On-bead Digestion:從免疫沉淀到質譜分析

　　  免疫沉淀蛋白及其相互作用物到質譜分析的轉移率應盡可能高。這對于低豐度的蛋白質尤其重要。

　　  通過使用on-bead-digestion,您能夠：

　　·節省時間——你不需要洗提結合蛋白質

　　·保持蛋白質高濃度——不要稀釋你的樣品

　　·更少的洗滌步驟能更好的保留Co-IP的相互作用物

　　胰蛋白酶

　　對Nano-Traps (GFP-Trap, RFP-Trap, mNeonGreen-Trap, MBP-Trap, GST-Trap,等)的消化會產生少量的縮氨酸。這是由于固定化的羊駝抗體的小尺寸(14 kDa)導致的。例如，用胰蛋白酶對GFP-Trap進行on-bead-digestion只產生4個縮氨酸。

　　這并不是*的優勢:由于它們的高親和力和低背景，ChromoTek的Nano-Traps具有非凡的IP/ Co-IP性能。

　　ChromoTek的Nano-Traps是分離自羊駝單域抗體(VHHs，也稱為納米體)。因此，它們缺乏抗體輕鏈，產生更純粹的IP/ Co-IP結果。

　　„The best results were obtained by direct tryptic digest of the material on beads followed by mass spectrometry”, Zoltan Lipinszki et al. (2014)

　　ChromoTek GFP-Trap的on-bead-digestion protocol請點擊下方查看：

　　參考文獻：

　　1. Arne H. Smits, Pascal W. T. C. Jansen, Ina Poser, Anthony A. Hyman, Michiel Vermeulen; Stoichiometry of chromatin-associated protein complexes revealed by label-free quantitative mass spectrometry-based proteomics. Nucleic Acids Res 2013; 41 (1): e28. doi: 10.1093/nar/gks941

　　2. Zoltan Lipinszki, Peng Wang, Rhys Grant, Catherine Lindon, Nikola S. Dzhindzhev, Pier Paolo D’Avino, Marcin R. Przewloka, David M. Glover, Vincent Archambault; Affinity Purification of Protein Complexes from Drosophila Embryos in Cell Cycle Studies. Methods Mol Biol. 2014;1170:571-88. doi: 10.1007/978-1-4939-0888-2_33.

　　3. Susan L. Kloet, Matthew M. Makowski, H. Irem Baymaz, Lisa van Voorthuijsen, Ino D. Karemaker, Alexandra Santanach, Pascal W.T.C. Jansen, Luciano Di Croce, Michiel Vermeulen; The dynamic interactome and genomic targets of Polycomb complexes during stem cell differentiation. Nat Struct Mol Biol. 2016 July ; 23(7): 682–690. doi:10.1038/nsmb.3248

　　4. Benedetta Turriziani, Amaya Garcia-Munoz, Ruth Pilkington, Cinzia Raso, Walter Kolch, Alexander von Kriegsheim; On-Beads Digestion in Conjunction with Data-Dependent Mass Spectrometry: A Shortcut to Quantitative and Dynamic Interaction Proteomics. Biology 2014, 3(2), 320-332; doi:10.3390/biology3020320