Hansma H G, Golan R, Hsieh W, Daubendiek S L, Kool E T
Department of Physics, University of California, Santa Barbara, Santa Barbara, California 93106-9530, USA.
J Struct Biol. 1999 Oct;127(3):240-7. doi: 10.1006/jsbi.1999.4170.
The structures of the reaction products are the basis for novel polymerase assays using the atomic force microscope (AFM). Polymerases are the enzymes involved in transcription and replication of DNA. Rapid semiquantitative estimates of the activity of DNA polymerases such as Sequenase, Taq polymerase, and AMV reverse transcriptase and RNA polymerases (RNAP) such as Escherichia coli RNAP were obtained from AFM images of the nucleic acids after polymerase reactions. DNA polymerases were assayed via replication of the single-stranded φX-174 virion. RNAP was assayed via transcription, using a rolling circle DNA template that produces long strands of RNA. In some cases, AFM was better than agarose gel electrophoresis for assaying DNA polymerase activity, since aggregation prevented the DNA from entering the agarose gel. Extended molecules of single-stranded RNA synthesized with the rolling circle DNA template showed varied conformations and degrees of stretching. Some structural differences were observed between two RNAs-a ribozyme concatamer and an RNA with 90% purines.
反应产物的结构是使用原子力显微镜(AFM)进行新型聚合酶测定的基础。聚合酶是参与DNA转录和复制的酶。通过聚合酶反应后核酸的AFM图像,可以快速半定量估计诸如测序酶、Taq聚合酶和AMV逆转录酶等DNA聚合酶以及诸如大肠杆菌RNA聚合酶(RNAP)等RNA聚合酶的活性。通过单链φX-174病毒粒子的复制来测定DNA聚合酶。使用产生长链RNA的滚环DNA模板通过转录来测定RNAP。在某些情况下,AFM在测定DNA聚合酶活性方面优于琼脂糖凝胶电泳,因为聚集会阻止DNA进入琼脂糖凝胶。用滚环DNA模板合成的单链RNA延伸分子显示出不同的构象和伸展程度。在两种RNA之间观察到一些结构差异——一种核酶串联体和一种嘌呤含量为90%的RNA。