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γ-羟基-1,N2-丙烷-2'-脱氧鸟苷 DNA 加合物通过碳醇胺键与 KWKK 肽的 N 末端胺结合。

γ-Hydroxy-1,N2-propano-2'-deoxyguanosine DNA adduct conjugates the N-terminal amine of the KWKK peptide via a carbinolamine linkage.

机构信息

Department of Chemistry, Center in Molecular Toxicology, Center for Structural Biology, Vanderbilt University, Nashville, Tennessee 37235, USA.

出版信息

Chem Res Toxicol. 2011 Jul 18;24(7):1123-33. doi: 10.1021/tx200113n. Epub 2011 May 11.

Abstract

The γ-hydroxy-1,N(2)-propano-2'-deoxyguanosine adduct (γ-OH-PdG) was introduced into 5'-d(GCTAGCXAGTCC)-3'·5'-d(GGACTCGCTAGC)-3' (X = γ-OH-PdG). In the presence of excess peptide KWKK, (13)C isotope-edited NMR revealed the formation of two spectroscopically distinct DNA-KWKK conjugates. These involved the reaction of the KWKK N-terminal amino group with the N(2)-dG propylaldehyde tautomer of the γ-OH-PdG lesion. The guanine N1 base imino resonance at the site of conjugation was observed in isotope-edited (15)N NMR experiments, suggesting that the conjugated guanine was inserted into the duplex and that the guanine imino proton was protected from exchange with water. The conjugates could be reduced in the presence of NaCNBH(3), suggesting that they existed, in part, as imine (Schiff base) linkages. However, (13)C isotope-edited NMR failed to detect the imine linkages, suggesting that these KWKK conjugates existed predominantly as diastereomeric carbinolamines, in equilibrium with trace amounts of the imines. The structures of the diastereomeric DNA-KWKK conjugates were predicted from potential energy minimization of model structures derived from the refined structure of the fully reduced cross-link [ Huang, H., Kozekov, I. D., Kozekova, A., Rizzo, C. J., McCullough, A., Lloyd, R. S., and Stone, M. P. ( 2010 ) Biochemistry , 49 , 6155 -6164 ]. Molecular dynamics calculations carried out in explicit solvent suggested that the conjugate bearing the S-carbinolamine linkage was the major species due to its potential for intramolecular hydrogen bonding. These carbinolamine DNA-KWKK conjugates thermally stabilized duplex DNA. However, the DNA-KWKK conjugates were chemically reversible and dissociated when the DNA was denatured. In this 5'-CpX-3' sequence, the DNA-KWKK conjugates slowly converted to interstrand N(2)-dG:N(2)-dG DNA cross-links and ring-opened γ-OH-PdG derivatives over a period of weeks.

摘要

γ-羟基-1,N(2)-丙烷-2'-脱氧鸟苷加合物(γ-OH-PdG)被引入到 5'-d(GCTAGCXAGTCC)-3'·5'-d(GGACTCGCTAGC)-3'(X = γ-OH-PdG)中。在过量肽 KWKK 的存在下,(13)C 同位素编辑 NMR 揭示了两种光谱上明显不同的 DNA-KWKK 缀合物的形成。这些涉及 KWKK N-末端氨基与 γ-OH-PdG 损伤的 N(2)-dG 丙醛互变异构体的反应。在同位素编辑(15)N NMR 实验中观察到偶联部位的鸟嘌呤 N1 碱基亚氨基共振,表明共轭鸟嘌呤插入双链体中,并且鸟嘌呤亚氨基质子受到保护免受与水的交换。在 NaCNBH(3)的存在下,这些缀合物可以被还原,这表明它们部分存在于亚胺(席夫碱)键中。然而,(13)C 同位素编辑 NMR 未能检测到亚胺键,表明这些 KWKK 缀合物主要以非对映醇胺的形式存在,与痕量亚胺处于平衡状态。通过从完全还原的交联的精细结构得出的模型结构的势能最小化预测了非对映醇胺 DNA-KWKK 缀合物的结构[Huang,H.,Kozekov,I.D.,Kozekova,A.,Rizzo,C.J.,McCullough,A.,Lloyd,R.S.,and Stone,M.P.(2010)Biochemistry,49,6155-6164]。在明确溶剂中进行的分子动力学计算表明,由于其具有形成分子内氢键的潜力,带有 S-醇胺键的缀合物是主要物种。这些醇胺 DNA-KWKK 缀合物热稳定双链 DNA。然而,当 DNA 变性时,DNA-KWKK 缀合物是化学可逆的并且解离。在这个 5'-CpX-3'序列中,DNA-KWKK 缀合物在数周内缓慢转化为链间 N(2)-dG:N(2)-dG DNA 交联和开环的 γ-OH-PdG 衍生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f670/3138414/e326c963a55a/tx-2011-00113n_0007.jpg

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