Matyszewska Dorota, Bilewicz Renata, Su ZhangFei, Abbasi Fatemah, Leitch J Jay, Lipkowski Jacek
Faculty of Chemistry, Biological and Chemical Research Centre, University of Warsaw , Żwirki i Wigury 101, 02089 Warsaw, Poland.
Faculty of Chemistry, University of Warsaw , ul. Pasteura 1, 02093 Warsaw, Poland.
Langmuir. 2016 Feb 23;32(7):1791-8. doi: 10.1021/acs.langmuir.5b04052. Epub 2016 Feb 11.
A phospholipid bilayer composed of 1,2-dimyristoyl-d54-sn-glycero-3-phosphocholine (d54-DMPC) was deposited onto the Au(111) electrode modified with a self-assembled monolayer of 1-thio-β-d-glucose (β-Tg) via the Langmuir-Blodgett and Langmuir-Schaefer (LB-LS) techniques. Polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) measurements were used to characterize structural and orientational changes in this model biological membrane on a hydrophilic surface modified gold electrode. The results of the spectroscopic measurements showed that the tilt angle of acyl chains obtained for deuterated DMPC bilayers supported on the β-Tg-modified gold is significantly lower than that reported previously for DMPC bilayers deposited directly on Au(111) electrodes. Moreover, tilt angles of ∼18° were obtained for d54-DMPC bilayers on β-Tg self-assembled monolayers (SAMs) at positive potentials, which are similar to the values calculated for h-DMPC deposited on bare gold in the desorbed state and to those observed for a stack of hydrated DMPC bilayers. This data confirms that the β-thioglucose SAM promotes the formation of a water cushion that separates the phospholipid bilayer from the metal surface. As a result, the DMPC polar heads are not in direct contact with the electrode and can adopt a zigzag configuration, which strengthens the chain-chain interactions and allows for an overall decrease in the tilt of the acyl chains. These novel supported model membranes may be especially useful in studies pertaining to the incorporation of peptides and proteins into phospholipid bilayers.
通过朗缪尔-布洛杰特(Langmuir-Blodgett)和朗缪尔-谢弗(Langmuir-Schaefer)(LB-LS)技术,将由1,2-二肉豆蔻酰基-d54-sn-甘油-3-磷酸胆碱(d54-DMPC)组成的磷脂双层沉积到用1-硫代-β-D-葡萄糖(β-Tg)自组装单层修饰的Au(111)电极上。采用偏振调制红外反射吸收光谱(PM-IRRAS)测量来表征该亲水性表面修饰金电极上这种模型生物膜的结构和取向变化。光谱测量结果表明,在β-Tg修饰金上支撑的氘代DMPC双层获得的酰基链倾斜角明显低于先前报道的直接沉积在Au(111)电极上的DMPC双层的倾斜角。此外,在正电位下,β-Tg自组装单层(SAMs)上的d54-DMPC双层获得了约18°的倾斜角,这与在解吸状态下沉积在裸金上的h-DMPC计算值以及观察到的水合DMPC双层堆叠的值相似。该数据证实β-硫代葡萄糖SAM促进了水垫层的形成,该水垫层将磷脂双层与金属表面分隔开。结果,DMPC极性头部不与电极直接接触,并且可以采用之字形构型,这加强了链间相互作用并使得酰基链的倾斜总体减小。这些新型支撑模型膜在与肽和蛋白质掺入磷脂双层相关的研究中可能特别有用。