Mona Krompers, Miriam Jaki, Sinja Götz, Jan Lembeck, Laurine Kaul, Martin Holzer and Heiko Heerklotz
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引用次数: 0
Abstract
Biomembranes show asymmetric lipid composition of their two leaflets. The phenomenon that ordered domains in one leaflet may affect the order of the other has been referred to as interleaflet coupling and discussed in terms of transmembrane signaling. Many coupling mechanisms have been proposed; one potential mechanism should arise from the fact that the isolated melting of an ordered, e.g., gel phase gives rise to a significant expansion of this leaflet, resulting in a mismatch between the intrinsic areas of the leaflets. This asymmetry stress can be accommodated in a number of ways. One is interleaflet coupling – individually higher- and lower-melting leaflets melt together at intermediate melting temperature. Alternatively, the membrane may bend towards the larger-intrinsic-area leaflet, bud and release very small daughter vesicles (DVs). Here, we prepared lipid-asymmetric large unilamellar vesicles (aLUVs) with low-melting stearyl-oleyl-phosphatidylcholine (SOPC) in the inner and SOPC with ∼20 mol% of high-melting dipalmitoyl phosphatidylglycerol (DPPG) in the outer leaflet. Phase transitions in aLUVs versus LUVs were recorded with pressure perturbation calorimetry; vesicle budding was monitored by asymmetric flow field-flow fractionation (AF4) and visualized by cryo-transmission electron microscopy. An HPLC protocol was established to quantify the total DPPG content; zeta potential was used to detect outer-leaflet DPPG. It turned out to be possible to prepare aLUVs at 5 and 15 °C, with the outer leaflet partially in the gel phase. The properties of the final aLUVs depended on the preparation temperature. aLUVs prepared at 5 and 15 °C caused the budding of exovesicles upon heating and only weak coupling of the phase transitions of the leaflets. aLUVs prepared at 30 °C with both leaflets in the fluid state showed stronger coupling upon asymmetric freezing/melting at lower temperature. This is in line with the hypotheses that (i) the exchange of lipid between close-to lipid-saturated cyclodextrin and acceptor vesicles at a given temperature results in largely stress-free bilayers and (ii) that outside budding and coupling are, to some extent, alternative responses of the bilayer to asymmetric expansion. These hypotheses help explaining our and some literature data; the overall understanding and prediction of coupling for any given aLUV system remains an urgent, open question.
生物膜的两个小叶的脂质组成不对称。一个单叶中的有序结构域可能影响另一个单叶的有序结构域的现象被称为单叶间偶联,并在跨膜信号传导方面进行了讨论。人们提出了许多耦合机制;一种潜在的机制应该源于这样一个事实,即有序相(例如凝胶相)的孤立熔化会导致小叶的显著膨胀,从而导致小叶固有区域之间的不匹配。这种不对称应力可以通过多种方式加以调节。一种是小叶间耦合——在中等熔化温度下,高熔点和低熔点的小叶单独熔化在一起。或者,膜可能向较大的本征面积的小叶、芽弯曲,并释放非常小的子囊泡(DVs)。在这里,我们用低熔点的硬脂酰磷脂酰胆碱(SOPC)在内部制备了脂质不对称的大单层囊泡(aLUVs), SOPC在外部小叶中加入了约20摩尔%的高熔点双棕榈酰磷脂酰甘油(DPPG)。用压力摄动量热法记录aLUVs vs LUVs的相变;采用不对称流场-流分选法(AF4)监测囊泡出芽,并用低温透射电镜观察。建立HPLC法定量测定DPPG总含量;zeta电位检测外叶DPPG。结果证明,在5°C和15°C下制备aluv是可能的,其中外层小叶部分处于凝胶相。最终制备的aluv的性能取决于制备温度。在5°C和15°C制备的aluv在加热时引起外囊泡的出芽,并且小叶的相变只有弱耦合。在30℃条件下制备的aLUVs,在较低的温度下,两个小叶都处于流体状态,在不对称冻结/融化过程中表现出更强的耦合性。这与以下假设一致:(i)在给定温度下,接近脂饱和的环糊精和受体囊泡之间的脂质交换导致双分子层在很大程度上无应力;(ii)在某种程度上,外出芽和偶联是双分子层对不对称膨胀的替代反应。这些假设有助于解释我们和一些文献数据;对任何给定aLUV系统的耦合的全面理解和预测仍然是一个紧迫的、悬而未决的问题。