Suppr超能文献

嗜热酸菌酰基磷酸酶在单体状态和初始天然样聚集物中的结构和动力学特性。

Structural and dynamics characteristics of acylphosphatase from Sulfolobus solfataricus in the monomeric state and in the initial native-like aggregates.

机构信息

Department of Biomedical Sciences and Technologies, University of Udine, Piazzale Kolbe 4, 33100 Udine, Italy.

出版信息

J Biol Chem. 2010 May 7;285(19):14689-700. doi: 10.1074/jbc.M109.082156. Epub 2010 Mar 11.

Abstract

It has previously been shown that the acylphosphatase from Sulfolobus solfataricus is capable of forming amyloid-like aggregates under conditions in which the native structure is maintained and via the transient formation of native-like aggregates. Based on the previously determined NMR structure of the native protein, showing a ferredoxin-like fold and the peculiar presence of an unstructured N-terminal segment, we show here, at a molecular level using NMR spectroscopy, that indeed S. solfataricus acylphosphatase remains in a native-like conformation when placed in aggregating conditions and that such a native-like structure persists when the protein forms the initial aggregates, at least within the low molecular weight species. The analysis carried out under different solution conditions, based on the measurement of the combined (1)H and (15)N chemical shifts and hydrogen/deuterium exchange rates, enabled the most significant conformational changes to be monitored upon transfer of the monomeric state into aggregating conditions and upon formation of the initial native-like aggregates. Important increases of the hydrogen/deuterium exchange rates throughout the native protein, accompanied by small and localized structural changes, in the monomeric protein were observed. The results also allow the identification of the intermolecular interaction regions within the native-like aggregates, that involve, in particular, the N-terminal unstructured segment, the apical region including strands S4 and S5 with the connecting loop, and the opposite active site.

摘要

先前的研究表明,来自嗜热硫磺酸杆菌的酰基磷酸酶在维持天然结构的条件下,通过形成天然样聚集物的短暂形成,能够形成类淀粉样聚集物。基于先前确定的天然蛋白的 NMR 结构,显示出铁氧还蛋白样折叠和非结构的 N 端片段的特殊存在,我们在这里使用 NMR 光谱在分子水平上表明,当放置在聚集条件下时,嗜热硫磺酸杆菌酰基磷酸酶确实保持天然样构象,并且当蛋白质形成初始聚集物时,至少在低分子量物种中,这种天然样结构仍然存在。基于(1)H 和(15)N 化学位移和氢/氘交换率的联合测量,在不同溶液条件下进行的分析使我们能够在将单体状态转移到聚集条件下以及在形成初始天然样聚集物时监测到最显著的构象变化。在单体蛋白中,观察到整个天然蛋白的氢/氘交换率显著增加,并伴有小的局部结构变化。结果还允许识别天然样聚集物中的分子间相互作用区域,这些区域特别涉及无规卷曲的 N 端未折叠片段、包括 S4 和 S5 链和连接环的顶端区域以及相反的活性位点。

相似文献

2
A model for the aggregation of the acylphosphatase from Sulfolobus solfataricus in its native-like state.
Biochim Biophys Acta. 2008 Dec;1784(12):1986-96. doi: 10.1016/j.bbapap.2008.08.021. Epub 2008 Sep 12.
4
"Native-like aggregation" of the acylphosphatase from Sulfolobus solfataricus and its biological implications.
FEBS Lett. 2009 Aug 20;583(16):2630-8. doi: 10.1016/j.febslet.2009.07.013. Epub 2009 Jul 16.
6
Edge strand engineering prevents native-like aggregation in Sulfolobus solfataricus acylphosphatase.
FEBS J. 2014 Sep;281(18):4072-84. doi: 10.1111/febs.12861. Epub 2014 Jun 13.
7
Direct Conversion of an Enzyme from Native-like to Amyloid-like Aggregates within Inclusion Bodies.
Biophys J. 2017 Jun 20;112(12):2540-2551. doi: 10.1016/j.bpj.2017.05.011.
8
Characterizing intermolecular interactions that initiate native-like protein aggregation.
Biophys J. 2012 Jun 6;102(11):2595-604. doi: 10.1016/j.bpj.2012.03.057. Epub 2012 Jun 5.
9
The degree of structural protection at the edge beta-strands determines the pathway of amyloid formation in globular proteins.
J Am Chem Soc. 2008 Apr 2;130(13):4295-302. doi: 10.1021/ja076628s. Epub 2008 Mar 12.

引用本文的文献

1
Direct Conversion of an Enzyme from Native-like to Amyloid-like Aggregates within Inclusion Bodies.
Biophys J. 2017 Jun 20;112(12):2540-2551. doi: 10.1016/j.bpj.2017.05.011.
2
Equilibrium Ensembles for Insulin Folding from Bias-Exchange Metadynamics.
Biophys J. 2017 Apr 25;112(8):1571-1585. doi: 10.1016/j.bpj.2017.03.015.
3
Mechanisms of amyloid formation revealed by solution NMR.
Prog Nucl Magn Reson Spectrosc. 2015 Aug;88-89:86-104. doi: 10.1016/j.pnmrs.2015.05.002. Epub 2015 May 27.
4
The Tubular Sheaths Encasing Methanosaeta thermophila Filaments Are Functional Amyloids.
J Biol Chem. 2015 Aug 14;290(33):20590-600. doi: 10.1074/jbc.M115.654780. Epub 2015 Jun 24.
5
Delicate balance between functionally required flexibility and aggregation risk in a β-rich protein.
Biochemistry. 2013 Dec 10;52(49):8843-54. doi: 10.1021/bi4013462. Epub 2013 Nov 25.
6
Deletional protein engineering based on stable fold.
PLoS One. 2012;7(12):e51510. doi: 10.1371/journal.pone.0051510. Epub 2012 Dec 11.
7
Understanding protein aggregation from the view of monomer dynamics.
Mol Biosyst. 2013 Jan 27;9(1):29-35. doi: 10.1039/c2mb25334h. Epub 2012 Oct 26.
8
Characterizing intermolecular interactions that initiate native-like protein aggregation.
Biophys J. 2012 Jun 6;102(11):2595-604. doi: 10.1016/j.bpj.2012.03.057. Epub 2012 Jun 5.
9
Studying interactions by molecular dynamics simulations at high concentration.
J Biomed Biotechnol. 2012;2012:303190. doi: 10.1155/2012/303190. Epub 2012 Feb 22.
10
Selective molecular recognition in amyloid growth and transmission and cross-species barriers.
J Mol Biol. 2012 Aug 10;421(2-3):172-84. doi: 10.1016/j.jmb.2011.11.023. Epub 2011 Nov 19.

本文引用的文献

1
NMR View: A computer program for the visualization and analysis of NMR data.
J Biomol NMR. 1994 Sep;4(5):603-14. doi: 10.1007/BF00404272.
2
Amyloid formation by globular proteins under native conditions.
Nat Chem Biol. 2009 Jan;5(1):15-22. doi: 10.1038/nchembio.131.
3
A model for the aggregation of the acylphosphatase from Sulfolobus solfataricus in its native-like state.
Biochim Biophys Acta. 2008 Dec;1784(12):1986-96. doi: 10.1016/j.bbapap.2008.08.021. Epub 2008 Sep 12.
5
The degree of structural protection at the edge beta-strands determines the pathway of amyloid formation in globular proteins.
J Am Chem Soc. 2008 Apr 2;130(13):4295-302. doi: 10.1021/ja076628s. Epub 2008 Mar 12.
6
Molecular dynamics simulation suggests possible interaction patterns at early steps of beta2-microglobulin aggregation.
Biophys J. 2007 Mar 1;92(5):1673-81. doi: 10.1529/biophysj.106.098483. Epub 2006 Dec 8.
9
Protein misfolding, functional amyloid, and human disease.
Annu Rev Biochem. 2006;75:333-66. doi: 10.1146/annurev.biochem.75.101304.123901.
10
Protein quality in bacterial inclusion bodies.
Trends Biotechnol. 2006 Apr;24(4):179-85. doi: 10.1016/j.tibtech.2006.02.007. Epub 2006 Feb 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验