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用于分离和表征细胞外囊泡的正交方法的优化与比较,以研究婴儿配方奶粉对母乳的代表性如何。

Optimisation and comparison of orthogonal methods for separation and characterisation of extracellular vesicles to investigate how representative infant milk formula is of milk.

作者信息

Mukhopadhya Anindya, Santoro Jessie, Moran Barry, Useckaite Zivile, O'Driscoll Lorraine

机构信息

School of Pharmacy and Pharmaceutical Sciences & Trinity Biomedical Sciences Institute, Trinity College Dublin and Trinity St. James's Cancer Institute, Dublin 2, Ireland.

School of Biochemistry & Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.

出版信息

Food Chem. 2021 Aug 15;353:129309. doi: 10.1016/j.foodchem.2021.129309. Epub 2021 Feb 23.

Abstract

Many infants are fed infant milk formula (IMF). However, IMF production from skim milk (SM) involves harsh treatment. So, we hypothesised that the quantity and/or quality of extracellular vesicles (EVs) in IMF may be reduced. Thus, firstly, we aimed to optimise separation of EVs from IMF and SM and, secondly, we aimed to compare the EV isolates from these two sources. Prior to EV isolation, abundant casein micelles of similar sizes to EVs were removed by treating milk samples with either acetic acid or hydrochloric acid. Samples progressed to differential ultracentrifugation (DUC) or gradient ultracentrifugation (GUC). EV characterisation included BCA, SDS-PAGE, nanoparticle tracking (NTA), electron microscopy (TEM), immunoblotting, and imaging flow cytometry (IFCM). Reduced EV concentrations were found in IMF. SM-derived EVs were intact, while IMF contained disrupted EV-like structures. EV biomarkers were more abundant with isolates from SM, indicating EV proteins in IMF are compromised. Altogether, a suitable method combining acid pre-treatment with GUC for EV separation from milk products was developed. EVs appear to be substantially compromised in IMF compared to SM.

摘要

许多婴儿食用婴儿配方奶粉(IMF)。然而,用脱脂牛奶(SM)生产IMF涉及苛刻的处理过程。因此,我们推测IMF中细胞外囊泡(EVs)的数量和/或质量可能会降低。因此,首先,我们旨在优化从IMF和SM中分离EVs的方法,其次,我们旨在比较这两种来源的EV分离物。在分离EVs之前,通过用乙酸或盐酸处理牛奶样品,去除了大量与EVs大小相似的酪蛋白胶束。样品进行差速超速离心(DUC)或梯度超速离心(GUC)。EVs的表征包括BCA、SDS-PAGE、纳米颗粒跟踪分析(NTA)、电子显微镜(TEM)、免疫印迹和成像流式细胞术(IFCM)。结果发现IMF中的EVs浓度降低。SM来源的EVs是完整的,而IMF中含有破坏的类EV结构。与SM分离物相比,EV生物标志物在SM分离物中更为丰富,这表明IMF中的EV蛋白受到了损害。总之,开发了一种将酸预处理与GUC相结合的适合从乳制品中分离EVs的方法。与SM相比,IMF中的EVs似乎受到了很大损害。

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