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两亲性α-螺旋肽在气-水界面与磷脂酰胆碱的相互作用模式。

Mode of interaction of amphiphilic alpha-helical peptide with phosphatidylcholines at the air-water interface.

作者信息

Nakahara Hiromichi, Nakamura Shohei, Hiranita Takato, Kawasaki Hideya, Lee Sannamu, Sugihara Gohsuke, Shibata Osamu

机构信息

Division of Biointerfacial Science, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

Langmuir. 2006 Jan 31;22(3):1182-92. doi: 10.1021/la0524925.

DOI:10.1021/la0524925
PMID:16430282
Abstract

Surface pressure (pi)-, surface potential (deltaV)-, and dipole moment (mu(perpendicular))-area (A) isotherms and morphological behavior were examined for monolayers of a newly designed 18-mer amphiphilic alpha-helical peptide (Hel 13-5), DPPC, and DPPC/egg-PC (1:1) and their combinations by the Wilhelmy method, ionizing electrode method, fluorescence microscopy (FM), and atomic force microscopy (AFM). The newly designed Hel 13-5 showed rapid adsorption into the air-liquid interface to form interfacial films such as a SP-B function. Regardless of the composition and constituents in their multicomponent system of DPPC/egg-PC, the collapse pressure (pi(c); approximately 42 mN m(-1)) was constant, implying that Hel 13-5 with the fluid composition of egg-PC is squeezed out of Hel 13-5/DPPC/egg-PC monolayers accompanying a two- to three-dimensional phase transformation. FM showed that adding a small amount of Hel 13-5 to DPPC induced a dispersed pattern of ordered domains with a "moth-eaten" appearance, whereas shrinkage of ordered domains in size occurred for the DPPC/egg-PC mixture with Hel 13-5. Furthermore, AFM indicated that (i) the intermediate phase was formed in pure Hel 13-5 systems between monolayer states and excluded nanoparticles, (ii) protrusions necessarily located on DPPC monolayers, and (iii) beyond the collapse pressure of Hel 13-5, Hel 13-5 was squeezed out of the system into the aqueous subphase. Furthermore, hysteresis curves of these systems nicely resemble those of the DPPC/SP-B and DPPC/SP-C mixtures reported before.

摘要

通过威尔海姆法、电离电极法、荧光显微镜(FM)和原子力显微镜(AFM),研究了新设计的18聚体两亲性α-螺旋肽(Hel 13-5)、二棕榈酰磷脂酰胆碱(DPPC)、DPPC/蛋黄卵磷脂(1:1)及其组合的单层膜的表面压力(πi)、表面电位(ΔV)、偶极矩(μ⊥)-面积(A)等温线以及形态行为。新设计的Hel 13-5迅速吸附到气液界面形成诸如表面活性蛋白B(SP-B)功能的界面膜。无论DPPC/蛋黄卵磷脂多组分体系中的组成和成分如何,其崩溃压力(πc;约42 mN m-1)是恒定的,这意味着具有蛋黄卵磷脂流体组成的Hel 13-5在伴随二维到三维相变的过程中从Hel 13-5/DPPC/蛋黄卵磷脂单层膜中被挤出。FM显示,向DPPC中添加少量Hel 13-5会诱导出具有“虫蛀”外观的有序域分散模式,而对于含有Hel 13-5的DPPC/蛋黄卵磷脂混合物,有序域尺寸会缩小。此外,AFM表明:(i)在纯Hel 13-5体系中,单层状态和排除的纳米颗粒之间形成了中间相;(ii)突起必然位于DPPC单层膜上;(iii)超过Hel 13-5的崩溃压力后,Hel 13-5被挤出体系进入水相亚层。此外,这些体系的滞后曲线与之前报道的DPPC/SP-B和DPPC/SP-C混合物的滞后曲线非常相似。

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