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在最小合成细胞中模拟黏附

Mimicking Adhesion in Minimal Synthetic Cells.

作者信息

Bartelt Solveig M, Chervyachkova Elizaveta, Ricken Julia, Wegner Seraphine V

机构信息

Max Planck Institute of Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.

Max Planck Institute for Medical Research, Jahnstraße 29, 69120, Heidelberg, Germany.

出版信息

Adv Biosyst. 2019 Jun;3(6):e1800333. doi: 10.1002/adbi.201800333. Epub 2019 Feb 25.

Abstract

Cell adhesions to the extracellular matrix and to neighboring cells are fundamental to cell behavior and have also been implemented into minimal synthetic cells, which are assembled from molecular building blocks from the bottom-up. Investigating adhesion in cell mimetic models with reduced complexity provides a better understanding of biochemical and biophysical concepts underlying the cell adhesion machinery. In return, implementing cell-matrix and cell-cell adhesions into minimal synthetic cells allows reconstructing cell functions associated with cell adhesions including cell motility, multicellular prototissues, fusion of vesicles, and the self-sorting of different cell types. Cell adhesions have been mimicked using both the native cell receptors and reductionist mimetics providing a variety of specific, reversible, dynamic, and spatiotemporally controlled interactions. This review gives an overview of different minimal adhesion modules integrated into different minimal synthetic cells drawing inspiration from cell and colloidal science.

摘要

细胞与细胞外基质以及相邻细胞的黏附对于细胞行为至关重要,并且也已被应用于最小合成细胞中,这些最小合成细胞是由分子构建块自下而上组装而成的。在复杂性降低的细胞模拟模型中研究黏附,有助于更好地理解细胞黏附机制背后的生化和生物物理概念。反过来,将细胞-基质和细胞-细胞黏附应用于最小合成细胞,可以重建与细胞黏附相关的细胞功能,包括细胞运动、多细胞原组织、囊泡融合以及不同细胞类型的自我分选。已经使用天然细胞受体和简化模拟物来模拟细胞黏附,从而提供了各种特异性、可逆性、动态性和时空可控的相互作用。本文综述了从细胞和胶体科学中汲取灵感,整合到不同最小合成细胞中的不同最小黏附模块。

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