Centre for Protolife Research, Centre for Organized Matter Chemistry, School of Chemistry, University of Bristol, Bristol BS8 1TS, UK.
Centre for Protolife Research, Centre for Organized Matter Chemistry, School of Chemistry, University of Bristol, Bristol BS8 1TS, UK.
Curr Opin Chem Biol. 2014 Oct;22:1-11. doi: 10.1016/j.cbpa.2014.05.018. Epub 2014 Jun 19.
This review discusses recent advances in the design and construction of protocell models based on the self-assembly or microphase separation of non-lipid building blocks. We focus on strategies involving partially hydrophobic inorganic nanoparticles (colloidosomes), protein-polymer globular nano-conjugates (proteinosomes), amphiphilic block copolymers (polymersomes), and stoichiometric mixtures of oppositely charged biomolecules and polyelectrolytes (coacervates). Developments in the engineering of membrane functionality to produce synthetic protocells with gated responses and control over multi-step reactions are described. New routes to protocells comprising molecularly crowded, cytoskeletal-like hydrogel interiors, as well as to the construction of hybrid protocell models are also highlighted. Together, these strategies enable a wide range of biomolecular and synthetic components to be encapsulated, regulated and processed within the micro-compartmentalized volume, and suggest that the development of non-lipid micro-ensembles offers an approach that is complementary to protocell models based on phospholipid or fatty acid vesicles.
本文综述了近年来基于非脂质构建基元的自组装或微相分离构建原细胞模型的最新进展。我们重点讨论了涉及部分疏水性无机纳米粒子(胶体囊泡)、蛋白-聚合物球形纳米缀合物(蛋白囊泡)、两亲性嵌段共聚物(聚合物囊泡)和带相反电荷的生物分子和聚电解质的化学计量混合物(凝聚物)的策略。描述了用于产生具有门控响应和控制多步反应的合成原细胞的膜功能工程的新进展。还强调了包含分子拥挤的、细胞骨架样水凝胶内部的原细胞以及构建杂交原细胞模型的新途径。这些策略使各种生物分子和合成成分能够在微分隔体积内被封装、调节和处理,并表明非脂质微组装的发展提供了一种与基于磷脂或脂肪酸囊泡的原细胞模型互补的方法。