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Mapping the nicking efficiencies of nickase R.BbvCI for side-specific LNA-substituted substrates using rolling circle amplification

机译:使用滚环扩增法绘制切口酶R.BbvCI对侧特异性LNA取代的底物的切刻效率

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We used a novel asymmetric cleavage analysis method based on rolling circle amplification (RCA) to determine the effects of LNA modification of substrate on the two subunits of R.BbvCI cleavage. We designed two sets of cleavage circular substrates by using two different ligation strategies and analyzed the single strand cleavage efficiency affected by different modification positions both from the cleaved strands and the uncleaved strands. Results showed that the effects of LNA on cleavage rates of modified strands and unmodified strands were both site-dependent. The Nb.BbvCI and Nt.BbvCI were affected by LNA modification in different way. Most of the modification positions showed strong inhibition of both of these two nickases cleavage. However, the modification in T3 position of bottom strand hardly affected both of the two nickases activities. The results suggested an intimated interaction between the two subunits of R.BbvCI, and the T3 position in bottom strand might be a less tight position which was hard to be disturbed.
机译:我们使用基于滚环扩增(RCA)的新型不对称裂解分析方法来确定底物的LNA修饰对R.BbvCI裂解的两个亚基的影响。我们使用两种不同的连接策略设计了两组裂解圆形底物,并分析了裂解链和未裂解链受不同修饰位置影响的单链裂解效率。结果表明,LNA对修饰链和未修饰链的切割速率的影响均是位点依赖性的。 Nb.BbvCI和Nt.BbvCI受LNA修饰的方式不同。大多数修饰位点都显示出对这两种切口酶切割均具有强烈的抑制作用。然而,底部链的T3位置的修饰几乎不影响两个切口酶的活性。结果表明,R.BbvCI的两个亚基之间存在紧密的相互作用,底部链中的T3位置可能不太紧,很难被干扰。

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