Brosius B, Riesner D
Universität Düsseldorf, Institut für Physikalische Biologie, FRG.
J Biomol Struct Dyn. 1986 Oct;4(2):271-90. doi: 10.1080/07391102.1986.10506346.
The conformational transitions of nucleic acids which were enclosed in reverse phase evaporation vesicles (REV) were studied by thermal denaturation with optical recording. Cloned fragments of double-stranded DNA containing 179 base pairs and 187 base pairs, respectively, and polyA.polyU were enclosed in REV with a yield up to every vesicle containing 50 nucleic acid molecules. With the 179 base pairs DNA enclosed in the vesicle from egg lecithin two well resolved helix-coil transitions could be measured; one is very similar in the midpoint-temperature Tm and halfwidth delta T1/2 to the transition of the free nucleic acid, and the other transition occurs stabilized at a 3.5 degrees C higher Tm-value and with a broader delta T1/2, 2.7 degrees C instead of 0.6 degree C. Both transitions are from nucleic acids inside the vesicles. Varying the surface charge of the lipid membrane by adding the negatively charged phosphatidylserine or phosphatidylglycerol, an optimum in the yield of enclosure and a maximum in the increase in Tm (4.5 degrees C) and delta T1/2 (5.5 degrees C instead of 1.0 degrees C) was obtained at 20% phosphatidylserine or phosphatidylglycerol. In vesicles from pure negatively charged lipids no second population of nucleic acids was observed. Qualitatively, similar effects were observed with polyA.polyU. Stabilization and broadening of the second transition is higher for nucleic acids inside vesicles from lipids with unsaturated fatty acids, as dioleoyl-phosphatidylcholine, than with saturated fatty acids, dipalmitoyl-phosphatidylcholine. Stabilization and broadening decrease with increasing ionic strength, whereas the relative contributions of both transitions to the total hypochromicity remain unchanged; the second transition coincides with the first at 90 mM Na+. From the experimental results it was concluded that the interaction of nucleic acids and lipid membranes is mainly of electrostatic nature. The nucleic acids exist inside the vesicles in two populations, one behaving like nucleic acid free in solution and one influenced by the contact with the membrane. All results are in accordance with a model in which the interaction between the nucleic acid and the membrane is in competition with the dipole-dipole interaction inside the membrane surface.
采用光学记录热变性法研究了包裹于反相蒸发囊泡(REV)中的核酸的构象转变。分别含有179个碱基对和187个碱基对的双链DNA克隆片段以及聚腺苷酸 - 聚尿苷酸被包裹于REV中,产率高达每个囊泡含有50个核酸分子。对于由卵磷脂形成的囊泡中包裹的179个碱基对的DNA,可以测量到两个分辨良好的螺旋 - 线圈转变;一个在中点温度Tm和半峰宽ΔT1/2方面与游离核酸的转变非常相似,另一个转变在高3.5℃的Tm值且具有更宽的ΔT1/2(2.7℃而非0.6℃)时稳定发生。这两个转变均来自囊泡内部的核酸。通过添加带负电荷的磷脂酰丝氨酸或磷脂酰甘油来改变脂质膜的表面电荷,在20%磷脂酰丝氨酸或磷脂酰甘油时获得了包裹产率的最佳值以及Tm增加的最大值(4.5℃)和ΔT1/2增加的最大值(5.5℃而非1.0℃)。在由纯带负电荷的脂质形成的囊泡中未观察到第二群核酸。定性地说,聚腺苷酸 - 聚尿苷酸也观察到了类似的效应。与含有饱和脂肪酸(如二棕榈酰磷脂酰胆碱)的脂质形成的囊泡相比,来自含有不饱和脂肪酸(如二油酰磷脂酰胆碱)的脂质形成的囊泡内部的核酸,其第二个转变的稳定化和展宽程度更高。稳定化和展宽程度随离子强度增加而降低,而两个转变对总减色性的相对贡献保持不变;在90 mM Na +时第二个转变与第一个转变重合。从实验结果得出结论,核酸与脂质膜的相互作用主要是静电性质的。核酸在囊泡内部以两种群体存在,一种表现得像溶液中游离的核酸,另一种受到与膜接触的影响。所有结果都符合一个模型,即核酸与膜之间的相互作用与膜表面内部的偶极 - 偶极相互作用相互竞争。