Joubert Allison M, Byrd Angela S, LiCata Vince J
Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803, USA.
J Biol Chem. 2003 Jul 11;278(28):25341-7. doi: 10.1074/jbc.M302118200. Epub 2003 May 3.
Escherichia coli polymerase 1 (Pol 1) and Thermus aquaticus Taq polymerase are homologous Type I DNA polymerases, each comprised of a polymerase domain, a proofreading domain (inactive in Taq), and a 5' nuclease domain. "Klenow" and "Klentaq" are the large fragments of Pol 1 and Taq and are functional polymerases lacking the 5' nuclease domain. In the available crystal structures of full-length Taq, the 5' nuclease domain is positioned in two different orientations: in one structure, it is extended out into solution, whereas in the other, it is folded up against the polymerase domain in a more compact structure. Analytical ultracentrifugation experiments report s20,w values of 5.05 for Taq, 4.1 for Klentaq, 5.3 for E. coli Pol 1, and 4.6 for Klenow. Measured partial specific volumes are all quite similar, indicating no significant differences in packing density between the mesophilic and thermophilic proteins. Small angle x-ray scattering studies report radii of gyration of 38.3 A for Taq, 30.7 A for Klentaq, and 30.5 A for Klenow. The hydrodynamic and x-ray scattering properties of the polymerases were also calculated directly from the different crystal structures using the programs HYDROPRO (Garcia De La Torre, J., Huertas, M. L., and Carrasco, B. (2000) Biophys J. 78, 719-730) and CRYSOL (Svergun, D. I., Barberato, C., and Koch, M. H. J. (1995) J. Appl. Crystalogr. 28, 768-773), respectively. The combined experimental and computational characterizations indicate that the full-length polymerases in solution are in a conformation where the 5' nuclease domain is extended into solution. Further, the radius of gyration, and hence the global conformation of Taq polymerase, is not altered by the binding of either matched primer template DNA or ddATP.
大肠杆菌聚合酶1(Pol 1)和嗜热水生栖热菌Taq聚合酶是同源的I型DNA聚合酶,每种都由一个聚合酶结构域、一个校对结构域(在Taq中无活性)和一个5'核酸酶结构域组成。“Klenow”和“Klentaq”分别是Pol 1和Taq的大片段,是缺少5'核酸酶结构域的功能性聚合酶。在全长Taq的现有晶体结构中,5'核酸酶结构域以两种不同的方向定位:在一种结构中,它延伸到溶液中,而在另一种结构中,它以更紧凑的结构折叠在聚合酶结构域上。分析超速离心实验报告Taq的s20,w值为5.05,Klentaq为4.1,大肠杆菌Pol 1为5.3,Klenow为4.6。测得的部分比容都非常相似,表明嗜温蛋白和嗜热蛋白之间的堆积密度没有显著差异。小角x射线散射研究报告Taq的回转半径为38.3 Å,Klentaq为30.7 Å,Klenow为30.5 Å。还分别使用HYDROPRO程序(Garcia De La Torre, J., Huertas, M. L., and Carrasco, B. (2000) Biophys J. 78, 719 - 730)和CRYSOL程序(Svergun, D. I., Barberato, C., and Koch, M. H. J. (1995) J. Appl. Crystalogr. 28, 768 - 773)直接从不同的晶体结构计算聚合酶的流体动力学和x射线散射特性。综合实验和计算表征表明,溶液中的全长聚合酶处于5'核酸酶结构域延伸到溶液中的构象。此外,Taq聚合酶的回转半径以及整体构象不会因匹配的引物模板DNA或ddATP的结合而改变。