Shrestha Rebika, Cardenas Alfredo E, Elber Ron, Webb Lauren J
Department of Chemistry, ‡Institute for Cell and Molecular Biology, §Center for Nano- and Molecular Science and Technology, and ∥Institute for Computational Engineering and Sciences, The University of Texas at Austin , Austin, Texas 78712, United States.
J Phys Chem B. 2015 Feb 19;119(7):2869-76. doi: 10.1021/jp511677j. Epub 2015 Feb 4.
The magnitude of the membrane dipole field was measured using vibrational Stark effect (VSE) shifts of nitrile oscillators placed on the unnatural amino acid p-cyanophenylalanine (p-CN-Phe) added to a peptide sequence at four unique positions. These peptides, which were based on a repeating alanine-leucine motif, intercalated into small unilamellar DMPC vesicles which formed an α-helix as confirmed by circular dichroic (CD) spectroscopy. Molecular dynamics simulations of the membrane-intercalated helix containing two of the nitrile probes, one near the headgroup region of the lipid (αLAX(25)) and one buried in the interior of the bilayer (αLAX(16)), were used to examine the structure of the nitrile with respect to the membrane normal, the assumed direction of the dipole field, by quantifying both a small tilt of the helix in the bilayer and conformational rotation of the p-CN-Phe side chain at steady state. Vibrational absorption energies of the nitrile oscillator at each position showed a systematic blue shift as the nitrile was stepped toward the membrane interior; for several different concentrations of peptide, the absorption energy of the nitrile located in the middle of the bilayer was ∼3 cm(-1) greater than that of the nitrile closest to the surface of the membrane. Taken together, the measured VSE shifts and nitrile orientations within the membrane resulted in an absolute magnitude of 8-11 MV/cm for the dipole field, at the high end of the range of possible values that have been accumulated from a variety of indirect measurements. Implications for this are discussed.
通过测量添加到肽序列中四个独特位置的非天然氨基酸对氰基苯丙氨酸(p-CN-Phe)上的腈振荡器的振动斯塔克效应(VSE)位移,来测定膜偶极场的大小。这些基于重复丙氨酸-亮氨酸基序的肽插入到小单层DMPC囊泡中,圆二色性(CD)光谱证实其形成了α-螺旋。对包含两个腈探针的膜插入螺旋进行分子动力学模拟,其中一个靠近脂质的头部区域(αLAX(25)),另一个埋在双层膜内部(αLAX(16)),通过量化双层膜中螺旋的小倾斜度和稳态下p-CN-Phe侧链的构象旋转,来研究腈相对于膜法线(假定的偶极场方向)的结构。随着腈向膜内部移动,每个位置的腈振荡器的振动吸收能量呈现出系统性的蓝移;对于几种不同浓度的肽,位于双层膜中间的腈的吸收能量比最靠近膜表面的腈的吸收能量大约3 cm(-1)。综合来看,测得的VSE位移和膜内腈的取向导致偶极场的绝对大小为8 - 11 MV/cm,处于从各种间接测量积累的可能值范围的高端。本文对此进行了讨论。