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A review on structure-affinity relationship of dietary flavonoids with serum albumins

机译:膳食类黄酮与血清白蛋白的结构亲和性研究进展

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摘要

Flavonoids are a class of plant secondary metabolites and among thousands of flavonoids few are considered as dietary flavonoids. Serum albumin (SA), the most abundant protein in plasma, functions as the most important carrier of vital drugs, including dietary flavonoids. The binding affinity of dietary flavonoids to SA is demonstrated to be governed by structure-affinity relationship (SAR) and its bioavailability. The present review summarizes the interactions of flavonoids categorized as flavanol, flavonol, flavone, isoflavone, flavanones, and anthocyanidins with SAs (bovine serum albumin and human serum albumin) in light of SAR. The key findings are: (1) the position and degree of hydroxylation highly influence the affinity of flavonoids to SAs, (2) glycosylation decreases and substitution of methoxy group increases the affinity of flavonoids for SAs, (3) catechin gallates have higher binding affinity to SAs than catechins and gallocatechins, (4) inorganic metal ions modulate the binding affinity of flavonoids to SAs, and (5) hydrophobic interaction plays a major role in the interactions of all flavonoids with SAs.
机译:类黄酮是植物次生代谢产物的一类,在数千种类黄酮中,很少有人将其视为饮食类黄酮。血浆白蛋白(SA)是血浆中最丰富的蛋白质,是重要的重要药物载体,包括膳食类黄酮。膳食类黄酮对SA的结合亲和力证明受结构亲和关系(SAR)及其生物利用度的支配。本综述总结了SAR引起的类黄酮,黄酮醇,黄酮,异黄酮,黄酮和花色素苷与SAs(牛血清白蛋白和人血清白蛋白)的相互作用。关键发现是:(1)羟基化的位置和程度极大地影响了类黄酮对SAs的亲和力;(2)糖基化作用降低,甲氧基取代增加了类黄酮对SAs的亲和力;(3)儿茶素没食子酸酯具有更高的结合亲和力与儿茶素和加洛卡菌素相比,它们对SA的作用更大;(4)无机金属离子调节类黄酮对SA的结合亲和力;(5)疏水相互作用在所有类黄酮与SA的相互作用中起主要作用。

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