• 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

Syndet is a novel SNAP-25 related protein expressed in many tissues.

作者信息

Wang G, Witkin J W, Hao G, Bankaitis V A, Scherer P E, Baldini G

机构信息

Department of Anatomy and Cell Biology, Columbia University, College of Physicians and Surgeons, New York, NY 10032, USA.

出版信息

J Cell Sci. 1997 Feb;110 ( Pt 4):505-13. doi: 10.1242/jcs.110.4.505.

DOI:10.1242/jcs.110.4.505
PMID:9067602
Abstract

SNAP-25 is a synaptosomal associated protein localized at the plasma membrane of nerve terminals. SNAP-25 associates with syntaxin 1 and vesicle-associated membrane protein-2 (VAMP-2) and is thought to form a complex essential for neurotransmitter release. We have identified syndet, a novel protein related to the family of SNAP-25 isoforms. Like SNAP-25, syndet has regions with high probability of forming coiled coils, a cysteine rich-domain, and lacks a signal sequence or transmembrane domains. Syndet is tightly bound to membranes, possibly by acylation within the cysteine-rich domain. Syndet is expressed in non-neuronal tissues. In adipocytes, syndet is found at the plasma membrane and in an intracellular compartment. The identification of syndet supports the hypothesis that multiple SNAP-25 related proteins ensure specificity of vesicle fusion at the cell surface.

摘要

相似文献

1
Syndet is a novel SNAP-25 related protein expressed in many tissues.
J Cell Sci. 1997 Feb;110 ( Pt 4):505-13. doi: 10.1242/jcs.110.4.505.
2
Identification of a novel syntaxin- and synaptobrevin/VAMP-binding protein, SNAP-23, expressed in non-neuronal tissues.在非神经组织中表达的一种新型Syntaxin和突触囊泡蛋白/囊泡相关膜蛋白结合蛋白SNAP-23的鉴定。
J Biol Chem. 1996 Jun 7;271(23):13300-3. doi: 10.1074/jbc.271.23.13300.
3
Syndet, an adipocyte target SNARE involved in the insulin-induced translocation of GLUT4 to the cell surface.Syndet是一种脂肪细胞靶向性SNARE蛋白,参与胰岛素诱导的GLUT4向细胞表面的转位过程。
J Biol Chem. 1998 Jul 24;273(30):18784-92. doi: 10.1074/jbc.273.30.18784.
4
Tissue distribution of SNAP-23 and its subcellular localization in 3T3-L1 cells.SNAP-23在3T3-L1细胞中的组织分布及其亚细胞定位。
Biochem Biophys Res Commun. 1997 Jan 3;230(1):64-8. doi: 10.1006/bbrc.1996.5884.
5
SNAP-23 participates in SNARE complex assembly in rat adipose cells.SNAP-23参与大鼠脂肪细胞中的SNARE复合体组装。
Biochem J. 1999 Mar 15;338 ( Pt 3)(Pt 3):709-15.
6
A novel tetanus neurotoxin-insensitive vesicle-associated membrane protein in SNARE complexes of the apical plasma membrane of epithelial cells.上皮细胞顶端质膜SNARE复合体中一种新型的对破伤风神经毒素不敏感的囊泡相关膜蛋白。
Mol Biol Cell. 1998 Jun;9(6):1437-48. doi: 10.1091/mbc.9.6.1437.
7
SNAP-23 and SNAP-25 are palmitoylated in vivo.SNAP - 23和SNAP - 25在体内被棕榈酰化。
Biochem Biophys Res Commun. 1999 May 10;258(2):407-10. doi: 10.1006/bbrc.1999.0652.
8
Increased association of synaptosome-associated protein of 25 kDa with syntaxin and vesicle-associated membrane protein following acrosomal exocytosis of sea urchin sperm.海胆精子顶体胞吐后,25 kDa突触体相关蛋白与 syntaxin 和囊泡相关膜蛋白的关联增加。
J Biol Chem. 1998 Sep 18;273(38):24355-9. doi: 10.1074/jbc.273.38.24355.
9
GS32, a novel Golgi SNARE of 32 kDa, interacts preferentially with syntaxin 6.GS32是一种新的32千道尔顿的高尔基体SNARE蛋白,它优先与 syntaxin 6相互作用。
Mol Biol Cell. 1999 Jan;10(1):119-34. doi: 10.1091/mbc.10.1.119.
10
Differential phosphorylation of syntaxin and synaptosome-associated protein of 25 kDa (SNAP-25) isoforms.syntaxin和25 kDa突触小体相关蛋白(SNAP-25)亚型的差异磷酸化
J Neurochem. 1999 Feb;72(2):614-24. doi: 10.1046/j.1471-4159.1999.0720614.x.

引用本文的文献

1
Gβγ-SNAP25 exocytotic brake removal enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity.去除Gβγ-SNAP25胞吐制动可增强胰岛素作用,促进脂肪细胞褐变,并预防饮食诱导的肥胖。
J Clin Invest. 2023 Oct 2;133(19):e160617. doi: 10.1172/JCI160617.
2
SNAP23 decreases insulin secretion by competitively inhibiting the interaction between SNAP25 and STX1A.突触融合蛋白 23(SNAP23)通过竞争性抑制突触融合蛋白 25(SNAP25)和 STX1A 之间的相互作用来降低胰岛素分泌。
Biosci Rep. 2023 May 31;43(5). doi: 10.1042/BSR20222594.
3
Comparative analysis of potential broad-spectrum neuronal Cre drivers.
潜在广谱神经元Cre驱动因子的比较分析
Wellcome Open Res. 2022 Jul 8;7:185. doi: 10.12688/wellcomeopenres.17965.1. eCollection 2022.
4
hiPSC-Derived Neurons Provide a Robust and Physiologically Relevant Platform to Test Botulinum Neurotoxins.人诱导多能干细胞衍生的神经元为测试肉毒杆菌神经毒素提供了一个强大且生理相关的平台。
Front Pharmacol. 2021 Jan 14;11:617867. doi: 10.3389/fphar.2020.617867. eCollection 2020.
5
Munc13 binds and recruits SNAP25 to chaperone SNARE complex assembly.Munc13 通过结合 SNAP25 将 SNARE 复合物募集到分子伴侣上。
FEBS Lett. 2021 Feb;595(3):297-309. doi: 10.1002/1873-3468.14006. Epub 2020 Dec 5.
6
The cysteine-rich domain of synaptosomal-associated protein of 23 kDa (SNAP-23) regulates its membrane association and regulated exocytosis from mast cells.突触相关蛋白 23kDa 的富含半胱氨酸结构域(SNAP-23)调节其与膜的结合以及肥大细胞中受调控的胞吐作用。
Biochim Biophys Acta Mol Cell Res. 2019 Oct;1866(10):1618-1633. doi: 10.1016/j.bbamcr.2019.06.015. Epub 2019 Jun 29.
7
Distinct Localization of SNAP47 Protein in GABAergic and Glutamatergic Neurons in the Mouse and the Rat Hippocampus.SNAP47蛋白在小鼠和大鼠海马体中GABA能神经元和谷氨酸能神经元中的独特定位
Front Neuroanat. 2017 Jul 13;11:56. doi: 10.3389/fnana.2017.00056. eCollection 2017.
8
Oxidized phagosomal NOX2 complex is replenished from lysosomes.氧化的吞噬体NOX2复合物从溶酶体中得到补充。
J Cell Sci. 2017 Apr 1;130(7):1285-1298. doi: 10.1242/jcs.196931. Epub 2017 Feb 15.
9
Opposing roles for SNAP23 in secretion in exocrine and endocrine pancreatic cells.SNAP23在胰腺外分泌细胞和内分泌细胞分泌过程中的相反作用。
J Cell Biol. 2016 Oct 10;215(1):121-138. doi: 10.1083/jcb.201604030. Epub 2016 Oct 3.
10
Drosophila SNAP-29 is an essential SNARE that binds multiple proteins involved in membrane traffic.果蝇SNAP-29是一种重要的SNARE蛋白,它能结合多种参与膜运输的蛋白质。
PLoS One. 2014 Mar 13;9(3):e91471. doi: 10.1371/journal.pone.0091471. eCollection 2014.