Oh E Y, Grossman L
Department of Biochemistry, Johns Hopkins University School of Hygiene and Public Health, Baltimore, Maryland 21205.
J Biol Chem. 1989 Jan 15;264(2):1336-43.
The requirement for nucleotide hydrolysis in the DNA repair mechanism of the Escherichia coli UvrABC protein complex has been analyzed. The DNA-activated UvrAB ATPase activity is part of a helicase activity exhibited by the UvrAB protein complex. The helicase acts only on short duplexes and, therefore, is unlike other helicases such as those involved in DNA replication that unwind long duplexes. The strand displacement activity occurs in the 5'----3' direction and requires either ATP or dATP. The helicase activity is inhibited by UV photoproducts. The absence of this activity in a complex formed with proteolyzed UvrB (UvrB*), a complex also deficient in the endonuclease activity, suggests that this activity is important in the repair mechanism. The UvrAB protein complex may remain bound to a damaged site and by coupling the energy derived from ATP hydrolysis, alter the DNA conformation around the damage site to one that is permissive for endonucleolytic events. The conformational changes may take the form of DNA unwinding.
对大肠杆菌UvrABC蛋白复合物DNA修复机制中核苷酸水解的要求进行了分析。DNA激活的UvrAB ATP酶活性是UvrAB蛋白复合物展现的解旋酶活性的一部分。该解旋酶仅作用于短双链体,因此不同于其他解旋酶,如参与DNA复制、解开长双链体的那些解旋酶。链置换活性沿5'→3'方向发生,需要ATP或dATP。解旋酶活性受紫外线光产物抑制。在与经蛋白酶水解的UvrB(UvrB*)形成的复合物中缺乏这种活性,该复合物也缺乏内切核酸酶活性,这表明这种活性在修复机制中很重要。UvrAB蛋白复合物可能仍与损伤位点结合,并通过耦合ATP水解产生的能量,将损伤位点周围的DNA构象改变为有利于内切核酸酶作用的构象。构象变化可能表现为DNA解旋的形式。