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鉴定源自初始4-氧代-2-壬烯醛-半胱氨酸迈克尔加成物的高级反应产物。

Identification of advanced reaction products originating from the initial 4-oxo-2-nonenal-cysteine Michael adducts.

作者信息

Shimozu Yuuki, Shibata Takahiro, Ojika Makoto, Uchida Koji

机构信息

Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.

出版信息

Chem Res Toxicol. 2009 May;22(5):957-64. doi: 10.1021/tx900059k.

Abstract

4-Oxo-2-nonenal (ONE), an aldehyde originating from the peroxidation of omega6 polyunsaturated fatty acids, preferentially reacts with the cysteine residues of protein. Despite the fact that there has been significant recent interest in the protein reactivity and biological activity of ONE, the structural basis of the ONE-cysteine adducts remain to be established. In the present study, to gain a structural insight into the sulfhydryl modification by ONE, we characterized reaction products that originated from the initial ONE-cysteine Michael adducts. N-Acetyl-L-cysteine (10 mM) was incubated with an equimolar concentration of ONE in 0.1 M phosphate buffer (pH 7.4) at 37 degrees C. Within 1 h of incubation, the reaction of N-acetyl-L-cysteine with ONE resulted in the formation of two (C-2 and C-3) Michael addition products possessing a carbonyl functionality. Subsequent incubation of the reaction mixture resulted in their disappearance and concomitant formation of advanced reaction products, including a minor product III and major products IVa, IVb, and V. Product III was identified to be a thiomorpholine derivative, 4-acetyl-5-hydroxyl-6-(2-oxoheptyl)thiomorpholine-3-carboxylic acid, which might have originated from the C-2 Michael addition product. The major products were identified to be the novel 2-cyclopentenone derivatives, that is, 2-(acetylamino)-3-[(3-butyl-4-oxocyclopent-2-en-1-yl)sulfanyl]propionic acid (IVa and its isomer IVb) and 2-(acetylamino)-3-[(4-butyl-5-oxocyclopent-3-en-1-yl)sulfanyl]propionic acid (V), which might be generated through the base-catalyzed cyclization of the C-2 and C-3 Michael addition products, respectively. The furan derivative, which has been reported as the end product of the Michael adducts, was found to be formed only under acidic conditions. Thus, this study identified the novel ONE-cysteine adducts, including the most prominent 2-cyclopentenone derivatives, that originated from the initial Michael adducts.

摘要

4-氧代-2-壬烯醛(ONE)是一种源自ω-6多不饱和脂肪酸过氧化反应的醛类物质,它优先与蛋白质的半胱氨酸残基发生反应。尽管近期人们对ONE的蛋白质反应活性和生物活性产生了浓厚兴趣,但ONE与半胱氨酸加合物的结构基础仍有待确定。在本研究中,为了深入了解ONE对巯基的修饰作用,我们对源自最初的ONE-半胱氨酸迈克尔加成产物的反应产物进行了表征。将N-乙酰-L-半胱氨酸(10 mM)与等摩尔浓度的ONE在0.1 M磷酸盐缓冲液(pH 7.4)中于37℃孵育。孵育1小时内,N-乙酰-L-半胱氨酸与ONE的反应生成了两种具有羰基官能团的迈克尔加成产物(C-2和C-3)。随后对反应混合物进行孵育,这两种产物消失,并同时形成了高级反应产物,包括次要产物III和主要产物IVa、IVb和V。产物III被鉴定为硫代吗啉衍生物,即4-乙酰基-5-羟基-6-(2-氧代庚基)硫代吗啉-3-羧酸,它可能源自C-2迈克尔加成产物。主要产物被鉴定为新型的2-环戊烯酮衍生物,即2-(乙酰氨基)-3-[(3-丁基-4-氧代环戊-2-烯-1-基)硫烷基]丙酸(IVa及其异构体IVb)和2-(乙酰氨基)-3-[(4-丁基-5-氧代环戊-3-烯-1-基)硫烷基]丙酸(V),它们可能分别是通过C-2和C-3迈克尔加成产物的碱催化环化反应生成的。据报道作为迈克尔加成产物终产物的呋喃衍生物,仅在酸性条件下形成。因此,本研究鉴定了源自最初迈克尔加成产物的新型ONE-半胱氨酸加合物,包括最主要的2-环戊烯酮衍生物。

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