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                                                              ChromoTek的Nano-Traps具有非凡的IP/ Co-IP性能

                                                              瀏覽次數(shù):550 發(fā)布日期:2017-9-26  來源:本站 僅供參考,謝絕轉(zhuǎn)載,否則責(zé)任自負(fù)

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                                                              圖一.jpg

                                                               

                                                                  On-bead Digestion:從免疫沉淀到質(zhì)譜分析

                                                                  免疫沉淀蛋白及其相互作用物到質(zhì)譜分析的轉(zhuǎn)移率應(yīng)盡可能高。這對(duì)于低豐度的蛋白質(zhì)尤其重要。

                                                                  通過使用on-bead-digestion,您能夠:

                                                                ·節(jié)省時(shí)間——你不需要洗提結(jié)合蛋白質(zhì)

                                                                ·保持蛋白質(zhì)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

                                                                

                                                              圖2.胰蛋白酶.jpg

                                                               

                                                                胰蛋白酶

                                                                對(duì)Nano-Traps (GFP-Trap, RFP-Trap, mNeonGreen-Trap, MBP-Trap, GST-Trap,等)的消化會(huì)產(chǎn)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(dǎo)致的。例如,用胰蛋白酶對(duì)GFP-Trap進(jìn)行on-bead-digestion只產(chǎn)生4個(gè)縮氨酸。

                                                                這并不是唯一的優(yōu)勢(shì):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?nèi)狈贵w輕鏈,產(chǎn)生更純粹的IP/ Co-IP結(jié)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(qǐng)點(diǎn)擊下方查看:

                                                                

                                                              圖3.下載說明書.jpg

                                                                參考文獻(xiàn):

                                                                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

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