Nicholas Matthew P, Rao Lu, Gennerich Arne
Department of Anatomy and Structural Biology, Gruss Lipper Biophotonics Center, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY, 10461, USA.
Methods Mol Biol. 2014;1136:137-69. doi: 10.1007/978-1-4939-0329-0_9.
Rigid attachment of microtubules (MTs) to glass cover slip surfaces is a prerequisite for a variety of microscopy experiments in which MTs are used as substrates for MT-associated proteins, such as the molecular motors kinesin and cytoplasmic dynein. We present an MT-surface coupling protocol in which aminosilanized glass is formylated using the cross-linker glutaraldehyde, fluorescence-labeled MTs are covalently attached, and the surface is passivated with highly pure beta-casein. The technique presented here yields rigid MT immobilization while simultaneously blocking the remaining glass surface against nonspecific binding by polystyrene optical trapping microspheres. This surface chemistry is straightforward and relatively cheap and uses a minimum of specialized equipment or hazardous reagents. These methods provide a foundation for a variety of optical tweezers experiments with MT-associated molecular motors and may also be useful in other assays requiring surface-immobilized proteins.
微管(MTs)与玻璃盖玻片表面的牢固附着是各种显微镜实验的前提条件,在这些实验中,MTs被用作与MT相关蛋白(如分子马达驱动蛋白和细胞质动力蛋白)的底物。我们提出了一种MT-表面偶联方案,其中氨基硅烷化玻璃使用交联剂戊二醛进行甲酰化,荧光标记的MTs共价附着,并且表面用高纯度β-酪蛋白进行钝化。这里介绍的技术可实现MT的牢固固定,同时阻止剩余的玻璃表面被聚苯乙烯光镊微球非特异性结合。这种表面化学方法简单且相对便宜,并且使用最少的专用设备或危险试剂。这些方法为各种使用与MT相关的分子马达的光镊实验奠定了基础,也可能对其他需要表面固定蛋白的检测有用。