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Identification of Peroxisome Proliferation BioMarkers by SELDI/ProteinChip Arrays

机译:Seldi / Proteinchip阵列鉴定过氧化物酶体增殖生物标志物

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1. SELDI/ProteinChip Array system was evaluated for bio-marker identification using wild-type, AOX~(-/-), and Wy14,643 induced mouse liver samples. 2. Screened by four different chip surfaces, the liver protein profile of AOX-/- mice showed similarity with Wy14,643 induced mice, however, significant difference from wild-type mice. 3. A total of forty peaks showed more than 2-fold difference between wild type and treated mouse liver samples. 4. The 18.7-kDa protein was enriched by Q-Saphadex spin column and further purified from SDS-PAGE gel for tryptic digestion. 5. As a proof of principle, tryptic mapping by SELDI identified the 18.7 kDa protein as major urinary protein, which was further confirmed by LC-MS/MS.
机译:使用野生型,AOX〜( - / - )和Wy14,643诱导小鼠肝脏样品评估Seldi / Proteinchip阵列系统进行生物标记识别。 2.通过四种不同的芯片表面筛选,AOX - / - 小鼠的肝蛋白谱与Wy14,643诱导小鼠的相似性,然而,与野生型小鼠的显着差异。 3.共有四十峰在野生型和治疗的小鼠肝脏样品之间显示出超过2倍的差异。 4.通过Q-Saphadex旋转柱富集18.7-KDA蛋白,并从SDS-PAGE凝胶进一步纯化,用于胰蛋白酶消化。 5.作为原理的证据,Seldi的胰蛋白酶映射鉴定了18.7kDa蛋白作为主要尿蛋白,其通过LC-MS / MS进一步证实。

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