Department of Bioengineering, Stanford University, Stanford, California, USA.
Biophys J. 2010 Apr 21;98(8):1529-38. doi: 10.1016/j.bpj.2009.12.4286.
The effect of nonionic detergents of the n-alkyl-beta-D-glucopyranoside class on the ordering of lipid bilayers and the dynamics of membrane-embedded peptides were investigated with 2H- and 31P-NMR. 1,2-dipalmitoyl-sn-glycero-3-phosphocholine was selectively deuterated at methylene segments C-2, C-7, and C-16 of the two fatty acyl chains. Two trans-membrane helices, WALP-19 and glycophorin A(71-98), were synthesized with Ala-d3 in the central region of the alpha-helix. n-Alkyl-beta-D-glucopyranosides with alkyl chains with 6, 7, 8, and 10 carbon atoms were added at increasing concentrations to the lipid membrane. The bilayer structure is retained up to a detergent/lipid molar ratio of 1:1. The insertion of the detergents leads to a selective disordering of the lipids. The headgroup region remains largely unaffected; the fatty acyl chain segments parallel to the detergent alkyl chain are only modestly disordered (10-20%), whereas lipid segments beyond the methyl terminus of the detergent show a decrease of up to 50%. The change in the bilayer order profile corresponds to an increase in bilayer entropy. Insertion of detergents into the lipid bilayers is completely entropy-driven. The entropy change accompanying lipid disorder is equivalent in magnitude to the hydrophobic effect. Ala-d3 deuterated WALP-19 and GlycA(71-97) were incorporated into bilayers of 1,2-dimyristoyl-sn-glycero-3-phosphocholine at a peptide/lipid molar ratio of 1:100 and measured above the 1,2-dimyristoyl-sn-glycero-3-phosphocholine gel/liquid-crystal phase transition. Well-resolved 2H-NMR quadrupole splittings were observed for the two trans-membrane helices, revealing a rapid rotation of the CD3 methyl rotor superimposed on an additional rotation of the whole peptide around the bilayer normal. The presence of detergent fluidizes the membrane and produces magnetic alignment of bilayer domains but does not produce essential changes in the peptide conformation or dynamics.
采用 2H-NMR 和 31P-NMR 研究了非离子去污剂 n- 烷基-β-D-吡喃葡萄糖苷类对脂质双层有序性和膜嵌入肽动力学的影响。1,2-二棕榈酰-sn-甘油-3-磷酸胆碱的两条脂肪酸链的亚甲基片段 C-2、C-7 和 C-16 被选择性氘代。两个跨膜螺旋 WALP-19 和糖蛋白 A(71-98),在中心区域的 α-螺旋中用 Ala-d3 合成。将 6、7、8 和 10 个碳原子的烷基链的 n- 烷基-β-D-吡喃葡萄糖苷分别以增加的浓度添加到脂质膜中。直到去污剂/脂质摩尔比为 1:1,双层结构才得以保留。去污剂的插入导致脂质选择性无序。头基区域基本不受影响;与去污剂烷基链平行的脂肪酸链段只有适度无序(10-20%),而去污剂甲基端以外的脂质段则减少高达 50%。双层有序性谱的变化对应于双层熵的增加。去污剂插入脂质双层完全是熵驱动的。伴随脂质无序的熵变化与疏水效应相当。Ala-d3 氘代 WALP-19 和 GlycA(71-97)以肽/脂质摩尔比 1:100 掺入 1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱的双层中,并在 1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱凝胶/液晶相转变之上进行测量。两个跨膜螺旋观察到了很好分辨的 2H-NMR 四极分裂,表明 CD3 甲基转子的快速旋转叠加在整个肽围绕双层法线的额外旋转上。去污剂使膜流动并产生双层域的磁取向,但不会对肽构象或动力学产生本质变化。