• 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

相似文献

1
Probing endoplasmic reticulum dynamics using fluorescence imaging and photobleaching techniques.利用荧光成像和光漂白技术探究内质网动力学
Curr Protoc Cell Biol. 2013 Sep 24;60:21.7.1-21.7.29. doi: 10.1002/0471143030.cb2107s60.
2
Visualization of endoplasmic reticulum subdomains in cultured cells.培养细胞中内质网亚结构域的可视化。
J Vis Exp. 2014 Feb 18(84):e50985. doi: 10.3791/50985.
3
Photobleaching methods to study Golgi complex dynamics in living cells.用于研究活细胞中高尔基体复合体动力学的光漂白方法。
Methods Cell Biol. 2013;118:195-216. doi: 10.1016/B978-0-12-417164-0.00012-4.
4
LV-pIN-KDEL: a novel lentiviral vector demonstrates the morphology, dynamics and continuity of the endoplasmic reticulum in live neurones.LV-pIN-KDEL:一种新型慢病毒载体展示了活神经元内质网的形态、动力学和连续性。
BMC Neurosci. 2008 Jan 23;9:10. doi: 10.1186/1471-2202-9-10.
5
Translational mobility of the type 3 inositol 1,4,5-trisphosphate receptor Ca2+ release channel in endoplasmic reticulum membrane.内质网膜中3型肌醇1,4,5-三磷酸受体Ca2+释放通道的转位流动性
J Biol Chem. 2005 Feb 4;280(5):3824-31. doi: 10.1074/jbc.M409462200. Epub 2004 Nov 10.
6
Diffusional mobility of the cystic fibrosis transmembrane conductance regulator mutant, delta F508-CFTR, in the endoplasmic reticulum measured by photobleaching of GFP-CFTR chimeras.通过绿色荧光蛋白-囊性纤维化跨膜传导调节因子(GFP-CFTR)嵌合体的光漂白法测定内质网中囊性纤维化跨膜传导调节因子突变体ΔF508-CFTR的扩散迁移率。
J Biol Chem. 2002 May 10;277(19):16419-25. doi: 10.1074/jbc.M112361200. Epub 2002 Feb 27.
7
ER retention may play a role in sorting of the nuclear pore membrane protein POM121.内质网滞留可能在核孔膜蛋白POM121的分选过程中发挥作用。
Exp Cell Res. 2003 Apr 1;284(2):173-84. doi: 10.1016/s0014-4827(02)00034-4.
8
Effects of organelle shape on fluorescence recovery after photobleaching.细胞器形状对光漂白后荧光恢复的影响。
Biophys J. 2005 Sep;89(3):1482-92. doi: 10.1529/biophysj.104.057885. Epub 2005 Jun 10.
9
Imaging the secretory pathway: the past and future impact of live cell optical techniques.成像分泌途径:活细胞光学技术的过去与未来影响
Biochim Biophys Acta. 2005 Jul 10;1744(3):259-72. doi: 10.1016/j.bbamcr.2005.04.010.
10
Kar2p availability defines distinct forms of endoplasmic reticulum stress in living cells.Kar2p 的可用性决定了活细胞中内质网应激的不同形式。
Mol Biol Cell. 2012 Mar;23(5):955-64. doi: 10.1091/mbc.E11-12-0995. Epub 2012 Jan 4.

引用本文的文献

1
The photosensitive endoplasmic reticulum-chloroplast contact site.光敏内质网-叶绿体接触位点。
J Microsc. 2025 Mar;297(3):333-348. doi: 10.1111/jmi.13377. Epub 2024 Dec 4.
2
What determines sub-diffusive behavior in crowded protein solutions?是什么决定了拥挤蛋白质溶液中的亚扩散行为?
Biophys J. 2024 Jan 16;123(2):134-146. doi: 10.1016/j.bpj.2023.12.002. Epub 2023 Dec 10.
3
Protocol for quantification of the lysosomal degradation of extracellular proteins into mammalian cells.用于定量分析细胞外蛋白质在哺乳动物细胞中的溶酶体降解的方案。
STAR Protoc. 2021 Nov 23;2(4):100975. doi: 10.1016/j.xpro.2021.100975. eCollection 2021 Dec 17.
4
A novel automated image analysis pipeline for quantifying morphological changes to the endoplasmic reticulum in cultured human cells.一种新型的自动化图像分析管道,用于定量分析培养的人类细胞内质网形态变化。
BMC Bioinformatics. 2021 Sep 8;22(1):427. doi: 10.1186/s12859-021-04334-x.
5
A virtuous cycle operated by ERp44 and ERGIC-53 guarantees proteostasis in the early secretory compartment.由ERp44和ERGIC-53运作的良性循环确保早期分泌区室的蛋白质稳态。
iScience. 2021 Mar 1;24(3):102244. doi: 10.1016/j.isci.2021.102244. eCollection 2021 Mar 19.
6
Dynamic Control of Mitochondrial Ca Levels as a Survival Strategy of Cancer Cells.线粒体钙水平的动态调控作为癌细胞的一种生存策略
Front Cell Dev Biol. 2021 Feb 4;9:614668. doi: 10.3389/fcell.2021.614668. eCollection 2021.
7
QuoVadoPro, an Autonomous Tool for Measuring Intracellular Dynamics using Temporal Variance.QuoVadoPro,一种使用时间方差测量细胞内动力学的自主工具。
Curr Protoc Cell Biol. 2020 Jun;87(1):e108. doi: 10.1002/cpcb.108.
8
The Unfolded Protein Response: Detecting and Responding to Fluctuations in the Protein-Folding Capacity of the Endoplasmic Reticulum.未折叠蛋白反应:检测和响应内质网中蛋白质折叠能力的波动。
Cold Spring Harb Perspect Biol. 2019 Sep 3;11(9):a033886. doi: 10.1101/cshperspect.a033886.
9
T-Type voltage-sensitive calcium channels mediate mechanically-induced intracellular calcium oscillations in osteocytes by regulating endoplasmic reticulum calcium dynamics.T型电压敏感性钙通道通过调节内质网钙动力学介导骨细胞中机械诱导的细胞内钙振荡。
Bone. 2016 Jul;88:56-63. doi: 10.1016/j.bone.2016.04.018. Epub 2016 Apr 21.

本文引用的文献

1
ERdj3 regulates BiP occupancy in living cells.ERdj3 调控活细胞中 BiP 的占据。
J Cell Sci. 2013 Mar 15;126(Pt 6):1429-39. doi: 10.1242/jcs.118182. Epub 2013 Feb 1.
2
Rab10 GTPase regulates ER dynamics and morphology.Rab10 GTPase 调节内质网动力学和形态。
Nat Cell Biol. 2013 Feb;15(2):169-78. doi: 10.1038/ncb2647. Epub 2012 Dec 23.
3
Cysteineless non-glycosylated monomeric blue fluorescent protein, secBFP2, for studies in the eukaryotic secretory pathway.无半胱氨酸非糖基化单体蓝色荧光蛋白,secBFP2,用于真核分泌途径的研究。
Biochem Biophys Res Commun. 2013 Jan 18;430(3):1114-9. doi: 10.1016/j.bbrc.2012.12.028. Epub 2012 Dec 19.
4
Endoplasmic reticulum polymers impair luminal protein mobility and sensitize to cellular stress in alpha1-antitrypsin deficiency.内质网聚合物会损害腔蛋白的流动性,并使α1-抗胰蛋白酶缺乏症对细胞应激敏感。
Hepatology. 2013 May;57(5):2049-60. doi: 10.1002/hep.26173. Epub 2013 Mar 14.
5
Uncoupling proteostasis and development in vitro with a small molecule inhibitor of the pancreatic endoplasmic reticulum kinase, PERK.用一种小分子抑制剂胰腺内质网激酶 PERK 体外解偶联蛋白稳态和发育。
J Biol Chem. 2012 Dec 28;287(53):44338-44. doi: 10.1074/jbc.M112.428987. Epub 2012 Nov 12.
6
IRE1α cleaves select microRNAs during ER stress to derepress translation of proapoptotic Caspase-2.IRE1α 在 ER 应激过程中切割特定 microRNAs,从而解除对促凋亡 Caspase-2 的翻译抑制。
Science. 2012 Nov 9;338(6108):818-22. doi: 10.1126/science.1226191. Epub 2012 Oct 4.
7
Glycosylation is dispensable for sorting of synaptotagmin 1 but is critical for targeting of SV2 and synaptophysin to recycling synaptic vesicles.糖基化对于突触融合蛋白 1 的分拣并非必需,但对于 SV2 和突触小泡蛋白靶向再循环突触小泡却是至关重要的。
J Biol Chem. 2012 Oct 12;287(42):35658-35668. doi: 10.1074/jbc.M112.398883. Epub 2012 Aug 20.
8
The impact of the unfolded protein response on human disease.未折叠蛋白反应对人类疾病的影响。
J Cell Biol. 2012 Jun 25;197(7):857-67. doi: 10.1083/jcb.201110131.
9
Development of cysteine-free fluorescent proteins for the oxidative environment.开发用于氧化环境的不含半胱氨酸的荧光蛋白。
PLoS One. 2012;7(5):e37551. doi: 10.1371/journal.pone.0037551. Epub 2012 May 23.
10
The molecular basis for selective inhibition of unconventional mRNA splicing by an IRE1-binding small molecule.IRE1 结合小分子选择性抑制非典型 mRNA 剪接的分子基础。
Proc Natl Acad Sci U S A. 2012 Apr 10;109(15):E869-78. doi: 10.1073/pnas.1115623109. Epub 2012 Feb 6.

利用荧光成像和光漂白技术探究内质网动力学

Probing endoplasmic reticulum dynamics using fluorescence imaging and photobleaching techniques.

作者信息

Costantini Lindsey, Snapp Erik

机构信息

Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York.

出版信息

Curr Protoc Cell Biol. 2013 Sep 24;60:21.7.1-21.7.29. doi: 10.1002/0471143030.cb2107s60.

DOI:10.1002/0471143030.cb2107s60
PMID:24510787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3920296/
Abstract

This unit describes approaches and tools for studying the dynamics and organization of endoplasmic reticulum (ER) membranes and proteins in living cells using fluorescence microscopy. The ER plays a key role in secretory protein biogenesis, calcium regulation, and lipid synthesis. However, study of these processes has often been restricted to biochemical assays that average millions of lysed cells or imaging of static fixed cells. With new fluorescent protein (FP) reporter tools, sensitive commercial microscopes, and photobleaching techniques, investigators can interrogate the behaviors of ER proteins, membranes, and stress pathways in single live cells. Solutions are described for imaging challenges relevant to the ER, including the mobility of ER membranes, a range of ER structures, and the influence of post-translational modifications on FP reporters. Considerations for performing photobleaching assays for ER proteins are discussed. Finally, reporters and drugs for studying misfolded secretory protein stress and the unfolded protein response are described.

摘要

本单元介绍了利用荧光显微镜研究活细胞内质网(ER)膜和蛋白质的动力学及组织的方法和工具。内质网在分泌蛋白生物合成、钙调节和脂质合成中起关键作用。然而,这些过程的研究通常局限于对数百万裂解细胞进行平均的生化分析或对静态固定细胞的成像。借助新型荧光蛋白(FP)报告工具、灵敏的商用显微镜和光漂白技术,研究人员可以在单个活细胞中探究内质网蛋白、膜和应激途径的行为。文中描述了针对与内质网相关的成像挑战的解决方案,包括内质网膜的流动性、一系列内质网结构以及翻译后修饰对FP报告分子的影响。讨论了对内质网蛋白进行光漂白分析的注意事项。最后,介绍了用于研究错误折叠的分泌蛋白应激和未折叠蛋白反应的报告分子和药物。