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Concentration-Driven Growth of Model Protocell Membranes

机译:浓度驱动模型原型细胞膜的生长

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摘要

The first protocell membranes may have assembled from fatty acids and related single-chain lipids available in the prebiotic environment. Prior to the evolution of complex cellular machinery, spontaneous protocell membrane growth and division had to result from the intrinsic physicochemical properties of these molecules, in the context of specific environmental conditions. Depending on the nature of the chemical and physical environment, fatty acids can partition between several different phases, including soluble monomers, micelles, and lamellar vesicles. Here we address the concentration dependence of fatty acid aggregation, which is dominated by entropic considerations. We quantitatively distinguish between fatty acid phases using a combination of physical and spectroscopic techniques, including the use of the fluorescent fatty acid analogue Laurdan, whose emission spectrum is sensitive to structural differences between micellar and lamellar aggregates. We find that the monomer-aggregate transition largely follows a characteristic pseudophase model of molecular aggregation but that the composition of the aggregate phase is also concentration dependent. At low amphiphile concentrations above the critical aggregate concentration, vesicles coexist with a significant proportion of micelles, while more concentrated solutions favor the lamellar vesicle phase. We subsequently show that the micelle-vesicle equilibrium can be used to drive the growth of pre-existing vesicles upon an increase in amphiphile concentration either through solvent evaporation or following the addition of excess lipids. We propose a simple model for a primitive environmentally driven cell cycle, in which protocell membrane growth results from evaporative concentration, followed by shear force or photochemically induced division.
机译:第一原始细胞膜可以由在益生元环境中可获得的脂肪酸和相关的单链脂质组装而成。在发展复杂的细胞机制之前,必须在特定的环境条件下,由这些分子的内在物理化学性质导致原生细胞膜的自发生长和分裂。取决于化学和物理环境的性质,脂肪酸可以在几个不同的相之间分配,包括可溶性单体,胶束和层状囊泡。在这里,我们解决了脂肪酸聚集的浓度依赖性,这主要是由熵引起的。我们使用物理和光谱技术的组合来定量区分脂肪酸相,包括使用荧光脂肪酸类似物Laurdan,其发射光谱对胶束和层状聚集体之间的结构差异敏感。我们发现单体-聚集体转变很大程度上遵循分子聚集的特征性假相模型,但是聚集体相的组成也与浓度有关。在高于临界聚集物浓度的低两亲物浓度下,囊泡与大量胶束共存,而更浓缩的溶液则有利于层状囊泡相。我们随后显示,通过溶剂蒸发或添加过量脂质后,两亲物浓度增加时,胶束-囊泡平衡可用于驱动预先存在的囊泡的生长。我们为原始的环境驱动的细胞周期提出了一个简单的模型,在该模型中,原始细胞膜的生长来自蒸发浓缩,然后是剪切力或光化学诱导的分裂。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第51期|20812-20819|共8页
  • 作者单位

    Howard Hughes Medical Institute, Department of Molecular Biology and Center for Computational and Integrative Biology, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, United States,Miller Institute for Basic Research in Science, University of California, Berkeley, 2536 Channing Way, Berkeley, CA 94720, USA;

    Howard Hughes Medical Institute, Department of Molecular Biology and Center for Computational and Integrative Biology, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, United States;

    Howard Hughes Medical Institute, Department of Molecular Biology and Center for Computational and Integrative Biology, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:13:41

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