Lynch Brian P, Hilton Al M, Simpson Garth J
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Biophys J. 2006 Oct 1;91(7):2678-86. doi: 10.1529/biophysj.106.082412. Epub 2006 Jun 23.
Dielectrophoretic force microscopy (DEPFM) and spectroscopy have been performed on individual intact surface-immobilized mammalian red blood cells. Dielectrophoretic force spectra were obtained in situ in approximately 125 ms and could be acquired over a region comparable in dimension to the effective diameter of a scanning probe microscopy tip. Good agreement was observed between the measured dielectrophoretic spectra and predictions using a single-shell cell model. In addition to allowing for highly localized dielectric characterization, DEPFM provided a simple means for noncontact imaging of mammalian blood cells under aqueous conditions. These studies demonstrate the feasibility of using DEPFM to monitor localized changes in membrane capacitance in real time with high spatial resolution on immobilized cells, complementing previous studies of mobile whole cells and cell suspensions.
已对单个完整的表面固定化哺乳动物红细胞进行了介电泳力显微镜(DEPFM)和光谱分析。介电泳力谱在约125毫秒内原位获得,并且可以在与扫描探针显微镜尖端有效直径尺寸相当的区域上采集。实测的介电泳谱与使用单壳细胞模型的预测结果之间观察到良好的一致性。除了能够进行高度局部化的介电特性表征外,DEPFM还提供了一种在水性条件下对哺乳动物血细胞进行非接触成像的简单方法。这些研究证明了使用DEPFM在固定化细胞上以高空间分辨率实时监测膜电容局部变化的可行性,补充了先前对移动全细胞和细胞悬浮液的研究。