Wiest Nathaniel E, Tomkinson Alan E
University of New Mexico School of Medicine, Albuquerque, NM, United States.
University of New Mexico School of Medicine, Albuquerque, NM, United States.
Methods Enzymol. 2017;591:1-32. doi: 10.1016/bs.mie.2017.03.001. Epub 2017 May 3.
The isolation of proteins on nascent DNA (iPOND) technique developed by the Cortez laboratory allows a previously unparalleled ability to examine proteins associated with replicating and newly synthesized DNA in mammalian cells. Both the original, formaldehyde-based iPOND technique and a more recent derivative, accelerated native iPOND (aniPOND), have mostly been performed in adherent cell lines. Here, we describe modifications to both protocols for use with suspension cell lines. These include cell culture, pulse, and chase conditions that optimize sample recovery in both protocols using suspension cells and several key improvements to the published aniPOND technique that reduce sample loss, increase signal to noise, and maximize sample recovery. Additionally, we directly and quantitatively compare the iPOND and aniPOND protocols to test the strengths and limitations of both. Finally, we present a detailed protocol to perform the optimized aniPOND protocol in suspension cell lines.
科尔特斯实验室开发的新生DNA上蛋白质分离(iPOND)技术,使人们具备了前所未有的能力,可在哺乳动物细胞中检测与复制及新合成DNA相关的蛋白质。最初基于甲醛的iPOND技术及其最新衍生技术——加速天然iPOND(aniPOND),大多是在贴壁细胞系中进行的。在此,我们描述了针对这两种方案所做的修改,以便用于悬浮细胞系。这些修改包括细胞培养、脉冲和追踪条件,它们能在使用悬浮细胞的两种方案中优化样品回收率,以及对已发表的aniPOND技术进行的几项关键改进,这些改进可减少样品损失、增加信噪比并最大化样品回收率。此外,我们直接并定量地比较了iPOND和aniPOND方案,以测试两者的优缺点。最后,我们给出了在悬浮细胞系中执行优化后的aniPOND方案的详细步骤。