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阳离子鸟嘌呤N7 8,9-二氢-8-(N7-鸟嘌呤基)-9-羟基黄曲霉毒素B1加合物5'端的摆动dC.dA配对:对非靶向AFB1诱变的影响。

Wobble dC.dA pairing 5' to the cationic guanine N7 8,9-dihydro-8-(N7-guanyl)-9-hydroxyaflatoxin B1 adduct: implications for nontargeted AFB1 mutagenesis.

作者信息

Giri Indrajit, Stone Michael P

机构信息

Department of Chemistry, Center in Molecular Toxicology, and the Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37235, USA.

出版信息

Biochemistry. 2003 Jun 17;42(23):7023-34. doi: 10.1021/bi020688n.

Abstract

The structure of 5'-d(ACATC(AFB)GATCT)-3'.5'-d(AGATCAATGT)-3', containing the C(5).A(16) mismatch at the base pair 5' to the modified (AFB)G(6), was determined by NMR. The characteristic 5'-intercalation of the AFB(1) moiety was maintained. The mismatched C(5).A(16) pair existed in the wobble conformation, with the C(5) imino nitrogen hydrogen bonded to the A(16) exocyclic amino group. The wobble pair existed as a mixture of protonated and nonprotonated species. The pK(a) for protonation at the A(16) imino nitrogen was similar to that of the C(5).A(16) wobble pair in the corresponding duplex not adducted with AFB(1). Overall, the presence of AFB(1) did not interfere with wobble pair formation at the mismatched site. Molecular dynamics calculations restrained by distances derived from NOE data and torsion angles derived from (1)H (3)J couplings were carried out for both the protonated and nonprotonated wobble pairs at C(5).A(16). Both sets of calculations predicted the A(16) amino group was within 3 A of the C(5) imino nitrogen. The calculations suggested that protonation of the C(5).A(16) wobble pair should shift C(5) toward the major groove and shift A(16) toward the minor groove. The NMR data showed evidence for the presence of a minor conformation characterized by unusual NOEs between T(4) and (AFB)G(6). T(4) is two nucleotides in the 5'-direction from the modified base. These NOEs suggested that in the minor conformation nucleotide T(4) was in closer proximity to (AFB)G(6) than would be expected for duplex DNA. Modeling studies examined the possibility that T(4) transiently paired with the mismatched A(16), allowing it to come within NOE distance of (AFB)G(6). This model structure was consistent with the unusual NOEs associated with the minor conformation. The structural studies are discussed in relationship to nontargeted C --> T transitions observed 5' to the modified (AFB)G in site-specific mutagenesis experiments [Bailey, E. A., Iyer, R. S., Stone, M. P., Harris, T. M., and Essigmann, J. M. (1996) Proc. Natl. Acad. Sci. U.S.A. 93, 1535-1539].

摘要

通过核磁共振(NMR)确定了5'-d(ACATC(AFB)GATCT)-3'.5'-d(AGATCAATGT)-3'的结构,该结构在修饰的(AFB)G(6)上游碱基对处含有C(5).A(16)错配。AFB(1)部分保持了其特征性的5'-嵌入。错配的C(5).A(16)碱基对以摆动构象存在,C(5)亚氨基氮与A(16)环外氨基形成氢键。摆动碱基对以质子化和非质子化形式的混合物存在。A(16)亚氨基氮质子化的pK(a)与相应未与AFB(1)结合的双链体中C(5).A(16)摆动碱基对的pK(a)相似。总体而言,AFB(1)的存在不干扰错配位点处摆动碱基对的形成。对C(5).A(16)处质子化和非质子化摆动碱基对进行了分子动力学计算,计算受源于NOE数据的距离和源于(1)H (3)J耦合的扭转角的限制。两组计算均预测A(16)氨基在C(5)亚氨基氮的3埃范围内。计算表明,C(5).A(16)摆动碱基对的质子化应使C(5)向大沟移动,使A(16)向小沟移动。NMR数据显示存在一种次要构象的证据,其特征是T(4)与(AFB)G(6)之间存在异常的NOE。T(4)在修饰碱基的5'方向上相隔两个核苷酸。这些NOE表明,在次要构象中,核苷酸T(4)与(AFB)G(6)的距离比双链DNA预期的更近。建模研究考察了T(4)与错配的A(16)瞬时配对的可能性,使其能够进入与(AFB)G(6)的NOE距离范围内。该模型结构与次要构象相关的异常NOE一致。结合位点特异性诱变实验[Bailey, E. A., Iyer, R. S., Stone, M. P., Harris, T. M., and Essigmann, J. M. (1996) Proc. Natl. Acad. Sci. U.S.A. 93, 1535 - 1539]中在修饰的(AFB)G上游5'处观察到的非靶向C→T转变,对这些结构研究进行了讨论。

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