Zhang Han, Sun Jichao, Xin Xia, Xu Wenlong, Shen Jinglin, Song Zhaohua, Yuan Shiling
Key Laboratory of Colloid and Interface Chemistry (Shandong University), Ministry of Education, Shanda nanlu No. 27, Jinan 250100, PR China.
Key Laboratory of Colloid and Interface Chemistry (Shandong University), Ministry of Education, Shanda nanlu No. 27, Jinan 250100, PR China; National Engineering Technology Research Center for Colloidal Materials, Shandong University, Shanda nanlu No. 27, Jinan 250100, PR China.
J Colloid Interface Sci. 2016 Apr 1;467:43-50. doi: 10.1016/j.jcis.2015.12.005. Epub 2015 Dec 30.
A salt-free surfactant system formed by a peptide amphiphile with short headgroup (PA,C16-GK-3) and a zwitterionic surfactant (dodecyldimethylamine oxide, C12DMAO) in water has been systematically investigated. The microstructures and properties of C16-GK-3/C12DMAO mixed system were characterized using a combination of microscopic, scattering and spectroscopic techniques, including transmission electron microscopy (TEM), field emission-scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), Fourier transform infrared (FT-IR), circular dichroism (CD) and rheological measurements. Rich phase transitions have been observed by adjusting the concentration of C16-GK-3. Investigation of the hydrogels of C16-GK-3/C12DMAO with TEM, SEM and AFM showed that all of these hydrogels form nanobelts. The nanobelt formation is performed in a hierarchical manner: β-sheet peptides and C12DMAO first interact each other to form small aggregates, which then arrange themselves to form one dimensional (1D) left-handed ribbons. The ribbons further aggregated into flat and rigid nanobelts. We proposed a mechanism to interpret the self-assembly process according to the specific peptide structure as well as multiple equilibria between the hydrogen bonding interactions between the headgroups of C16-GK-3, between C12DMAO molecules and the headgroups of C16-GK-3, chirality of the amino acid residues and hydrophobic interactions of the alkyl chains.
已对由短头基肽两亲物(PA,C16 - GK - 3)和两性离子表面活性剂(十二烷基二甲基氧化胺,C12DMAO)在水中形成的无盐表面活性剂体系进行了系统研究。使用多种微观、散射和光谱技术相结合的方法对C16 - GK - 3/C12DMAO混合体系的微观结构和性质进行了表征,这些技术包括透射电子显微镜(TEM)、场发射扫描电子显微镜(FE - SEM)、原子力显微镜(AFM)、傅里叶变换红外光谱(FT - IR)、圆二色光谱(CD)和流变学测量。通过调节C16 - GK - 3的浓度观察到了丰富的相变。用TEM、SEM和AFM对C16 - GK - 3/C12DMAO水凝胶的研究表明,所有这些水凝胶都形成了纳米带。纳米带的形成是分层次进行的:β - 折叠肽和C12DMAO首先相互作用形成小聚集体,然后这些小聚集体排列形成一维(1D)左手螺旋带。这些带进一步聚集形成扁平且刚性的纳米带。我们根据特定的肽结构以及C16 - GK - 3头基之间、C12DMAO分子之间以及C12DMAO与C16 - GK - 3头基之间的氢键相互作用、氨基酸残基的手性和烷基链的疏水相互作用之间的多重平衡,提出了一种机制来解释自组装过程。