Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, Im Neuenhelmer Feld 253, 69120 Heidelberg, Germany.
Chemphyschem. 2009 Nov 9;10(16):2777-86. doi: 10.1002/cphc.200900581.
Since its first production from muscle tissue more than 65 years ago, our knowledge about actin has come a long way. While at the beginning it was identified as a muscle protein, nowadays actin is considered as one of the most important components of the cytoskeleton, playing a crucial role in cell motility, adhesion, morphology and intracellular transport processes. In vitro models have been constructed for about 20 years to gain better insight into the chemophysical and biomechanical properties of actin networks by being able to reduce and tune its complexity. The complexity of these models ranges from single actin filaments (F-actin) in interaction with actin-associated molecules and proteins, F-actin network gels to F-actin loaded vesicles to freely suspended F-actin networks in microfluidic environments. This review summarizes the development of F-actin network models and highlights their applicability towards step-by-step construction of complex cortex mimicking systems.
自 65 多年前首次从肌肉组织中提取以来,我们对肌动蛋白的了解已经有了很大的进展。虽然最初它被确定为一种肌肉蛋白,但如今肌动蛋白被认为是细胞骨架的最重要组成部分之一,在细胞运动、黏附、形态和细胞内运输过程中发挥着关键作用。大约 20 年来,人们构建了体外模型,通过降低和调整其复杂性,更好地了解肌动蛋白网络的物理化学和生物力学特性。这些模型的复杂性从与肌动蛋白相关分子和蛋白质相互作用的单个肌动蛋白丝(F-肌动蛋白),到 F-肌动蛋白网络凝胶,再到负载 F-肌动蛋白的囊泡,以及在微流控环境中自由悬浮的 F-肌动蛋白网络。本综述总结了 F-肌动蛋白网络模型的发展,并强调了它们在逐步构建复杂皮质模拟系统方面的适用性。