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蜂毒肽诱导酸性脂质体融合。

Melittin-induced fusion of acidic liposomes.

作者信息

Eytan G D, Almary T

出版信息

FEBS Lett. 1983 May 30;156(1):29-32. doi: 10.1016/0014-5793(83)80241-5.

DOI:10.1016/0014-5793(83)80241-5
PMID:6852252
Abstract

Melittin-induced fusion of acidic liposomes. Fusion was observed in the electron-microscope and assayed as intermixing of both liposomes' contents and membranes. The melittin concentrations required for fusion induction were in the microM range compared to over 10 mM Ca2+ required for a comparable effect. It is suggested that the high efficiency of melittin is due to its amphipathic nature. Its hydrophobic moiety is probably anchored in one liposome while the positively charged hydrophilic moiety attracts another liposome.

摘要

蜂毒肽诱导酸性脂质体融合。在电子显微镜下观察到融合现象,并通过脂质体内容物和膜的混合来测定。与产生类似效果所需的超过10 mM Ca2+相比,诱导融合所需的蜂毒肽浓度在微摩尔范围内。有人认为蜂毒肽的高效性归因于其两亲性。其疏水部分可能锚定在一个脂质体中,而带正电荷的亲水部分则吸引另一个脂质体。

相似文献

1
Melittin-induced fusion of acidic liposomes.蜂毒肽诱导酸性脂质体融合。
FEBS Lett. 1983 May 30;156(1):29-32. doi: 10.1016/0014-5793(83)80241-5.
2
[Interaction of melittin with model membranes: effect on the size and permeability of liposomes].[蜂毒肽与模型膜的相互作用:对脂质体大小和通透性的影响]
Ukr Biokhim Zh (1978). 1989 Sep-Oct;61(5):77-84.
3
Kinetics of melittin-induced fusion of dipalmitoylphosphatidylcholine small unilamellar vesicles.蜂毒肽诱导二棕榈酰磷脂酰胆碱小单层囊泡融合的动力学
Biochim Biophys Acta. 1987 Dec 11;905(2):494-8. doi: 10.1016/0005-2736(87)90479-2.
4
Membrane fusion activity of succinylated melittin is triggered by protonation of its carboxyl groups.琥珀酰化蜂毒肽的膜融合活性由其羧基的质子化引发。
Biochemistry. 1987 Jun 30;26(13):4056-62. doi: 10.1021/bi00387a047.
5
Phospholipases: melittin facilitation of bee venom phospholipase A2-catalyzed hydrolysis of unsonicated lecithin liposomes.磷脂酶:蜂毒溶血肽促进蜂毒磷脂酶A2催化未超声处理的卵磷脂脂质体的水解。
Arch Biochem Biophys. 1977 Sep;183(1):105-12. doi: 10.1016/0003-9861(77)90424-6.
6
Membrane fusion between liposomes composed of acidic phospholipids and neutral phospholipids induced by melittin: a differential scanning calorimetric study.蜂毒肽诱导的酸性磷脂和中性磷脂组成的脂质体之间的膜融合:差示扫描量热法研究
J Biochem. 2001 Sep;130(3):393-7. doi: 10.1093/oxfordjournals.jbchem.a002998.
7
Inhibition by melittin of phospholipid-sensitive and calmodulin-sensitive Ca2+-dependent protein kinases.蜂毒肽对磷脂敏感性和钙调蛋白敏感性钙依赖性蛋白激酶的抑制作用。
Biochem J. 1982 Jan 15;202(1):217-24. doi: 10.1042/bj2020217.
8
Melittin induces HII phase formation in cardiolipin model membranes.蜂毒肽可诱导心磷脂模型膜形成HII相。
Biochim Biophys Acta. 1987 Sep 18;903(1):142-54. doi: 10.1016/0005-2736(87)90164-7.
9
Protection by chlorpromazine, albumin and bivalent cations against haemolysis induced by melittin, [Ala-14]melittin and whole bee venom.氯丙嗪、白蛋白和二价阳离子对蜂毒肽、[丙氨酸-14]蜂毒肽和全蜂毒诱导的溶血的保护作用。
Biochem J. 1996 Aug 1;317 ( Pt 3)(Pt 3):747-54. doi: 10.1042/bj3170747.
10
Nucleation and growth of pores in 1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) / cholesterol bilayer by antimicrobial peptides melittin, its mutants and cecropin P1.抗菌肽蜂毒素及其突变体和 Cecropin P1 诱导 1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱(DMPC)/胆固醇双层中孔的成核和生长。
Colloids Surf B Biointerfaces. 2019 Jan 1;173:121-127. doi: 10.1016/j.colsurfb.2018.09.049. Epub 2018 Sep 24.

引用本文的文献

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Multiple membrane interactions and versatile vesicle deformations elicited by melittin.蜂毒素引发的多种膜相互作用和多功能囊泡变形。
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2
The lipid dependence of melittin action investigated by dual-color fluorescence burst analysis.通过双色荧光猝发分析研究蜂毒肽作用的脂质依赖性。
Biophys J. 2007 Jul 1;93(1):154-63. doi: 10.1529/biophysj.107.106005. Epub 2007 Apr 13.
3
Dynamic structure of vesicle-bound melittin in a variety of lipid chain lengths by solid-state NMR.
通过固态核磁共振研究不同脂链长度下与囊泡结合的蜂毒肽的动态结构
Biophys J. 2004 Nov;87(5):3323-35. doi: 10.1529/biophysj.104.046102. Epub 2004 Aug 31.
4
15N NMR study of the ionization properties of the influenza virus fusion peptide in zwitterionic phospholipid dispersions.在两性离子磷脂分散体系中对流感病毒融合肽电离特性的15N核磁共振研究。
Biophys J. 2000 May;78(5):2418-25. doi: 10.1016/S0006-3495(00)76785-3.
5
Stopped-flow fluorometric study of the interaction of melittin with phospholipid bilayers: importance of the physical state of the bilayer and the acyl chain length.蜂毒肽与磷脂双层相互作用的停流荧光研究:双层的物理状态和酰基链长度的重要性
Biophys J. 1995 Nov;69(5):1999-2010. doi: 10.1016/S0006-3495(95)80070-6.
6
The interaction of a synthetic mitochondrial signal peptide with lipid membranes is independent of transbilayer potential.合成线粒体信号肽与脂质膜的相互作用不依赖于跨膜电位。
EMBO J. 1987 Oct;6(10):3117-23. doi: 10.1002/j.1460-2075.1987.tb02621.x.
7
Lysozyme-induced fusion of liposomes with erythrocyte ghosts at acidic pH.溶菌酶在酸性pH条件下诱导脂质体与红细胞血影融合。
Proc Natl Acad Sci U S A. 1986 Feb;83(4):962-6. doi: 10.1073/pnas.83.4.962.
8
A chemically synthesized pre-sequence of an imported mitochondrial protein can form an amphiphilic helix and perturb natural and artificial phospholipid bilayers.一种化学合成的导入线粒体蛋白的前序列可形成两亲性螺旋,并扰乱天然和人工磷脂双层膜。
EMBO J. 1986 Jun;5(6):1327-34. doi: 10.1002/j.1460-2075.1986.tb04363.x.
9
Effect of chemical modifications of myelin basic protein on its interaction with lipid interfaces and cell fusion ability.髓鞘碱性蛋白的化学修饰对其与脂质界面相互作用及细胞融合能力的影响。
Mol Cell Biochem. 1986 May;70(2):131-9. doi: 10.1007/BF00229428.