Department of Bioengineering, Clemson University, Clemson, SC 29634, USA.
Nanotechnology. 2012 Jun 22;23(24):245705. doi: 10.1088/0957-4484/23/24/245705. Epub 2012 May 28.
Rapid phenotype characterization and identification of cultured cells, which is needed for progress in tissue engineering and drug testing, requires an experimental technique that measures physical properties of cells with sub-micron resolution. Recently, band excitation piezoresponse force microscopy (BEPFM) has been proven useful for recognition and imaging of bacteria of different types in pure water. Here, the BEPFM method is performed for the first time on physiologically relevant electrolyte media, such as Dulbecco's phosphate-buffered saline (DPBS) and Dulbecco's modified Eagle's medium (DMEM). Distinct electromechanical responses for Micrococcus lysodeikticus (Gram-positive) and Pseudomonas fluorescens (Gram-negative) bacteria in DPBS are demonstrated. The results suggest that mechanical properties of the outer surface coating each bacterium, as well as the electrical double layer around them, are responsible for the BEPFM image formation mechanism in electrolyte media.
快速的表型特征描述和培养细胞的鉴定,这是组织工程和药物测试进展所需要的,需要一种能够以亚微米分辨率测量细胞物理特性的实验技术。最近,带激发压电力显微镜(BEPFM)已被证明可用于识别和成像不同类型的纯水中的细菌。在这里,首次在生理相关的电解质介质(如 Dulbecco 的磷酸盐缓冲盐水(DPBS)和 Dulbecco 的改良 Eagle 培养基(DMEM))上进行了 BEPFM 方法。在 DPBS 中,对微球菌溶菌酶(革兰氏阳性)和荧光假单胞菌(革兰氏阴性)细菌的独特机电响应进行了证明。结果表明,每个细菌的外表面涂层的机械性能以及它们周围的双电层,是电解质介质中 BEPFM 图像形成机制的原因。