Szymanski John M, Ba Mengchen, Feinberg Adam W
Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15219, USA.
Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15219, USA.
J Mater Chem B. 2015 Oct 28;3(40):7993-8000. doi: 10.1039/C5TB01003A. Epub 2015 Aug 21.
Laminin is a cross-shaped heterotrimer composed of three polypeptides chains that assembles into an insoluble extracellular matrix (ECM) network as part of the basement membrane, serving a vital role in many processes such as embryonic development, differentiation, and muscle and nerve regeneration. Here we engineered monodisperse laminin nanofibers using a surface-initiated assembly technique in order to investigate how changes in protein composition affect formation and structure of the network. Specifically, we compared laminin 111 with varying degrees of purity and with and without entactin to determine whether these changes alter biophysical properties. All the laminin types were reproducibly patterned as 200 μm long, 20 μm wide nanofibers that were successfuly released during surface-initiated assembly into solution. All nanofibers contracted upon release, and while initial lengths were identical, lengths of released fibers depended on the laminin type. Uniquely, the laminin 111 at high purity (>95%) and without entactin spontaneouly formed helical nanofibers at greater than 90%. Atomic force microscopy revealed that the nanofiber contraction was associated with a change in nanostructure from fibrillar to nodular, suggestive of refolding of laminin molecules into a globular-like conformation. Further, for the high purity laminin that formed helices, the density of the laminin at the edges of the nanofiber was higher than in the middle, providing a possible origin for the differential pre-stress driving the helix formation. Together, these results show that variation in the purity of laminin 111 and presence of entactin can have significant impact on the biophysical properties of the assembled protein networks. This highlights the fact that our understanding of protein assembly and function is still incomplete and that cell-free, in vitro assays can provide unique insights into the ECM.
层粘连蛋白是一种十字形异源三聚体,由三条多肽链组成,作为基底膜的一部分组装成不溶性细胞外基质(ECM)网络,在胚胎发育、分化以及肌肉和神经再生等许多过程中发挥着至关重要的作用。在此,我们使用表面引发组装技术构建了单分散层粘连蛋白纳米纤维,以研究蛋白质组成的变化如何影响网络的形成和结构。具体而言,我们比较了不同纯度以及有无巢蛋白的层粘连蛋白111,以确定这些变化是否会改变生物物理性质。所有类型的层粘连蛋白都可重复地形成200μm长、20μm宽的纳米纤维,并在表面引发组装过程中成功释放到溶液中。所有纳米纤维在释放时都会收缩,虽然初始长度相同,但释放后纤维的长度取决于层粘连蛋白的类型。独特的是,高纯度(>95%)且无巢蛋白的层粘连蛋白111有超过90%会自发形成螺旋状纳米纤维。原子力显微镜显示,纳米纤维的收缩与纳米结构从纤维状到结节状的变化有关,这表明层粘连蛋白分子重新折叠成类似球状的构象。此外,对于形成螺旋的高纯度层粘连蛋白,纳米纤维边缘的层粘连蛋白密度高于中间部分,这为驱动螺旋形成的差异预应力提供了可能的来源。总之,这些结果表明层粘连蛋白111纯度的变化以及巢蛋白的存在会对组装的蛋白质网络的生物物理性质产生重大影响。这突出了一个事实,即我们对蛋白质组装和功能的理解仍然不完整,而且无细胞的体外分析可以为细胞外基质提供独特的见解。