Structural underpinnings of prion protein conversion.
作者信息
Apostol Marcin I, Surewicz Witold K
出版信息
J Biol Chem. 2011 May 27;286(21):le7; author reply Ie8. doi: 10.1074/jbc.L110.213926.
Abstract
摘要
相似文献
1
Structural underpinnings of prion protein conversion.朊病毒蛋白转化的结构基础。
J Biol Chem. 2011 May 27;286(21):le7; author reply Ie8. doi: 10.1074/jbc.L110.213926.
2
Globular domain of the prion protein needs to be unlocked by domain swapping to support prion protein conversion.朊病毒蛋白的球形结构域需要通过结构域交换来解锁，以支持朊病毒蛋白的转化。
J Biol Chem. 2011 Apr 8;286(14):12149-56. doi: 10.1074/jbc.M110.213926. Epub 2011 Feb 15.
3
UV-light exposed prion protein fails to form amyloid fibrils.暴露于紫外线的朊病毒蛋白无法形成淀粉样纤维。
PLoS One. 2008 Jul 16;3(7):e2688. doi: 10.1371/journal.pone.0002688.
4
Cyclin-dependent kinase 5 phosphorylation of familial prion protein mutants exacerbates conversion into amyloid structure.家族性朊病毒蛋白突变体的细胞周期蛋白依赖性激酶5磷酸化加剧了其向淀粉样结构的转化。
J Biol Chem. 2015 Feb 27;290(9):5759-71. doi: 10.1074/jbc.M114.630699. Epub 2015 Jan 8.
5
Copper refolding of prion protein.朊病毒蛋白的铜重折叠
Biochem Biophys Res Commun. 2000 Oct 5;276(3):1217-24. doi: 10.1006/bbrc.2000.3604.
6
Nucleated conformational conversion and the replication of conformational information by a prion determinant.核内构象转换以及由朊病毒决定簇进行的构象信息复制。
Science. 2000 Aug 25;289(5483):1317-21. doi: 10.1126/science.289.5483.1317.
7
Slow spontaneous α-to-β structural conversion in a non-denaturing neutral condition reveals the intrinsically disordered property of the disulfide-reduced recombinant mouse prion protein.在非变性中性条件下缓慢的自发α-β结构转换揭示了还原型重组小鼠朊病毒蛋白的固有无序特性。
Prion. 2012 Nov-Dec;6(5):489-97. doi: 10.4161/pri.22217. Epub 2012 Sep 17.
8
Morphology and secondary structure of stable beta-oligomers formed by amyloid peptide PrP(106-126).由淀粉样肽PrP(106 - 126)形成的稳定β - 寡聚体的形态学和二级结构
Biochemistry. 2009 Jun 30;48(25):5779-81. doi: 10.1021/bi9007319.
9
Tetracysteine-tagged prion protein allows discrimination between the native and converted forms.四半胱氨酸标记朊病毒蛋白可区分天然型和转化型。
FEBS J. 2010 May;277(9):2038-50. doi: 10.1111/j.1742-4658.2010.07619.x. Epub 2010 Mar 19.
10
Biosensing of lipid-prion interactions: insights on charge effect, Cu(II)-ions binding and prion oligomerization.脂筏相关朊病毒相互作用的生物传感：关于电荷效应、Cu(II)离子结合和朊病毒寡聚化的新见解。
Biosens Bioelectron. 2010 Dec 15;26(4):1399-406. doi: 10.1016/j.bios.2010.07.064. Epub 2010 Jul 23.
引用本文的文献
1
Prions and the potential transmissibility of protein misfolding diseases.朊病毒与蛋白质错误折叠疾病的潜在传染性。
Annu Rev Microbiol. 2013;67:543-64. doi: 10.1146/annurev-micro-092412-155735. Epub 2013 Jun 28.
本文引用的文献
1
Globular domain of the prion protein needs to be unlocked by domain swapping to support prion protein conversion.朊病毒蛋白的球形结构域需要通过结构域交换来解锁，以支持朊病毒蛋白的转化。
J Biol Chem. 2011 Apr 8;286(14):12149-56. doi: 10.1074/jbc.M110.213926. Epub 2011 Feb 15.
2
The α-helical C-terminal domain of full-length recombinant PrP converts to an in-register parallel β-sheet structure in PrP fibrils: evidence from solid state nuclear magnetic resonance.全长重组 PrP 的α-螺旋 C 端结构域在 PrP 纤维中转化为规则平行的β-折叠结构：来自固态核磁共振的证据。
Biochemistry. 2010 Nov 9;49(44):9488-97. doi: 10.1021/bi1013134.
3
Molecular architecture of human prion protein amyloid: a parallel, in-register beta-structure.人类朊病毒蛋白淀粉样蛋白的分子结构：一种平行、对齐的β结构。
Proc Natl Acad Sci U S A. 2007 Nov 27;104(48):18946-51. doi: 10.1073/pnas.0706522104. Epub 2007 Nov 19.
4
Beta-sheet core of human prion protein amyloid fibrils as determined by hydrogen/deuterium exchange.通过氢/氘交换确定的人朊病毒蛋白淀粉样纤维的β-折叠核心
Proc Natl Acad Sci U S A. 2007 Jan 30;104(5):1510-5. doi: 10.1073/pnas.0608447104. Epub 2007 Jan 22.
5
Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease.体外产生的合成朊病毒类似于散发性克雅氏病中一个新发现的PrPSc亚群。
Protein Sci. 2005 May;14(5):1222-32. doi: 10.1110/ps.041186605. Epub 2005 Mar 31.
Zotero 插件