Quinn Anthony S, Rand Jacob H, Wu Xiao-Xuan, Taatjes Douglas J
Department of Pathology and Microscopy Imaging Center, College of Medicine, University of Vermont, Burlington, VT, USA.
Methods Mol Biol. 2013;931:259-93. doi: 10.1007/978-1-62703-056-4_13.
The information covered in this chapter will present a model homogenous membrane preparation technique and dynamic imaging procedure that can be successfully applied to more than one type of lipid study and atomic force microscope (AFM) instrument setup. The basic procedural steps have been used with an Asylum Research MFP-3D BIO and the Bruker (formerly, Veeco) BioScope. The AFM imaging protocol has been supplemented by procedures (not to be presented in this chapter) of ellipsometry, standardized western blotting, and dot-blots to verify appropriate purity and activity of all experimental molecular components; excellent purity and activity level of the lipids, proteins, and drug(s) greatly influence the success of imaging experiments in the scanning probe microscopy field. The major goal of the chapter is to provide detailed procedures for sample preparation and operation of the Asylum Research MFP-3D BIO AFM. In addition, one should be cognizant that our comprehensive description in the use of the MFP-3D BIO's functions for successful image acquisitions and analyses is greatly enhanced by Asylum Research's (AR's) accompanying extensive manual(s), technical notes, and AR's users forum. Ultimately, the stepwise protocol and information will allow novice personnel to begin acquiring quality images for processing and analysis with minimal supervision.
本章涵盖的信息将介绍一种模型均相膜制备技术和动态成像程序,该技术和程序可成功应用于不止一种类型的脂质研究以及原子力显微镜(AFM)仪器设置。基本程序步骤已应用于安捷伦科技的MFP-3D BIO和布鲁克(原Veeco)BioScope。AFM成像方案已通过椭圆偏振法、标准化蛋白质免疫印迹法和斑点印迹法(本章未介绍)进行补充,以验证所有实验分子成分的纯度和活性是否合适;脂质、蛋白质和药物的高纯度和活性水平对扫描探针显微镜领域成像实验的成功有很大影响。本章的主要目标是提供安捷伦科技MFP-3D BIO AFM样品制备和操作的详细程序。此外,应该认识到,安捷伦科技(AR)随附的详尽手册、技术说明以及AR用户论坛极大地增强了我们对使用MFP-3D BIO功能成功进行图像采集和分析的全面描述。最终,逐步方案和信息将使新手人员在最少监督的情况下开始获取用于处理和分析的高质量图像。