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Physical Routes to Primitive Cells: An Experimental Model Based on the Spontaneous Entrapment of Enzymes inside Micrometer-Sized Liposomes

机译:原始细胞的物理途径:基于微米大小脂质体内酶自发包埋的实验模型

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摘要

How did primitive living cells originate? The formation of early cells, which were probably solute-filled vesicles capable of performing a rudimentary metabolism (and possibly self-reproduction), is still one of the big unsolved questions in origin of life. We have recently used lipid vesicles (liposomes) as primitive cell models, aiming at the study of the physical mechanisms for macromolecules encapsulation. We have reported that proteins and ribosomes can be encapsulated very efficiently, against statistical expectations, inside a small number of liposomes. Moreover the transcription-translation mixture, which realistically mimics a sort of minimal metabolic network, can be functionally reconstituted in liposomes owing to a self-concentration mechanism. Here we firstly summarize the recent advancements in this research line, highlighting how these results open a new vista on the phenomena that could have been important for the formation of functional primitive cells. Then, we present new evidences on the non-random entrapment of macromolecules (proteins, dextrans) in phospholipid vesicle, and in particular we show how enzymatic reactions can be accelerated because of the enhancement of their concentration inside liposomes.
机译:原始活细胞是如何产生的?早期细胞的形成可能是溶质充满的囊泡,能够进行基本的新陈代谢(并可能自我繁殖),但仍然是生命起源中尚未解决的主要问题之一。我们最近已使用脂质囊泡(脂质体)作为原始细胞模型,旨在研究大分子封装的物理机制。我们已经报道了蛋白质和核糖体可以非常有效地封装在少数脂质体内,这与统计预期相反。此外,由于具有自浓缩机制,实际上可模仿一种最小代谢网络的转录-翻译混合物可在脂质体中功能性重建。在这里,我们首先总结该研究领域的最新进展,重点介绍这些结果如何为可能对功能原始细胞形成重要的现象打开新的视野。然后,我们提出了关于磷脂囊泡中大分子(蛋白质,右旋糖酐)的非随机捕获的新证据,并且特别是,我们展示了由于其在脂质体中浓度的增加而可以促进酶促反应。

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