possibly the pairing: between strands. We have found that all NMR parameters, in particular the conformational shift analysis of (CH)-H-alpha and the coupling constants, (3)J(HN alpha), correlate very well and show similar conformational features in all the turn mutant peptides. The population estimates are in reasonable agreement among the different methods used, It appears that the peptide with Asn in position L1 is the most structured peptide, followed by the one with Asp6. The next structured peptide is the one with Gly6. The least populated peptides were those with Ala6 and Ser6. We have found a strong correlation between the hairpin population, as determined from the conformational shift of (CH)-H-alpha and the occurrence of the different residues at position L1 of beta-hairpins with type I' beta-turn, in the protein in database. Our analysis demonstrates that this peptide system is sensitive enough to register small energy changes in the hairpin structure; therefore, it constitutes an appropriate model to quantify energy contributions, once the appropriate sheet/coil transition algorithm is developed. Comparison with the other studies indicate that the design of a specific hairpin structure must involve a sequence at the rum region favouring the desired turn type, and a sequence at the strands that avoids alternative interstrand side-chain pairings. (C) 1997 Academic Press Limited. [References: 60]
机译:据报道,序列RGITVNGKTYGR是不做设计肽系统的一部分。该肽折叠为β-发夹结构,每条链具有三个残基和两个残基转角。 Asn6侧链(β转角L1位的残基)似乎暴露于溶剂,仅与转角相互作用,而不与其余肽相互作用。根据蛋白质数据库的统计丰度,我们选择了该位置作为设计突变的良好候选者,这些突变应主要影响转弯稳定性,甚至可能影响链之间的配对。我们发现,所有NMR参数,特别是(CH)-H-alpha的构象位移分析和偶联常数(3)J(HNα),都具有很好的相关性,并且在所有turn突变体肽中均显示出相似的构象特征。总体估计值在所使用的不同方法之间是合理一致的。L1位置具有Asn的肽似乎是结构最完整的肽,其次是Asp6的肽。下一个结构化肽是具有Gly6的肽。人口最少的肽是带有Ala6和Ser6的肽。我们已经发现,根据蛋白质中(CH)-H-alpha的构象变化与I型β-转角β-发夹的L1位置不同残基的出现,发夹种群之间存在很强的相关性在数据库中。我们的分析表明,该肽系统足够灵敏,可以在发夹结构中记录较小的能量变化。因此,一旦开发出适当的薄板/线圈过渡算法,它就构成了量化能量贡献的适当模型。与其他研究的比较表明,特定发夹结构的设计必须包括在朗姆酒区域有利于所需转弯类型的序列,以及在链上避免其他链间侧链配对的序列。 (C)1997 Academic Press Limited。 [参考:60]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号