Chemistry and Biology of Membranes and Nanoobjects, UMR5248-CNRS-Université Bordeaux-Institut Polytechnique de Bordeaux, Pessac, France.
PLoS One. 2011;6(9):e23859. doi: 10.1371/journal.pone.0023859. Epub 2011 Sep 8.
The role of phosphoinositides has been thoroughly described in many signalling and membrane trafficking events but their function as modulators of membrane structure and dynamics in membrane fusion has not been investigated. We have reconstructed models that mimic the composition of nuclear envelope precursor membranes with naturally elevated amounts of phosphoinositides. These fusogenic membranes (membrane vesicle 1(MV1) and nuclear envelope remnants (NER) are critical for the assembly of the nuclear envelope. Phospholipids, cholesterol, and polyphosphoinositides, with polyunsaturated fatty acid chains that were identified in the natural nuclear membranes by lipid mass spectrometry, have been used to reconstruct complex model membranes mimicking nuclear envelope precursor membranes. Structural and dynamic events occurring in the membrane core and at the membrane surface were monitored by solid-state deuterium and phosphorus NMR. "MV1-like" (PC∶PI∶PIP∶PIP(2), 30∶20∶18∶12, mol%) membranes that exhibited high levels of PtdIns, PtdInsP and PtdInsP(2) had an unusually fluid membrane core (up to 20% increase, compared to membranes with low amounts of phosphoinositides to mimic the endoplasmic reticulum). "NER-like" (PC∶CH∶PI∶PIP∶PIP(2), 28∶42∶16∶7∶7, mol%) membranes containing high amounts of both cholesterol and phosphoinositides exhibited liquid-ordered phase properties, but with markedly lower rigidity (10-15% decrease). Phosphoinositides are the first lipids reported to counterbalance the ordering effect of cholesterol. At the membrane surface, phosphoinositides control the orientation dynamics of other lipids in the model membranes, while remaining unchanged themselves. This is an important finding as it provides unprecedented mechanistic insight into the role of phosphoinositides in membrane dynamics. Biological implications of our findings and a model describing the roles of fusogenic membrane vesicles are proposed.
磷脂酰肌醇在许多信号转导和膜运输事件中发挥了重要作用,但它们作为调节膜结构和动力学的功能,在膜融合中尚未得到研究。我们构建了模拟核膜前体组成的模型,其中自然含有较高水平的磷酸肌醇。这些融合膜(膜小泡 1(MV1)和核膜残余物(NER)是核膜组装的关键。通过脂质质谱法在天然核膜中鉴定出的磷脂、胆固醇和多聚磷酸肌醇,以及具有多不饱和脂肪酸链的多聚磷酸肌醇,被用于构建模拟核膜前体的复杂模型膜。通过固态氘和磷 NMR 监测膜核心和膜表面发生的结构和动态事件。表现出高水平 PtdIns、PtdInsP 和 PtdInsP(2) 的“MV1 样”(PC∶PI∶PIP∶PIP(2),30∶20∶18∶12,摩尔%)膜具有异常流动的膜核心(与含有低水平磷酸肌醇的膜相比,增加了 20%,以模拟内质网)。含有高胆固醇和磷酸肌醇的“NER 样”(PC∶CH∶PI∶PIP∶PIP(2),28∶42∶16∶7∶7,摩尔%)膜表现出液晶有序相特性,但刚性明显降低(降低 10-15%)。磷酸肌醇是第一个被报道能够抵消胆固醇有序作用的脂质。在膜表面,磷酸肌醇控制模型膜中其他脂质的取向动力学,而自身保持不变。这是一个重要的发现,因为它为磷酸肌醇在膜动力学中的作用提供了前所未有的机制见解。我们的研究结果具有生物学意义,并提出了一个描述融合膜小泡作用的模型。