Parsons M, Vojnovic B, Ameer-Beg S
Randall Centre, New Hunts House, Kings College London, Guys Campus, London SE1 1UL, UK.
Biochem Soc Trans. 2004 Jun;32(Pt3):431-3. doi: 10.1042/BST0320431.
Protein-protein interactions and signal transduction pathways have traditionally been analysed using biochemical techniques or standard microscopy. Although invaluable in the delineation of protein hierarchy, these methods do not provide information on the true spatial and temporal nature of complex formation within the intact cell. Recent advances in microscopy have allowed the development of new methods to analyse protein-protein interactions at very high resolution in both fixed and live cells. The present paper provides a brief overview of using fluorescence resonance energy transfer to analyse directly molecular interactions and conformational changes in various proteins involved in the regulation of cell adhesion and motility.
蛋白质-蛋白质相互作用和信号转导通路传统上是使用生化技术或标准显微镜进行分析的。尽管这些方法在描绘蛋白质层级方面非常宝贵,但它们无法提供关于完整细胞内复合物形成的真实空间和时间性质的信息。显微镜技术的最新进展使得开发新方法成为可能,能够在固定细胞和活细胞中以非常高的分辨率分析蛋白质-蛋白质相互作用。本文简要概述了利用荧光共振能量转移直接分析参与细胞黏附和运动调节的各种蛋白质中的分子相互作用和构象变化。