Orbons L P, van Beuzekom A A, Altona C
Gorlaeus Laboratories, Leiden University, The Netherlands.
J Biomol Struct Dyn. 1987 Jun;4(6):965-87. doi: 10.1080/07391102.1987.10507692.
The hairpin form of the mismatched octamer d(m5C-G-m5C-G-T-G-m5C-G) was studied by means of NMR spectroscopy. In a companion study it is shown that the hairpin form of this DNA fragment consists of a structure with a stem of three Watson-Crick-type base pairs and a loop consisting of only two nucleotides. The non-exchangeable proton resonances were assigned by means of two-dimensional correlation spectroscopy and two-dimensional nuclear Overhauser effect spectroscopy. Proton-proton coupling constants were used for the conformational analysis of the deoxyribose ring and for some of the backbone torsion angles. From the two-dimensional NMR spectra and the coupling-constant analysis it is concluded that: (i) the stem of the hairpin exhibits B-DNA characteristics; (ii) the sugar rings are not conformationally pure, but display a certain amount of conformational flexibility; (iii) the stacking interaction in the stem of the hairpin is elongated from the 3'-side in a more or less regular fashion with the two loop nucleotides; (iv) at the 5'-side of the stem a stacking discontinuity occurs between the stem and the loop; (v) at the 5'-side of the stem the loop is closed by means of a sharp backbone turn which involves unusual gamma' and beta+ torsion angles in residue dG(6). The NMR results led to the construction of a hairpin-loop model which was energy-minimized by means of a molecular-mechanics program. The results clearly show that a DNA hairpin-loop structure in which the loop consists of only two nucleotides bridging the minor groove in a straightforward fashion, (i) causes no undue steric strain, and (ii) involves well-known conformational principles throughout the course of the backbone. The hairpin form of the title compound is compared with the hairpin form of d(A-T-C-C-T-A-T4-T-A-G-G-A-T), in which the central -T4- part forms a loop of four nucleotides. Both models display similarities as far as stacking interactions are concerned.
通过核磁共振光谱法研究了错配八聚体d(m5C-G-m5C-G-T-G-m5C-G)的发夹形式。在一项相关研究中表明,该DNA片段的发夹形式由一个具有三个沃森-克里克型碱基对的茎和一个仅由两个核苷酸组成的环的结构组成。通过二维相关光谱法和二维核Overhauser效应光谱法确定了不可交换质子共振。质子-质子耦合常数用于脱氧核糖环的构象分析和一些主链扭转角的分析。从二维核磁共振光谱和耦合常数分析得出以下结论:(i)发夹的茎表现出B-DNA特征;(ii)糖环的构象不纯,但表现出一定程度的构象灵活性;(iii)发夹茎中的堆积相互作用从3'侧以或多或少规则的方式与两个环核苷酸拉长;(iv)在茎的5'侧,茎和环之间出现堆积不连续;(v)在茎的5'侧,环通过一个尖锐的主链转折闭合,该转折涉及dG(6)残基中不寻常的γ'和β+扭转角。核磁共振结果导致构建了一个发夹环模型,该模型通过分子力学程序进行了能量最小化。结果清楚地表明,一种DNA发夹环结构,其中环仅由两个以直接方式跨越小沟的核苷酸组成,(i)不会引起过度的空间应变,并且(ii)在整个主链过程中涉及众所周知的构象原理。将标题化合物的发夹形式与d(A-T-C-C-T-A-T4-T-A-G-G-A-T)的发夹形式进行了比较,其中中央-T4-部分形成了一个由四个核苷酸组成的环。就堆积相互作用而言,两个模型都显示出相似性。