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ATP Binding Cassette Transporter A1 Regulates the Lipid Raft Proteome of the Resting and Lipopolysaccharide-stimulated Macrophage

机译:ATP粘合盒传输器A1调节静止和脂多糖刺激的巨噬细胞的脂质筏蛋白质组

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A semi-quantitative spectral counting approach was initially evaluated to study expression changes in lipid raft proteins of Abca1~(+/+) and Abca1~(-/-) bone marrow macrophages after LPS exposure. Two biological preparations showed significant variability. LC-MS/MS data indicate that several proteins are differentially up- or down-regulated in rafts from Abca1~(+/+) and Abca1~(-/-) macrophages. Further exploration of new biological replicates is underway to confidently define the global raft proteome and its dependence upon ABCA1 expression and LPS exposure. For better quantitation and confidence, a SILAC-based analysis of Abca1~(+/+) and Abca1~(-/-) bone marrow macrophages after LPS exposure is in progress.
机译:最初评价半定量光谱计数方法,以在LPS暴露后研究ABCA1〜(+ / +)和ABCA1〜( - / - )骨髓巨噬细胞的脂质筏蛋白中的表达变化。两种生物制剂显示出显着的变化。 LC-MS / MS数据表明,几种蛋白质在来自ABCA1〜(+ / +)和ABCA1〜( - / - )巨噬细胞的筏中的差异上调或下调。正在进一步探索新的生物学重复,以自信地定义全球筏蛋白质组及其对ABCA1表达和LPS暴露的依赖性。为了更好的定量和置信度,在LPS暴露后,ABCA1〜(+ / +)和ABCA1〜( - / - / - )骨髓巨噬细胞的基于硅酸基因分析。

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