Suppr超能文献

长短黄素氧还蛋白:II. 差异环在脱辅基黄素氧还蛋白稳定性和折叠机制中的作用。

The long and short flavodoxins: II. The role of the differentiating loop in apoflavodoxin stability and folding mechanism.

作者信息

López-Llano Jon, Maldonado Susana, Jain Shandya, Lostao Anabel, Godoy-Ruiz Raquel, Sanchez-Ruiz José M, Cortijo Manuel, Fernández-Recio Juan, Sancho Javier

机构信息

Biocomputation and Complex Systems Physics Institute, Zaragoza University, Zaragoza, Spain.

出版信息

J Biol Chem. 2004 Nov 5;279(45):47184-91. doi: 10.1074/jbc.M405791200. Epub 2004 Aug 17.

Abstract

Flavodoxins are classified in two groups according to the presence or absence of a approximately 20-residue loop of unknown function. In the accompanying paper (36), we have shown that the differentiating loop from the long-chain Anabaena PCC 7119 flavodoxin is a peripheral structural element that can be removed without preventing the proper folding of the apoprotein. Here we investigate the role played by the loop in the stability and folding mechanism of flavodoxin by comparing the equilibrium and kinetic behavior of the full-length protein with that of loop-lacking, shortened variants. We show that, when the loop is removed, the three-state equilibrium thermal unfolding of apoflavodoxin becomes two-state. Thus, the loop is responsible for the complexity shown by long-chain apoflavodoxins toward thermal denaturation. As for the folding reaction, both shortened and wild type apoflavodoxins display three-state behavior but their folding mechanisms clearly differ. Whereas the full-length protein populates an essentially off-pathway transient intermediate, the additional state observed in the folding of the shortened variant analyzed seems to be simply an alternative native conformation. This finding suggests that the long loop may also be responsible for the accumulation of the kinetic intermediate observed in the full-length protein. Most revealing, however, is that the influence of the loop on the overall conformational stability of apoflavodoxin is quite low and the natively folded shortened variant Delta(120-139) is almost as stable as the wild type protein. The fact that the loop, which is not required for a proper folding of the polypeptide, does not even play a significant role in increasing the conformational stability of the protein supports our proposal (36) that the differentiating loop of long-chain flavodoxins may be related to a recognition function, rather than serving a structural purpose.

摘要

根据是否存在一段约20个残基且功能未知的环,黄素氧还蛋白可分为两类。在随附的论文(36)中,我们已经表明,来自长链鱼腥藻PCC 7119黄素氧还蛋白的区分环是一个外围结构元件,可以去除而不影响脱辅基蛋白的正确折叠。在这里,我们通过比较全长蛋白与缺乏环的缩短变体的平衡和动力学行为,研究该环在黄素氧还蛋白的稳定性和折叠机制中所起的作用。我们表明,当去除该环时,脱辅基黄素氧还蛋白的三态平衡热解折叠变为两态。因此,该环导致长链脱辅基黄素氧还蛋白热变性表现出复杂性。至于折叠反应,缩短的和野生型脱辅基黄素氧还蛋白均表现出三态行为,但它们的折叠机制明显不同。全长蛋白形成一个基本上偏离途径的瞬时中间体,而在分析的缩短变体的折叠中观察到的额外状态似乎只是一种替代的天然构象。这一发现表明,长环也可能是全长蛋白中观察到的动力学中间体积累的原因。然而,最有启发性的是,该环对脱辅基黄素氧还蛋白整体构象稳定性的影响相当低,天然折叠的缩短变体Delta(120 - 139)几乎与野生型蛋白一样稳定。该环对于多肽的正确折叠不是必需的,甚至在增加蛋白的构象稳定性方面也不发挥重要作用,这一事实支持了我们的提议(36),即长链黄素氧还蛋白的区分环可能与识别功能有关,而不是起结构作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验