Suppr超能文献

磷脂组成对两亲性肽介导的双层囊泡中孔形成的影响。

Effect of phospholipid composition on an amphipathic peptide-mediated pore formation in bilayer vesicles.

作者信息

Nicol F, Nir S, Szoka F C

机构信息

School of Pharmacy, University of California, San Francisco, California 94143-0446, USA.

出版信息

Biophys J. 2000 Feb;78(2):818-29. doi: 10.1016/S0006-3495(00)76639-2.

Abstract

To better understand the influence of phospholipid acyl-chain composition on the formation of pores by cytotoxic amphipathic helices in biological membranes, the leakage of aqueous contents induced by the synthetic peptide GALA (WEAALAEALAE ALAEHLAEALAEALEALAA) from large unilamellar phospholipid vesicles of various compositions has been studied. Peptide-mediated leakage was examined at pH 5.0 from vesicles made of phosphatidylcholine (PC) and phosphatidylglycerol (PG) with the following acyl-chain compositions: 1-palmitoyl-2-oleoyl (PO), 1,2-dioleoyl (DO), 1, 2-dielaidoyl (DE), and 1,2-dipetroselinoyl (DPe). A mathematical model predicts and simulates the final extents of GALA-mediated leakage of 1-aminonaphthalene-3,6,8-trisulfonic acid (ANTS) and p-xylene-bis-pyridinium bromide (DPX) from 1-palmitoyl-2-oleoyl-phosphatidylcholine/1-palmitoyl-2-oleoyl-phospha tidylglycerol (POPC/POPG) and 1, 2-dielaidoyl-sn-glycero-3-phosphocholine/1, 2-dielaidoyl-phosphatidylglycerol (DEPC/DEPG) liposomes at pH 5.0 as a function of peptide concentration in the bilayer, by considering that GALA pores responsible for this leakage have a minimum size of 10 +/- 2 monomers and are formed by quasiirreversible aggregation of the peptide. With the phospholipid acyl-chain compositions tested, GALA-induced ANTS/DPX leakage follows the rank order POPC/POPG approximately DEPC/DEPG > DPePC/DPePG > DOPC/DOPG. Results from binding experiments reveal that this reduced leakage from DOPC/DOPG vesicles cannot be explained by a reduced binding affinity of the peptide to these membranes. As shown by monitoring the leakage of a fluorescent dextran, an increase in the minimum pore size also does not explain the reduction in ANTS/DPX leakage. The data suggest that surface-associated GALA monomers or aggregates are stabilized in bilayers composed of phospholipids containing a cis unsaturation per acyl chain (DO and DPe), while transbilayer peptide insertion is reduced. GALA-induced ANTS/DPX leakage is also decreased when the vesicles contain phosphatidylethanolamine (PE). This lends further support to the suggestion that factors stabilizing the surface state of the peptide reduce its insertion and subsequent pore formation in the bilayer.

摘要

为了更好地理解磷脂酰基链组成对生物膜中细胞毒性两亲性螺旋形成孔的影响,研究了合成肽GALA(WEAALAEALAE ALAEHLAEALAEALEALAA)从各种组成的大单层磷脂囊泡中诱导的水相内容物泄漏情况。在pH 5.0条件下,检测了由磷脂酰胆碱(PC)和磷脂酰甘油(PG)制成的、具有以下酰基链组成的囊泡的肽介导泄漏情况:1-棕榈酰-2-油酰(PO)、1,2-二油酰(DO)、1,2-二反油酰(DE)和1,2-二岩芹酰(DPe)。一个数学模型预测并模拟了在pH 5.0时,1-氨基萘-3,6,8-三磺酸(ANTS)和对二甲苯双溴化吡啶鎓(DPX)从1-棕榈酰-2-油酰磷脂酰胆碱/1-棕榈酰-2-油酰磷脂酰甘油(POPC/POPG)和1,2-二反油酰-sn-甘油-3-磷酸胆碱/1,2-二反油酰磷脂酰甘油(DEPC/DEPG)脂质体中通过GALA介导的泄漏最终程度,该模型考虑到导致这种泄漏的GALA孔具有最小尺寸为10±2个单体,并且是由肽的准不可逆聚集形成的。在所测试的磷脂酰基链组成中,GALA诱导的ANTS/DPX泄漏遵循以下顺序:POPC/POPG≈DEPC/DEPG>DPePC/DPePG>DOPC/DOPG。结合实验结果表明,DOPC/DOPG囊泡泄漏减少不能用肽与这些膜的结合亲和力降低来解释。如通过监测荧光葡聚糖的泄漏所示,最小孔径的增加也不能解释ANTS/DPX泄漏的减少。数据表明,表面相关的GALA单体或聚集体在由每个酰基链含有顺式不饱和键的磷脂(DO和DPe)组成的双层中稳定,而跨膜肽插入减少。当囊泡含有磷脂酰乙醇胺(PE)时,GALA诱导的ANTS/DPX泄漏也会减少。这进一步支持了这样的观点,即稳定肽表面状态的因素会减少其在双层中的插入及随后的孔形成。

相似文献

5
Membrane binding and insertion of the predicted transmembrane domain of human scramblase 1.人磷脂翻转酶1预测跨膜结构域的膜结合与插入
Biochim Biophys Acta. 2014 Jan;1838(1 Pt B):388-97. doi: 10.1016/j.bbamem.2013.09.018. Epub 2013 Oct 4.

引用本文的文献

5
Mechanistic Landscape of Membrane-Permeabilizing Peptides.膜渗透肽的作用机制全景
Chem Rev. 2019 May 8;119(9):6040-6085. doi: 10.1021/acs.chemrev.8b00520. Epub 2019 Jan 9.
10
Coupled folding and specific binding: fishing for amphiphilicity.耦合折叠与特异性结合:探寻两亲性
Int J Mol Sci. 2011;12(3):1431-50. doi: 10.3390/ijms12031431. Epub 2011 Feb 24.

本文引用的文献

6
8
Pore formation and translocation of melittin.蜂毒肽的孔形成与转位。
Biophys J. 1997 Aug;73(2):831-8. doi: 10.1016/S0006-3495(97)78115-3.

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