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首页> 外文期刊>Journal of biochemical and molecular toxicology >Adduct-forming tendencies of cationic triarylmethane dyes with proteins: Metabolic and toxicological implications.
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Adduct-forming tendencies of cationic triarylmethane dyes with proteins: Metabolic and toxicological implications.

机译:阳离子三芳基甲烷染料与蛋白质形成加合物的趋势:代谢和毒理学意义。

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摘要

The formation of colorless adducts by four cationic triarylmethane dyes (TAM(+)s), methyl green (MeG(+)), malachite green (MG(+)), pararosaniline (PR(+)), and crystal violet (CV(+)) was studied spectrophotometrically at 25 degrees C, in 50 mM 3-(N-morpholino)propanesulfonic acid (MOPS) buffer (pH 8), by monitoring the loss in TAM(+) color in the absence and presence of human serum proteins as potential addends. Unfractionated serum caused a rapid bleaching of MeG(+) and MG(+), while PR(+) and CV(+) were unaffected. Sephacryl S200 HR chromatographic screening of the serum revealed two composite peaks of MeG(+)-bleaching activity. The major peak (M(r) range, 40,000-130,000) overlapped with and extended on either side of the albumin peak. The minor peak corresponding to ca. 10% of the total MeG(+)-bleaching capacity had M(r) > 230,000. MG(+)-bleaching activity dominated the entire chromatographic profile and implicated a multitude of minority proteins with a high capacity to form colorless MG adducts. It is concluded that highly electrophilic TAM(+)s such as MeG(+) and MG(+) must be quantitatively trapped in the form of dye-protein adducts in biological fluids and that the primary in vivo effects (e.g. toxicity) of such dyes most likely arise from ligand-type effects on multiple protein targets. Mechanisms that call for unmodified TAM(+) structure (radical-mediated redox changes, DNA intercalation) may be more relevant to the in vivo impact of dyes such as PR(+) and CV(+) that have a lower tendency to form adducts. (c) 2004 Wiley Periodicals, Inc. J Biochem Mol Toxicol 18:253-256, 2004 Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.20034.
机译:四种阳离子三芳基甲烷染料(TAM(+)s),甲基绿(MeG(+)),孔雀石绿(MG(+)),对硝基苯胺(PR(+))和结晶紫(CV( +))是在25 mC,50 mM 3-(N-吗啉代)丙烷磺酸(MOPS)缓冲液(pH 8)中分光光度法研究的,方法是在不存在和存在人血清的情况下监测TAM(+)颜色的损失蛋白质作为潜在的附加物。普通血清引起MeG(+)和MG(+)的快速漂白,而PR(+)和CV(+)则不受影响。血清的Sephacryl S200 HR色谱筛选显示了MeG(+)漂白活性的两个复合峰。主峰(M(r)范围40,000-130,000)与白蛋白峰的两侧重叠并延伸。对应于ca的次要峰。 MeG(+)漂白总容量的10%的M(r)> 230,000。 MG(+)漂白活性主导了整个色谱图,并暗示了许多具有形成无色MG加合物的高容量的少数蛋白质。结论是,高度亲电的TAM(+)(例如MeG(+)和MG(+))必须以染料-蛋白质加合物的形式定量地捕获在生物体液中,并且此类化合物的主要体内效应(例如毒性)染料最有可能是由对多种蛋白质靶标的配体型作用引起的。要求未修饰的TAM(+)结构(自由基介导的氧化还原变化,DNA嵌入)的机制可能与染料(如PR(+)和CV(+))形成加合物的可能性较低的体内影响更为相关。 。 (c)2004 Wiley Periodicals,Inc. J Biochem Mol Toxicol 18:253-256,2004,在线发布在Wiley InterScience(www.interscience.wiley.com)上。 DOI 10.1002 / jbt.20034。

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