• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Disordered structure and flexible roles: using the prion protein N1 fragment for neuroprotective and regenerative therapy.

作者信息

Mohammadi Behnam, Glatzel Markus, Altmeppen Hermann Clemens

机构信息

Institute of Neuropathology, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.

出版信息

Neural Regen Res. 2021 Jul;16(7):1431-1432. doi: 10.4103/1673-5374.301008.

DOI:10.4103/1673-5374.301008
PMID:33318441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8284303/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6abf/8284303/e09841c277fc/NRR-16-1431-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6abf/8284303/e09841c277fc/NRR-16-1431-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6abf/8284303/e09841c277fc/NRR-16-1431-g001.jpg

相似文献

1
Disordered structure and flexible roles: using the prion protein N1 fragment for neuroprotective and regenerative therapy.结构紊乱与灵活作用:利用朊病毒蛋白N1片段进行神经保护和再生治疗。
Neural Regen Res. 2021 Jul;16(7):1431-1432. doi: 10.4103/1673-5374.301008.
2
Transgenic Overexpression of the Disordered Prion Protein N1 Fragment in Mice Does Not Protect Against Neurodegenerative Diseases Due to Impaired ER Translocation.转染表达紊乱的朊病毒蛋白 N1 片段在小鼠中不能防止神经退行性疾病是由于内质网易位受损。
Mol Neurobiol. 2020 Jun;57(6):2812-2829. doi: 10.1007/s12035-020-01917-2. Epub 2020 May 4.
3
Expression of the Prion Protein Family Member Shadoo Causes Drug Hypersensitivity That Is Diminished by the Coexpression of the Wild Type Prion Protein.朊蛋白家族成员沙杜蛋白的表达会导致药物超敏反应,而野生型朊蛋白的共表达可减轻这种反应。
J Biol Chem. 2016 Feb 26;291(9):4473-86. doi: 10.1074/jbc.M115.679035. Epub 2015 Dec 31.
4
Identification of prion protein-derived peptides of potential use in Alzheimer's disease therapy.鉴定朊病毒蛋白衍生肽,其具有用于阿尔茨海默病治疗的潜力。
Biochim Biophys Acta Mol Basis Dis. 2018 Jun;1864(6 Pt A):2143-2153. doi: 10.1016/j.bbadis.2018.03.023. Epub 2018 Mar 28.
5
Isoform-specific contribution of protein kinase C to prion processing.蛋白激酶C对朊病毒加工的亚型特异性贡献。
Mol Cell Neurosci. 2008 Nov;39(3):400-10. doi: 10.1016/j.mcn.2008.07.013. Epub 2008 Jul 29.
6
X-ray structural and molecular dynamical studies of the globular domains of cow, deer, elk and Syrian hamster prion proteins.牛、鹿、驼鹿和叙利亚仓鼠朊病毒蛋白球状结构域的X射线结构和分子动力学研究。
J Struct Biol. 2015 Oct;192(1):37-47. doi: 10.1016/j.jsb.2015.08.014. Epub 2015 Aug 28.
7
High hydrophobic amino acid exposure is responsible of the neurotoxic effects induced by E200K or D202N disease-related mutations of the human prion protein.高疏水性氨基酸暴露是导致人类朊病毒蛋白 E200K 或 D202N 相关突变引起神经毒性作用的原因。
Int J Biochem Cell Biol. 2011 Mar;43(3):372-82. doi: 10.1016/j.biocel.2010.11.007. Epub 2010 Nov 19.
8
The effect of a membrane-mimicking environment on the interactions of Cu with an amyloidogenic fragment of chicken prion protein.模拟膜环境对铜与鸡朊蛋白淀粉样生成片段相互作用的影响。
Dalton Trans. 2017 Jun 20;46(24):7758-7769. doi: 10.1039/c7dt01069a.
9
Neuroprotective effect of flupirtine in prion disease.氟吡汀在朊病毒病中的神经保护作用。
Drugs Today (Barc). 2002 Jan;38(1):49-58. doi: 10.1358/dot.2002.38.1.660505.
10
Soluble prion protein and its N-terminal fragment prevent impairment of synaptic plasticity by Aβ oligomers: Implications for novel therapeutic strategy in Alzheimer's disease.可溶性朊蛋白及其N端片段可预防Aβ寡聚体对突触可塑性的损害:对阿尔茨海默病新型治疗策略的启示。
Neurobiol Dis. 2016 Jul;91:124-131. doi: 10.1016/j.nbd.2016.03.001. Epub 2016 Mar 3.

引用本文的文献

1
Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein.无锚风险还是释放益处?朊病毒蛋白 ADAM10 介导的脱落的最新观点。
Cell Tissue Res. 2023 Apr;392(1):215-234. doi: 10.1007/s00441-022-03582-4. Epub 2022 Jan 27.
2
Neuroprotective effect and potential of cellular prion protein and its cleavage products for treatment of neurodegenerative disorders part II: strategies for therapeutics development.神经保护作用和细胞朊病毒蛋白及其裂解产物治疗神经退行性疾病的潜力 第二部分:治疗开发策略。
Expert Rev Neurother. 2021 Sep;21(9):983-991. doi: 10.1080/14737175.2021.1965882. Epub 2021 Sep 2.

本文引用的文献

1
Transgenic Overexpression of the Disordered Prion Protein N1 Fragment in Mice Does Not Protect Against Neurodegenerative Diseases Due to Impaired ER Translocation.转染表达紊乱的朊病毒蛋白 N1 片段在小鼠中不能防止神经退行性疾病是由于内质网易位受损。
Mol Neurobiol. 2020 Jun;57(6):2812-2829. doi: 10.1007/s12035-020-01917-2. Epub 2020 May 4.
2
Prion protein N1 cleavage peptides stimulate microglial interaction with surrounding cells.朊病毒蛋白 N1 裂解肽刺激小胶质细胞与周围细胞的相互作用。
Sci Rep. 2020 Apr 20;10(1):6654. doi: 10.1038/s41598-020-63472-z.
3
Antisense oligonucleotides extend survival of prion-infected mice.
反义寡核苷酸延长朊病毒感染小鼠的存活时间。
JCI Insight. 2019 Jul 30;5(16):131175. doi: 10.1172/jci.insight.131175.
4
Identification of prion protein-derived peptides of potential use in Alzheimer's disease therapy.鉴定朊病毒蛋白衍生肽,其具有用于阿尔茨海默病治疗的潜力。
Biochim Biophys Acta Mol Basis Dis. 2018 Jun;1864(6 Pt A):2143-2153. doi: 10.1016/j.bbadis.2018.03.023. Epub 2018 Mar 28.
5
Prion protein cleavage fragments regulate adult neural stem cell quiescence through redox modulation of mitochondrial fission and SOD2 expression.朊病毒蛋白裂解片段通过氧化还原调节线粒体分裂和 SOD2 表达来调控成年神经干细胞静止。
Cell Mol Life Sci. 2018 Sep;75(17):3231-3249. doi: 10.1007/s00018-018-2790-3. Epub 2018 Mar 24.
6
The Sec61/SecY complex is inherently deficient in translocating intrinsically disordered proteins.Sec61/SecY 复合物在内在无序蛋白易位方面固有缺陷。
J Biol Chem. 2017 Dec 29;292(52):21383-21396. doi: 10.1074/jbc.M117.788067. Epub 2017 Oct 30.
7
Diverse functions of the prion protein - Does proteolytic processing hold the key?朊病毒蛋白的多种功能 - 蛋白水解加工是否是关键?
Biochim Biophys Acta Mol Cell Res. 2017 Nov;1864(11 Pt B):2128-2137. doi: 10.1016/j.bbamcr.2017.06.022. Epub 2017 Jul 8.
8
The prion protein is an agonistic ligand of the G protein-coupled receptor Adgrg6.朊病毒蛋白是G蛋白偶联受体Adgrg6的激动剂配体。
Nature. 2016 Aug 25;536(7617):464-8. doi: 10.1038/nature19312. Epub 2016 Aug 8.
9
Aβ induces its own prion protein N-terminal fragment (PrPN1)-mediated neutralization in amorphous aggregates.淀粉样β蛋白(Aβ)在无定形聚集体中诱导其自身的朊病毒蛋白N端片段(PrPN1)介导的中和作用。
Neurobiol Aging. 2014 Jul;35(7):1537-48. doi: 10.1016/j.neurobiolaging.2014.02.001. Epub 2014 Feb 6.
10
An N-terminal fragment of the prion protein binds to amyloid-β oligomers and inhibits their neurotoxicity in vivo.朊病毒蛋白的 N 端片段与淀粉样β寡聚物结合,并在体内抑制其神经毒性。
J Biol Chem. 2013 Mar 15;288(11):7857-7866. doi: 10.1074/jbc.M112.423954. Epub 2013 Jan 28.