Han X, Steinhauer D A, Wharton S A, Tamm L K
Department of Molecular Physiology and Biological Physics and Center for Structural Biology, University of Virginia Health Sciences Center, Box 10011, Charlottesville, Virginia 22906-0011, USA.
Biochemistry. 1999 Nov 9;38(45):15052-9. doi: 10.1021/bi991232h.
The amino-terminal region of the membrane-anchored subunit of influenza virus hemagglutinin, the fusion peptide, is crucial for membrane fusion of this virus. The peptide is extruded from the interior of the protein and inserted into the lipid bilayer of the target membrane upon induction of a conformational change in the protein by low pH. Although the effects of several mutations in this region on the fusion behavior and the biophysical properties of the corresponding peptides have been studied, the structural requirements for an active fusion peptide have still not been defined. To probe the sensitivity of the fusion peptide structure and function to small hydrophobic perturbations in the middle of the hydrophobic region, we have individually replaced the alanine residues in positions 5 and 7 with smaller (glycine) or bulkier (valine) hydrophobic residues and measured the extent of fusion mediated by these hemagglutinin constructs as well as some biophysical properties of the corresponding synthetic peptides in lipid bilayers. We find that position 5 tolerates a smaller and position 7 a larger hydrophobic side chain. All peptides contained segments of alpha-helical (33-45%) and beta-strand (13-16%) conformation as determined by CD and ATR-FTIR spectroscopy. The order parameters of the peptide helices and the lipid hydrocarbon chains were determined from measurements of the dichroism of the respective infrared absorption bands. Order parameters in the range of 0.0-0.6 were found for the helices of these peptides, which indicate that these peptides are most likely aligned with their alpha-helices at oblique angles to the membrane normal. Some (mostly fusogenic) peptides induced significant increases of the order parameter of the lipid hydrocarbon chains, suggesting that the lipid bilayer becomes more ordered in the presence of these peptides, possibly as a result of dehydration at the membrane surface.
流感病毒血凝素膜锚定亚基的氨基末端区域,即融合肽,对于该病毒的膜融合至关重要。在低pH诱导蛋白质构象变化时,该肽从蛋白质内部挤出并插入靶膜的脂质双层中。尽管已经研究了该区域中几个突变对融合行为和相应肽的生物物理性质的影响,但活性融合肽的结构要求仍未明确。为了探究融合肽结构和功能对疏水区域中间小的疏水扰动的敏感性,我们分别用较小的(甘氨酸)或较大的(缬氨酸)疏水残基取代了第5和第7位的丙氨酸残基,并测量了这些血凝素构建体介导的融合程度以及脂质双层中相应合成肽的一些生物物理性质。我们发现第5位能够耐受较小的疏水侧链,而第7位能够耐受较大的疏水侧链。通过圆二色光谱(CD)和衰减全反射傅里叶变换红外光谱(ATR-FTIR)测定,所有肽都含有α-螺旋(33-45%)和β-链(13-16%)构象的片段。肽螺旋和脂质烃链的序参数通过测量各自红外吸收带的二色性来确定。这些肽的螺旋的序参数在0.0-0.6范围内,这表明这些肽的α-螺旋很可能以与膜法线成倾斜角度的方式排列。一些(大多是促融合的)肽导致脂质烃链的序参数显著增加,这表明在这些肽存在的情况下脂质双层变得更加有序,可能是由于膜表面脱水的结果。