Shukla S K, McCarthy D
Department of Botany and Microbiology, University of Oklahoma, Norman 73019-0245.
Nucleic Acids Res. 1994 May 11;22(9):1626-31. doi: 10.1093/nar/22.9.1626.
An activity gel assay was developed for the detection of DNA helicases in crude extracts. The assay was based on the ability of DNA helicases to unwind radioactive fragments from single-stranded M13 circles that were immobilized in an SDS polyacrylamide gel. The displaced radioactive strands were detected by blotting them to a filter and visualizing the resulting bands by autoradiography. Experiments with purified proteins demonstrated that DNA helicases, endonucleases and exonucleases could produce activity bands. A one-dimensional gel assay was sufficiently sensitive to allow detection of DNA helicase I, DNA helicase II, DNA helicase IV, the RecQ helicase as well as 3 unidentified putative DNA helicases in crude extracts of Escherichia coli. Exonuclease and endonuclease activities from crude extracts could be distinguished from DNA helicase activities by their ATP-independence and from each other by their band morphologies.
开发了一种活性凝胶测定法,用于检测粗提物中的DNA解旋酶。该测定法基于DNA解旋酶从固定在SDS聚丙烯酰胺凝胶中的单链M13环解开放射性片段的能力。通过将置换出的放射性链印迹到滤膜上并通过放射自显影观察所得条带,来检测这些链。对纯化蛋白质的实验表明,DNA解旋酶、核酸内切酶和核酸外切酶均可产生活性条带。一维凝胶测定法灵敏度足够高,能够检测大肠杆菌粗提物中的DNA解旋酶I、DNA解旋酶II、DNA解旋酶IV、RecQ解旋酶以及3种未鉴定的假定DNA解旋酶。粗提物中的核酸外切酶和核酸内切酶活性可因其不依赖ATP而与DNA解旋酶活性区分开来,且可通过其条带形态相互区分。