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DNA聚合酶III全酶的β亚基在与引发DNA形成起始复合物后,抗体无法再与之结合。

The beta subunit of the DNA polymerase III holoenzyme becomes inaccessible to antibody after formation of an initiation complex with primed DNA.

作者信息

Johanson K O, McHenry C S

出版信息

J Biol Chem. 1982 Oct 25;257(20):12310-5.

PMID:7118945
Abstract

The initiation of the DNA polymerase III holoenzyme-catalyzed reaction is blocked by antibody directed against the beta subunit; elongation is unaffected (Johanson, K., and McHenry, C. (1980) J. Biol. Chem. 255, 10984-10990). We have developed an immunological method for quantitating nanogram quantities of beta in reaction complexes. Using this method, we have demonstrated that beta is present in all stages of the DNA polymerase III holoenzyme reaction. Upon initiation complex formation, the antigenic determinants of beta become inaccessible to anti-beta immunoglobulin G. The methods described herein should be generally applicable to the study of a variety of multienzyme complexes. Even after conversion of a primed G4 single strand to the duplex replicative form, beta does not readily dissociate. This creates a kinetic barrier to the overall holoenzyme replicative reaction.

摘要

针对β亚基的抗体可阻断DNA聚合酶III全酶催化反应的起始;延伸不受影响(约翰森,K.,和麦克亨利,C.(1980年)《生物化学杂志》255卷,10984 - 10990页)。我们开发了一种免疫方法来定量反应复合物中纳克量的β亚基。使用这种方法,我们证明了β亚基存在于DNA聚合酶III全酶反应的所有阶段。在起始复合物形成时,β亚基的抗原决定簇对于抗β免疫球蛋白G变得不可接近。本文所述方法应普遍适用于各种多酶复合物的研究。即使在将引发的G4单链转化为双链复制形式后,β亚基也不容易解离。这为全酶的整体复制反应创造了动力学障碍。

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