Serwer P, Hayes S J, Griess G A
Anal Biochem. 1986 Feb 1;152(2):339-45. doi: 10.1016/0003-2697(86)90419-7.
Electrophoresis in an agarose gel dilute enough to be almost nonretarding, followed by electrophoresis in an orthogonal direction into a more concentrated agarose gel, has been developed as a procedure to determine the radius of spherical particles. Unlike procedures of unidirectional electrophoresis in a single gel, the above procedure can be used to compare the radii of particles that differ in solid-support-free electrophoretic mobility. Accuracy of 0.3 nm has been achieved with particles 30 nm in radius. It was found that the apparent radius of the spherical capsid of bacteriophage P22 decreased by 3% during elevated temperature-induced ejection of DNA from the capsid. Though originally designed for use with multimolecular particles, the procedure described here should also be useful with monomolecular particles.
在足够稀以至于几乎没有阻滞作用的琼脂糖凝胶中进行电泳,然后在正交方向上进入浓度更高的琼脂糖凝胶中进行电泳,这一方法已被开发用于测定球形颗粒的半径。与在单一凝胶中进行单向电泳的方法不同,上述方法可用于比较在无固相支持物的电泳迁移率上存在差异的颗粒的半径。对于半径为30nm的颗粒,已实现了0.3nm的精度。研究发现,在高温诱导噬菌体P22的衣壳DNA释放过程中,其球形衣壳的表观半径减小了3%。尽管该方法最初设计用于多分子颗粒,但这里描述的方法对单分子颗粒也应该有用。