Huang S, Hayes S J, Serwer P
Department of Biochemistry, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229-3900, USA.
J Struct Biol. 2001 Sep;135(3):270-80. doi: 10.1006/jsbi.2001.4412.
To build a foundation for the single-molecule fluorescence microscopy of protein complexes, the present study achieved fluorescence microscopy of single, nucleic acid-free protein capsids of bacteriophage T7. The capsids were stained with Alexa 488 (green emission). Manipulation of the capsids' thermal motion was achieved in three dimensions. The procedure for manipulation included embedding the capsids in an agarose gel. The data indicate that the thermal motion of capsids is reduced by the sieving of the gel. The thermal motion can be reduced to any desired level. A semilogarithmic plot of an effective diffusion constant as a function of gel concentration is linear. Single, diffusing T7 capsids were also visualized in the presence of single DNA molecules that had been both stretched and immobilized by gel-embedding. The DNA molecules were stained with ethidium (orange emission). This study shows that single-molecule (protein and DNA) analysis is possible for both packaging of DNA in a bacteriophage capsid and other events of DNA metabolism. The major problem is the maintenance of biochemical activity.
为了为蛋白质复合物的单分子荧光显微镜技术奠定基础,本研究实现了对噬菌体T7无核酸的单个蛋白质衣壳的荧光显微镜观察。衣壳用Alexa 488(绿色荧光)染色。在三个维度上实现了对衣壳热运动的操控。操控过程包括将衣壳嵌入琼脂糖凝胶中。数据表明,凝胶的筛分作用降低了衣壳的热运动。热运动可以降低到任何所需水平。有效扩散常数作为凝胶浓度函数的半对数图是线性的。在存在通过凝胶包埋拉伸并固定的单个DNA分子的情况下,也观察到了单个扩散的T7衣壳。DNA分子用溴化乙锭(橙色荧光)染色。这项研究表明,对于噬菌体衣壳中DNA的包装以及DNA代谢的其他事件,单分子(蛋白质和DNA)分析是可行的。主要问题是生化活性的维持。