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Using Tumor Explants for Imaging Mass Spectrometry Visualization of Unlabeled Peptides and Small Molecules

机译:使用肿瘤外植体进行成像肽和小分子的质谱可视化

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Matrix assisted laser desorption ionization time-of-flight (MALDI-TOF) imaging mass spectrometry has emerged as a powerful, label-free technique to visualize penetration of small molecules in vivo and in vitro , including in 3D cell culture spheroids; however, some spheroids do not grow sufficiently large to provide enough area for imaging mass spectrometry. Here, we describe an ex vivo method for visualizing unlabeled peptides and small molecules in tumor explants, which can be divided into pieces of desired size, thus circumventing the size limitations of many spheroids. As proof-of-concept, a small molecule drug (4-hydroxytamoxifen), as well as a peptide drug (cyclosporin A) and peptide chemical probe, can be visualized after in vitro incubation with tumor explants so that this technique may provide a solution to robing cell penetration by unlabeled peptides.
机译:基质辅助激光解吸电离飞行时间(MALDI-TOF)成像质谱已经出现为一种强大的无标记技术,可视化体内体内小分子的渗透和在体外,包括3D细胞 培养球体; 然而,一些球状体不会足够大,以提供足够的成像质谱法。 在这里,我们描述了一种用于可视化未标记的肽和肿瘤外部植物中的小分子的诸如肿瘤外植物的诸如所需尺寸的小分子,从而绕过许多球状体的尺寸限制。 作为概念证据,可以在与肿瘤外植体的体外培养后可以通过肽药物(4-羟基氧基毒素)以及肽药物(环孢菌素A)和肽化学探针。 通过未标记的肽提供抢夺细胞渗透的解决方案。

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