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Granulomorphometry: A suitable tool for identifying hydrophobic and disulfide bonds in β-lactoglobulin aggregates. Application to the study of β-lactoglobulin aggregation mechanism between 70 and 95℃

机译:颗粒形态计量学:一种鉴定β-乳球蛋白聚集体中疏水键和二硫键的合适工具。在70-95℃之间β-乳球蛋白聚集机理研究中的应用

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摘要

This work deals with the investigation of β-lactoglobulin (β-LG) aggregation by granulomorphometry. In the first part of this study, we showed that the binding interactions involved in aggregate structure could be identified by their appearance in granulomorphometric pictures. The reliability of this analytical approach was demonstrated by comparing the appearance of P-LG aggregates in the presence and absence of a thiol-blocking agent (iV-ethylmaleimide). The translucency of the aggregates was associated with hydrophobic interactions and their opacity was associated with disulfide bonds. We state, based on the morphology of the aggregates, along with the color of protein aggregates and insoluble materials, that hydrophobic interactions had a better water-holding capacity than disulfide bonds. Additionally, our results suggest that disulfide and hydrophobic bonds compete for β-LG aggregate shaping. In the second part of this work, interesting features of granulomorphometry useful for identifying aggregate binding interactions were highlighted to clarify the effect of temperature on the aggregation mechanisms occurring in a β-LG concentrate with a moderate calcium content (6.6 mmol-L~(-1)). Heat treatment experiments were performed between 70 and 95℃, and granulomorphometric measurements (aggregate size, aggregate number, and gray level of the picture) were conducted at different sampling times up to 4 h. Results, which were interpreted in light of calculated β-LG denaturation levels, revealed that the aggregation mechanism could be split into 2 steps. Initially, β-LG denatured quickly, leading to fast β-LG aggregation by disulfide bonds. The denaturation rate then declined, which drastically slowed the disulfide aggregation mechanism. From that point on, a second aggregation path became preponderant. It consisted of the agglomeration of small aggregates by hydrophobic interactions and resulted in the formation of large aggregates containing both interaction types. This second aggregation mechanism was clearly favored at high temperatures because it was not detected in our experiments at temperatures below 85℃.
机译:这项工作涉及通过颗粒形态测定法研究β-乳球蛋白(β-LG)聚集。在这项研究的第一部分中,我们表明聚集结构中涉及的结合相互作用可以通过其在颗粒形态学图中的出现来识别。通过比较在存在和不存在硫醇封闭剂(IV-乙基马来酰亚胺)下P-LG聚集体的外观,证明了这种分析方法的可靠性。聚集体的半透明性与疏水相互作用有关,其不透明性与二硫键有关。根据聚集体的形态,以及蛋白质聚集体和不溶性物质的颜色,我们认为疏水性相互作用比二硫键具有更好的持水能力。此外,我们的结果表明,二硫键和疏水键竞争β-LG聚集体的形成。在这项工作的第二部分中,突出了颗粒形态计量学的有趣特征,可用于识别聚集体结合相互作用,以阐明温度对中等钙含量(6.6 mmol-L〜(- 1))。在70至95℃的温度范围内进行了热处理实验,并在长达4小时的不同采样时间进行了粒度形态测量(骨料尺寸,骨料数量和图片的灰度级)。根据计算的β-LG变性水平对结果进行解释,结果表明聚集机理可以分为两个步骤。最初,β-LG迅速变性,通过二硫键导致快速的β-LG聚集。然后变性速率下降,这大大减慢了二硫键的聚集机理。从那时起,第二条聚合路径成为优势。它由疏水作用引起的小聚集体的团聚组成,并导致包含两种相互作用类型的大聚集体的形成。第二种聚集机制在高温下显然是有利的,因为在我们的实验中,温度低于85℃时未检测到它。

著录项

  • 来源
    《Journal of dairy science》 |2012年第8期|p.4188-4202|共15页
  • 作者单位

    INRA UR638-Processus aux Interfaces et Hygiene des Materiaux, BP 20039, 59651 Villeneuve d'Ascq Cedex, France;

    INRA UR638-Processus aux Interfaces et Hygiene des Materiaux, BP 20039, 59651 Villeneuve d'Ascq Cedex, France;

    INRA UR638-Processus aux Interfaces et Hygiene des Materiaux, BP 20039, 59651 Villeneuve d'Ascq Cedex, France;

    INRA UR638-Processus aux Interfaces et Hygiene des Materiaux, BP 20039, 59651 Villeneuve d'Ascq Cedex, France;

    INRA UR638-Processus aux Interfaces et Hygiene des Materiaux, BP 20039, 59651 Villeneuve d'Ascq Cedex, France;

    INRA UR638-Processus aux Interfaces et Hygiene des Materiaux, BP 20039, 59651 Villeneuve d'Ascq Cedex, France;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    granulomorphometry; β-lactoglobulin; disulfide bond; hydrophobic interaction;

    机译:颗粒形态β-乳球蛋白;二硫键疏水相互作用;

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