• 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

影响肌动蛋白丝和微管的毒素。

Toxins affecting actin filaments and microtubules.

作者信息

Saito Shin-ya

机构信息

Department of Pharmacology, School of Pharmaceutical Sciences, University of Shizuoka, Yada 52-1, Suruga-ku, Shizuoka 422-8526, Japan.

出版信息

Prog Mol Subcell Biol. 2009;46:187-219. doi: 10.1007/978-3-540-87895-7_7.

DOI:10.1007/978-3-540-87895-7_7
PMID:19184589
Abstract

Actin and tubulin are the two major proteins of the cytoskeleton in eukaryotic cells and both display a common property to reversibly assemble into long and flexible polymers, actin filaments and microtubules, respectively. These proteins play important roles in a variety of cellular functions and are also involved in numbers of diseases. An emerging number of marine-derived cytotoxins have been found to bind either actin or tublin, resulting in either inhibition or enhancement of polymerization. Thus, these toxins are valuable molecular probes for solving complex mechanisms of biological processes. This chapter describes actin- and tubulin-targeting marine natural products and their modes of action, with reference to their use as research tools and their clinical applications.

摘要

肌动蛋白和微管蛋白是真核细胞细胞骨架中的两种主要蛋白质,二者都具有一种共同特性,即能分别可逆地组装成细长且灵活的聚合物,即肌动蛋白丝和微管。这些蛋白质在多种细胞功能中发挥重要作用,并且还与许多疾病有关。已发现越来越多源自海洋的细胞毒素能够与肌动蛋白或微管蛋白结合,从而导致聚合作用受到抑制或增强。因此,这些毒素是用于解析生物过程复杂机制的有价值的分子探针。本章介绍了靶向肌动蛋白和微管蛋白的海洋天然产物及其作用方式,并提及了它们作为研究工具的用途及其临床应用。

相似文献

1
Toxins affecting actin filaments and microtubules.影响肌动蛋白丝和微管的毒素。
Prog Mol Subcell Biol. 2009;46:187-219. doi: 10.1007/978-3-540-87895-7_7.
2
Marine toxins and the cytoskeleton: pectenotoxins, unusual macrolides that disrupt actin.海洋毒素与细胞骨架:pectenotoxins,一类破坏肌动蛋白的特殊大环内酯类毒素
FEBS J. 2008 Dec;275(24):6082-8. doi: 10.1111/j.1742-4658.2008.06714.x. Epub 2008 Oct 24.
3
Evolution of a dynamic cytoskeleton.动态细胞骨架的演变
Philos Trans R Soc Lond B Biol Sci. 1995 Sep 29;349(1329):299-304. doi: 10.1098/rstb.1995.0117.
4
New anti-actin drugs in the study of the organization and function of the actin cytoskeleton.用于肌动蛋白细胞骨架组织与功能研究的新型抗肌动蛋白药物。
Microsc Res Tech. 1999 Oct 1;47(1):18-37. doi: 10.1002/(SICI)1097-0029(19991001)47:1<18::AID-JEMT3>3.0.CO;2-E.
5
Interference with actin dynamics is superior to disturbance of microtubule function in the inhibition of human ovarian cancer cell motility.在抑制人卵巢癌细胞运动方面,干扰肌动蛋白动力学优于扰乱微管功能。
Biochem Pharmacol. 2008 Sep 15;76(6):707-16. doi: 10.1016/j.bcp.2008.06.014. Epub 2008 Jul 2.
6
Structural basis of swinholide A binding to actin.斯氏木霉菌素A与肌动蛋白结合的结构基础。
Chem Biol. 2005 Mar;12(3):287-91. doi: 10.1016/j.chembiol.2005.02.011.
7
Marine toxins and the cytoskeleton: okadaic acid and dinophysistoxins.海洋毒素与细胞骨架:冈田酸和鳍藻毒素
FEBS J. 2008 Dec;275(24):6060-6. doi: 10.1111/j.1742-4658.2008.06711.x. Epub 2008 Oct 24.
8
Actin-targeting natural compounds as tools to study the role of actin cytoskeleton in signal transduction.靶向肌动蛋白的天然化合物作为研究肌动蛋白细胞骨架在信号转导中作用的工具。
Biochem Pharmacol. 2008 Dec 1;76(11):1310-22. doi: 10.1016/j.bcp.2008.05.028. Epub 2008 Jul 2.
9
The cytoskeleton and cell movement: general considerations.细胞骨架与细胞运动:一般考量
Methods Achiev Exp Pathol. 1979;8:1-41.
10
Diversification and specialization of the bacterial cytoskeleton.细菌细胞骨架的多样化与专业化。
Curr Opin Cell Biol. 2007 Feb;19(1):5-12. doi: 10.1016/j.ceb.2006.12.010. Epub 2006 Dec 18.

引用本文的文献

1
Nuclear-cytoplasmic asynchrony in oocyte maturation caused by TUBB8 variants via impairing microtubule function: a novel pathogenic mechanism.TUBB8 变异导致卵母细胞成熟中的核质异步,通过损害微管功能:一种新的致病机制。
Reprod Biol Endocrinol. 2023 Nov 22;21(1):109. doi: 10.1186/s12958-023-01161-y.
2
Macrolides: From Toxins to Therapeutics.大环内酯类:从毒素到治疗药物。
Toxins (Basel). 2021 May 12;13(5):347. doi: 10.3390/toxins13050347.
3
A Novel Six-Gene-Based Prognostic Model Predicts Survival and Clinical Risk Score for Gastric Cancer.
一种基于六个基因的新型预后模型预测胃癌的生存率和临床风险评分。
Front Genet. 2021 Feb 22;12:615834. doi: 10.3389/fgene.2021.615834. eCollection 2021.
4
Optogenetic Control of Spine-Head JNK Reveals a Role in Dendritic Spine Regression.光遗传学控制脊柱-JNK 揭示其在树突棘回缩中的作用。
eNeuro. 2020 Feb 20;7(1). doi: 10.1523/ENEURO.0303-19.2019. Print 2020 Jan/Feb.
5
Phenotype-Guided Natural Products Discovery Using Cytological Profiling.利用细胞图谱进行表型引导的天然产物发现
J Nat Prod. 2015 Sep 25;78(9):2242-8. doi: 10.1021/acs.jnatprod.5b00455. Epub 2015 Aug 21.
6
Biological targets and mechanisms of action of natural products from marine cyanobacteria.来自海洋蓝藻细菌的天然产物的生物学靶点及作用机制
Nat Prod Rep. 2015 Mar;32(3):478-503. doi: 10.1039/c4np00104d.
7
Largazole: from discovery to broad-spectrum therapy.拉罗塞拉:从发现到广谱治疗。
Nat Prod Rep. 2012 Apr;29(4):449-56. doi: 10.1039/c2np00066k. Epub 2012 Feb 14.
8
Bioactive substances with anti-neoplastic efficacy from marine invertebrates: Porifera and Coelenterata.来自海洋无脊椎动物(多孔动物门和腔肠动物门)的具有抗肿瘤功效的生物活性物质。
World J Clin Oncol. 2011 Nov 10;2(11):355-61. doi: 10.5306/wjco.v2.i11.355.
9
Aplysqualenol A binds to the light chain of dynein type 1 (DYNLL1).阿朴脂醇 A 与动力蛋白 1 的轻链(DYNLL1)结合。
Angew Chem Int Ed Engl. 2011 Aug 22;50(35):8134-8. doi: 10.1002/anie.201102546. Epub 2011 Jul 8.
10
Microtubule-stabilizing drugs from marine sponges: focus on peloruside A and zampanolide.海洋海绵来源的微管稳定剂药物:聚焦于佩洛里德斯 A 和赞那醇。
Mar Drugs. 2010 Mar 31;8(4):1059-79. doi: 10.3390/md8041059.