Centre for Vascular Research, University of the New South Wales, Sydney, 2052 (Australia).
Chemphyschem. 2014 Mar 17;15(4):606-18. doi: 10.1002/cphc.201301041. Epub 2014 Feb 4.
Focal adhesions are complex multi-protein structures that mediate cell adhesion and cell migration in multicellular organisms. Most of the protein components involved in focal adhesion formation have been identified, but a major challenge remains: determination of the spatial and temporal dynamics of adhesion proteins in order to understand the molecular mechanisms of adhesion assembly, maturation, signal regulation, and disassembly. Progress in this field has been hampered by the limited resolution of fluorescence microscopy. Recent advances have led to the development of super-resolution techniques including single-molecule localization microscopy (SMLM). Here, we discuss how the application of these techniques has revealed important new insights into focal adhesion structure and dynamics, including the first description of the three-dimensional nano-architecture of focal adhesions and of the dynamic exchange of integrins in focal adhesions. Hence, SMLM has contributed to the refinement of existing models of adhesions as well as the establishment of novel models, thereby opening new research directions. With current improvements in SMLM instrumentation and analysis, it has become possible to study cellular adhesions at the single-molecule level.
焦点黏附是一种复杂的多蛋白结构,在多细胞生物中介导细胞黏附和细胞迁移。已经鉴定出了参与焦点黏附形成的大多数蛋白成分,但仍然存在一个主要的挑战:确定黏附蛋白的时空动态,以了解黏附组装、成熟、信号调节和解体的分子机制。该领域的进展受到荧光显微镜分辨率的限制。最近的进展导致了超分辨率技术的发展,包括单分子定位显微镜(SMLM)。在这里,我们讨论了这些技术的应用如何揭示了焦点黏附结构和动态的重要新见解,包括焦点黏附的三维纳米结构和整合素在焦点黏附中的动态交换的首次描述。因此,SMLM 有助于完善现有的黏附模型,并建立新的模型,从而开辟了新的研究方向。随着 SMLM 仪器和分析的当前改进,已经可以在单分子水平上研究细胞黏附。