Loeber Rachel, Michaelson Erin, Fang Qingming, Campbell Colin, Pegg Anthony E, Tretyakova Natalia
Department of Medicinal Chemistry and Cancer Center and Department of Pharmacology, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Chem Res Toxicol. 2008 Apr;21(4):787-95. doi: 10.1021/tx7004508. Epub 2008 Feb 14.
The antitumor activity of chemotherapeutic nitrogen mustards including chlorambucil, cyclophosphamide, and melphalan is commonly attributed to their ability to induce DNA-DNA cross-links by consecutive alkylation of two nucleophilic sites within the DNA duplex. DNA-protein cross-linking by nitrogen mustards is not well characterized, probably because of its inherent complexity and the insufficient sensitivity of previous methodologies. If formed, DNA-protein conjugates are likely to contribute to both target and off-target cytotoxicity of nitrogen mustard drugs. Here, we show that the DNA repair protein, O (6)-alkylguanine DNA alkyltransferase (AGT), can be readily cross-linked to DNA in the presence of nitrogen mustards. Both chlorambucil and mechlorethamine induced the formation of covalent conjugates between (32)P-labeled double-stranded oligodeoxynucleotides and recombinant human AGT protein, which were detected by SDS-PAGE. Capillary HPLC-electrospray ionization mass spectrometry (ESI-MS) analysis of AGT that had been treated with the guanine half-mustards of chlorambucil or mechlorethamine revealed the ability of the protein to form either one or two cross-links to guanine. C145A AGT (a variant containing a single point mutation in the protein's active site) was found capable of forming a single guanine conjugate, while cross-linking was virtually abolished upon treatment of the C145A/C150S AGT double mutant with the guanine half-mustards. HPLC-ESI (+)-MS/MS sequencing of tryptic peptides obtained from the wild-type AGT protein that had been treated with nitrogen mustards in the presence of DNA confirmed that the cross-linking took place between the N7 position of guanine in DNA and two active site residues within the AGT protein (Cys (145) and Cys (150)). The exact chemical structures of AGT-DNA cross-links induced by chlorambucil and mechlorethamine were identified as N-(2-[ S-cysteinyl]ethyl)- N-(2-[guan-7-yl]ethyl)- p-aminophenylbuyric acid and N-(2-[ S-cysteinyl]ethyl)- N-(2-[guan-7-yl]ethyl)methylamine, respectively, based upon HPLC-MS/MS analysis of protein hydrolysates in parallel with the corresponding amino acid conjugates prepared synthetically. Mechlorethamine-induced AGT-DNA conjugates were isolated from protein extracts of AGT-expressing CHO cells but not control cells, demonstrating that nitrogen mustards can cross-link the AGT protein to DNA in the presence of other nuclear proteins. Because AGT is overexpressed in many tumor types, further investigations of the potential role of AGT-DNA cross-linking in the antitumor and mutagenic activity of antitumor nitrogen mustards are warranted.
包括苯丁酸氮芥、环磷酰胺和美法仑在内的化疗性氮芥的抗肿瘤活性通常归因于它们通过对DNA双链体内两个亲核位点进行连续烷基化来诱导DNA-DNA交联的能力。氮芥引起的DNA-蛋白质交联尚未得到充分表征,这可能是由于其内在的复杂性以及先前方法的灵敏度不足。如果形成,DNA-蛋白质共轭物可能会导致氮芥药物的靶向和脱靶细胞毒性。在此,我们表明,在氮芥存在的情况下,DNA修复蛋白O(6)-烷基鸟嘌呤DNA烷基转移酶(AGT)可以很容易地与DNA交联。苯丁酸氮芥和氮芥均诱导(32)P标记的双链寡脱氧核苷酸与重组人AGT蛋白之间形成共价共轭物,通过SDS-PAGE检测到。对用苯丁酸氮芥或氮芥的鸟嘌呤半氮芥处理过的AGT进行毛细管HPLC-电喷雾电离质谱(ESI-MS)分析,结果显示该蛋白能够与鸟嘌呤形成一个或两个交联。发现C145A AGT(一种在蛋白活性位点含有单点突变的变体)能够形成单个鸟嘌呤共轭物,而在用鸟嘌呤半氮芥处理C145A/C150S AGT双突变体后,交联实际上被消除。对在DNA存在下用氮芥处理过的野生型AGT蛋白获得的胰蛋白酶肽段进行HPLC-ESI(+)-MS/MS测序,证实交联发生在DNA中鸟嘌呤的N7位置与AGT蛋白内的两个活性位点残基(半胱氨酸(145)和半胱氨酸(150))之间。基于对蛋白质水解产物与合成制备的相应氨基酸共轭物的平行HPLC-MS/MS分析,由苯丁酸氮芥和氮芥诱导的AGT-DNA交联的确切化学结构分别被鉴定为N-(2-[S-半胱氨酰基]乙基)-N-(2-[鸟嘌呤-7-基]乙基)-对氨基苯基丁酸和N-(2-[S-半胱氨酰基]乙基)-N-(2-[鸟嘌呤-7-基]乙基)甲胺。从表达AGT的CHO细胞而非对照细胞的蛋白质提取物中分离出氮芥诱导的AGT-DNA共轭物,这表明在存在其他核蛋白的情况下,氮芥可以使AGT蛋白与DNA交联。由于AGT在许多肿瘤类型中过表达,因此有必要进一步研究AGT-DNA交联在抗肿瘤氮芥的抗肿瘤和诱变活性中的潜在作用。