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蛋白质诱导DNA弯曲的两种不同模式。

Two distinct modes of protein-induced bending in DNA.

作者信息

El Hassan M A, Calladine C R

机构信息

Department of Engineering, University of Cambridge, Cambridge, CB2 1PZ, UK.

出版信息

J Mol Biol. 1998 Sep 18;282(2):331-43. doi: 10.1006/jmbi.1998.1994.

Abstract

Crystallised "naked" DNA oligomers in the B form show significant conformational mobility, particularly at CA/TG and TA/TA steps: there is a range in Roll angle of some 15 degrees between consecutive base-pairs, and Slide and Twist are directly coupled to Roll. We call such motions "mode I". They are sufficient to enable DNA to curve gently around proteins such as histone octamers in the nucleosome particle. When DNA bends around other proteins, such as CAP and TBP, its distortion is much more severe. Although the DNA in close contact with these proteins includes the CA/TG and TA/TA steps, respectively, the mode I flexibility is not deployed: instead, a more severe "mode II" manoeuvre is observed in DNA/protein co-crystals. Mode II has several distinctive physical features. First, its range of Roll angle is much wider than for mode I. Second, the major-groove width remains more-or-less constant as Roll increases, whereas it decreases significantly as Roll increases in mode I; and this enables the major groove of the DNA to accommodate a protein moiety in its severely bent conformation. Third, the value of Slide remains more-or-less constant as Roll increases, whereas it decreases in mode I. In general, in both modes I and II, the major-groove width appears to be closely related to the Slide between base-pairs. In mode II there appears to be a definite "point pivot" on the major-groove side of the two base-pairs that constitute a dinucleotide step, formed either by the steric interlocking of propeller-twisted base-pairs or by a bifurcated hydrogen bond. Distortion of DNA in mode II seems to be an intrinsic property of the double-helical structure, since it occurs whether protein is bound on the major-groove side (e.g. CAP) or on the minor-groove side (e.g. TBP). Mode II distortion occurs in a wider range of steps than those that show the largest mode-I variation; nevertheless, "access" to mode II deformation appears to be gained via mode I distortion at particular steps CA/TG and TA/TA.

摘要

呈B型的结晶“裸露”DNA寡聚物表现出显著的构象灵活性,尤其是在CA/TG和TA/TA步:连续碱基对之间的滚动角范围约为15度,滑动和扭转与滚动直接相关。我们将这种运动称为“模式I”。它们足以使DNA围绕核小体颗粒中的组蛋白八聚体等蛋白质轻轻弯曲。当DNA围绕其他蛋白质(如CAP和TBP)弯曲时,其扭曲要严重得多。尽管与这些蛋白质紧密接触的DNA分别包含CA/TG和TA/TA步,但模式I的灵活性并未发挥作用:相反,在DNA/蛋白质共晶体中观察到更严重的“模式II”操作。模式II有几个独特的物理特征。首先,其滚动角范围比模式I宽得多。其次,随着滚动增加,大沟宽度基本保持不变,而在模式I中随着滚动增加它会显著减小;这使得DNA的大沟能够容纳处于严重弯曲构象的蛋白质部分。第三,随着滚动增加,滑动值基本保持不变,而在模式I中它会减小。一般来说,在模式I和模式II中,大沟宽度似乎与碱基对之间的滑动密切相关。在模式II中,在构成二核苷酸步的两个碱基对的大沟侧似乎有一个明确的“点枢轴”,它由螺旋扭曲碱基对的空间互锁或分叉氢键形成。模式II中DNA的扭曲似乎是双螺旋结构的固有特性,因为无论蛋白质结合在大沟侧(如CAP)还是小沟侧(如TBP)都会发生。模式II扭曲发生的步比显示最大模式I变化的步范围更广;然而,似乎是通过特定步CA/TG和TA/TA处的模式I扭曲来实现模式II变形的“进入”。

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