Barnett Samuel F H, Kanchanawong Pakorn
Mechanobiology Institute, National University of Singapore, Singapore 117411.
Department of Biomedical Engineering, National University of Singapore, Singapore 117411.
Emerg Top Life Sci. 2018 Dec 21;2(5):677-680. doi: 10.1042/ETLS20180167.
To understand how complex machines perform their functions, it is essential to map out the 'blueprints' of how their internal components are organized. Focal adhesions (FAs) are complex mechanobiological structures involved in a plethora of cell biological processes. The application of super-resolution microscopy in concert with protein engineering offers one approach to unravel the complexity of how individual proteins are organized within FAs. In our recent application, the FA protein talin was found to form a direct structural and physical link between integrin and actin. Interestingly, engineered talin constructs with alternate lengths rescaled the FA nanostructure accordingly. This helped establish that talin could be analogous to the backbone of FAs, serving as the mechanosensitive master coordinator of FA structural organization.
为了理解复杂机器如何执行其功能,勾勒出其内部组件的组织 “蓝图” 至关重要。粘着斑(FAs)是涉及众多细胞生物学过程的复杂机械生物学结构。超分辨率显微镜与蛋白质工程相结合的应用提供了一种方法来揭示单个蛋白质在粘着斑内的组织复杂性。在我们最近的应用中,发现粘着斑蛋白踝蛋白在整合素和肌动蛋白之间形成了直接的结构和物理联系。有趣的是,具有不同长度的工程化踝蛋白构建体相应地重新调整了粘着斑纳米结构的大小。这有助于确定踝蛋白可能类似于粘着斑的主干,作为粘着斑结构组织的机械敏感主协调器。