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博来霉素与羟基自由基诱导DNA中丙二醛产物的形成

Bleomycin versus OH-radical-induced malonaldehydic-product formation in DNA.

作者信息

Rashid R, Langfinger D, Wagner R, Schuchmann H P, von Sonntag C

机构信息

Max-Planck-Institut für Strahlenchemie, Mülheim an der Ruhr, Germany.

出版信息

Int J Radiat Biol. 1999 Jan;75(1):101-9. doi: 10.1080/095530099140852.

Abstract

PURPOSE

To compare the actions of bleomycin and ionizing radiation on DNA regarding the formation of malonaldehyde-like products.

MATERIALS AND METHODS

Calf thymus DNA was treated with iron/bleomycin or gamma-radiation at pH 7. Products were analysed by HPLC. The thiobarbituric-acid reactivity of the samples was determined directly or after HPLC by post-column derivatization. ESI mass spectra were taken on-line following HPLC.

RESULTS

Malonaldehyde and malonaldehyde-like products as detected by the sensitive 2-thiobarbituric acid (TBA) assay are formed in gamma-irradiated DNA and thymidine solutions as well as upon treatment of DNA with bleomycin/iron. In gamma-irradiated DNA solutions in the presence of oxygen, no base propenals were detected, and the major TBA-active product was malonaldehyde. In the gamma-radiolysis of thymidine, thymine propenal was formed only in traces (not more than 0.07 per cent of the OH-radical yield). Malonaldehyde was practically absent after treatment with bleomycin; three other TBA-active products were seen by HPLC which have been identified as the cytosine, thymine, and adenine propenals. Guanine propenal was not detected under our conditions.

CONCLUSIONS

The absence of these base propenals upon gamma-radiolysis implies that although the initiating step of OH-radical and bleomycin action [i.e. H-abstraction at C(4')] may be the same, the bleomycin-iron complex must participate in subsequent steps en route to the base propenals. It is proposed that the bleomycin pathway may involve the interaction of the C(4')-peroxyl radical with the 'spent' bleomycin-iron complex by ligand exchange, under formation of a bleomycin-iron-peroxyl-radical complex, Blm(Fe4+,*OOR), which then decomposes by heterolysis into the alkoxy cation precursor +OR of the base propenal and reconstitution of the bleomycin-iron complex Blm(Fe,O)3+, i.e. gives rise to base propenal formation without the involvement of a C(4')-hydroperoxide.

摘要

目的

比较博来霉素和电离辐射对DNA形成丙二醛样产物的作用。

材料与方法

在pH 7条件下,用铁/博来霉素或γ射线处理小牛胸腺DNA。产物通过高效液相色谱(HPLC)分析。样品的硫代巴比妥酸反应性通过柱后衍生化直接测定或在HPLC后测定。HPLC后在线采集电喷雾电离质谱(ESI)。

结果

通过灵敏的2-硫代巴比妥酸(TBA)测定法检测到,γ射线照射的DNA和胸腺嘧啶溶液中以及用博来霉素/铁处理DNA时会形成丙二醛和丙二醛样产物。在有氧存在的情况下,γ射线照射的DNA溶液中未检测到碱基丙烯醛,主要的TBA活性产物是丙二醛。在胸腺嘧啶的γ射线分解中,胸腺嘧啶丙烯醛仅以痕量形式形成(不超过OH自由基产率的0.07%)。用博来霉素处理后几乎没有丙二醛;HPLC检测到另外三种TBA活性产物,已鉴定为胞嘧啶、胸腺嘧啶和腺嘌呤丙烯醛。在我们的条件下未检测到鸟嘌呤丙烯醛。

结论

γ射线分解时这些碱基丙烯醛的缺失意味着,尽管OH自由基和博来霉素作用的起始步骤[即C(4')处的氢原子提取]可能相同,但博来霉素-铁复合物在形成碱基丙烯醛的后续步骤中必定参与其中。有人提出,博来霉素途径可能涉及C(4')-过氧自由基与“用过的”博来霉素-铁复合物通过配体交换相互作用,形成博来霉素-铁-过氧自由基复合物Blm(Fe4+,*OOR),然后通过异裂分解为碱基丙烯醛的烷氧基阳离子前体+OR,并使博来霉素-铁复合物Blm(Fe,O)3+重构,即导致碱基丙烯醛的形成而不涉及C(4')-氢过氧化物。

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