David Brian P, Dubrovskyi Oleksii, Speltz Thomas E, Wolff Jeremy J, Frasor Jonna, Sanchez Laura M, Moore Terry W
Department of Medicinal Chemistry and Pharmacognosy and UI Cancer Center, University of Illinois at Chicago, 833 South Wood Street, Chicago, Illinois 60612, United States.
Department of Physiology and Biophysics and UI Cancer Center, University of Illinois at Chicago, 835 South Wolcott, Chicago, Illinois 60623, United States.
ACS Med Chem Lett. 2018 May 17;9(7):768-772. doi: 10.1021/acsmedchemlett.8b00091. eCollection 2018 Jul 12.
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 and , 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 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 incubation with tumor explants so that this technique may provide a solution to robing cell penetration by unlabeled peptides.
基质辅助激光解吸电离飞行时间(MALDI-TOF)成像质谱已成为一种强大的、无需标记的技术,可用于可视化小分子的渗透,包括在三维细胞培养球体中;然而,一些球体生长得不够大,无法为成像质谱提供足够的面积。在这里,我们描述了一种在肿瘤外植体中可视化未标记肽和小分子的方法,肿瘤外植体可以被切成所需大小的碎片,从而规避了许多球体的大小限制。作为概念验证,一种小分子药物(4-羟基他莫昔芬)以及一种肽药物(环孢素A)和肽化学探针,在与肿瘤外植体孵育后可以被可视化,因此该技术可能为未标记肽的细胞穿透研究提供一种解决方案。