Schneider S W, Egan M E, Jena B P, Guggino W B, Oberleithner H, Geibel J P
Department of Surgery, Yale University School of Medicine, New Haven, CT 06520, USA.
Proc Natl Acad Sci U S A. 1999 Oct 12;96(21):12180-5. doi: 10.1073/pnas.96.21.12180.
Atomic force microscopy is a powerful technique used to investigate the surface of living cells under physiological conditions. The resolution of the instrument is mainly limited by the softness of living cells and the interactions with the scanning tip (cantilever). Atomic force microscopy, in combination with myosin-functionalized cantilevers, was used in the detection of ATP concentrations in solution and on living cells. Functionally active tips were used to scan the surface of cells in culture and to show that the CFTR+ cell line (S9) had a basal surface ATP concentration that could be detected with atomic force microscopy (n = 10). ATP-dependent signals were not detectable in cells scanned with noncoated or heat-inactivated enzyme-coated tips (n = 9). Enzymatically active tips may serve as a model for future development of atomic force microscopy biosensors that can simultaneously detect topographical and biologically important compounds at the surface microenvironment of living cells.
原子力显微镜是一种强大的技术,用于在生理条件下研究活细胞的表面。该仪器的分辨率主要受活细胞的柔软性以及与扫描探针(悬臂)相互作用的限制。原子力显微镜与肌球蛋白功能化的悬臂相结合,用于检测溶液中和活细胞上的ATP浓度。使用具有功能活性的探针扫描培养细胞的表面,结果表明CFTR+细胞系(S9)具有可通过原子力显微镜检测到的基础表面ATP浓度(n = 10)。在用未涂层或热灭活酶涂层的探针扫描的细胞中未检测到ATP依赖性信号(n = 9)。具有酶活性的探针可作为未来原子力显微镜生物传感器开发的模型,该生物传感器能够在活细胞的表面微环境中同时检测地形和生物学上重要的化合物。