Jenkins T C, Hurley L H, Neidle S, Thurston D E
Cancer Research Campaign Biomolecular Structure Unit, Institute of Cancer Research, Sutton, Surrey, U.K.
J Med Chem. 1994 Dec 23;37(26):4529-37. doi: 10.1021/jm00052a012.
The structure of the interstrand cross-linked adduct formed between a C8-C8'-linked pyrrolobenzodiazepine (PBD) dimer (DSB-120; 1,1'-(propane-1,3-diyldioxy)bis[(11aS)-7-methoxy-1,2,3,11a-t etrahydro-5H- pyrrolo[2,1-c][1,4]benzodiazepin-5-one]) and a self-complementary d(CICGATCICG)2 duplex has been determined from high-field 1D- and 2D-NMR data using a simulated annealing procedure. The refined structure supports earlier observations from solution NMR experiments and indicates that the covalently bound molecule spans six DNA base pairs in the minor groove, forming a symmetric cross-link between the spatially separated internal guanines and with active recognition of an embedded 5'-GATC bonding site. This result confirms that template-directed approaches are useful for the design of linked DNA-interactive PBD dimers with viable DNA cross-linking potential. Further, head-to-head connection of the PBD moieties results in an overall retention of 5'-GA bonding site preference for each alkylating PBD subunit. Structural analysis indicates that cross-link formation results in a localized perturbation of the DNA duplex, attributable in part to a mutual reduction in dynamic mobility or "covalent clamping" within the Gua4-Cyt7 base tract. However, ligand-induced distortion is confined to the Cyt7 and Ino8 residues on each strand. The Gua(N2)-Gua(N2) cross-link is stabilized by two directed H-bonds from the formed animal residues to N3 acceptor atoms of adenine bases on the 3'-side of each covalently modified guanine. Evidence for sequence-specific cross-linking with DSB-120 is provided by extended modeling studies which suggest that recognition of the favored d(.GATC.) motif is dominated by van der Waals steric factors, although electrostatic and H-bonded interaction terms also play a key role. This conclusion supports recent covalent footprinting studies revealing that this PBD dimer shows a selectivity for embedded base sequences of the type 5'-(pu/py)GATC(py/pu).
通过模拟退火程序,利用高场一维和二维核磁共振数据,确定了在C8 - C8'连接的吡咯并苯并二氮杂卓(PBD)二聚体(DSB - 120;1,1'-(丙烷 - 1,3 - 二氧)双[(11aS)- 7 - 甲氧基 - 1,2,3,11a - 四氢 - 5H - 吡咯并[2,1 - c][1,4]苯并二氮杂卓 - 5 - 酮])与自互补d(CICGATCICG)2双链体之间形成的链间交联加合物的结构。优化后的结构支持了溶液核磁共振实验的早期观察结果,表明共价结合的分子在小沟中跨越六个DNA碱基对,在空间上分离的内部鸟嘌呤之间形成对称交联,并对嵌入的5'-GATC结合位点有活性识别。这一结果证实了模板导向方法对于设计具有可行DNA交联潜力的连接DNA相互作用PBD二聚体是有用的。此外,PBD部分的头对头连接导致每个烷基化PBD亚基对5'-GA结合位点偏好的总体保留。结构分析表明,交联形成导致DNA双链体的局部扰动,部分归因于Gua4 - Cyt7碱基序列内动态流动性的相互降低或“共价钳制”。然而,配体诱导的扭曲仅限于每条链上的Cyt7和Ino8残基。Gua(N2)- Gua(N2)交联通过来自形成的氨基残基到每个共价修饰鸟嘌呤3'侧腺嘌呤碱基的N3受体原子的两个定向氢键得以稳定。扩展的建模研究提供了与DSB - 120序列特异性交联的证据,这些研究表明,对有利的d(.GATC.)基序的识别主要由范德华空间因素主导,尽管静电和氢键相互作用项也起着关键作用。这一结论支持了最近的共价足迹研究,该研究表明这种PBD二聚体对5' - (嘌呤/嘧啶)GATC(嘧啶/嘌呤)类型的嵌入碱基序列具有选择性。