Division of Clinical Protein Science and Imaging, Department of Clinical Sciences (Lund) and Department of Biomedical Engineering , Lund University , SE-221 84 Lund , Sweden.
Department of Clinical Sciences Lund (Surgery) , Lund University, and Skåne University Hospital , SE-221 84 Lund , Sweden.
J Proteome Res. 2018 Jul 6;17(7):2556-2561. doi: 10.1021/acs.jproteome.8b00228. Epub 2018 Jun 7.
Urea-containing buffer solutions are generally used in proteomic studies to aid protein denaturation and solubilization during cell and tissue lysis. It is well-known, however, that urea can lead to carbamylation of peptides and proteins and, subsequently, incomplete digestion of proteins. By the use of cells and tissues that had been lysed with urea, different solution digestion strategies were quantitatively assessed. In comparison with traditional proteolysis at 37 °C, urea in-solution digestion performed at room temperature improved peptide and protein identification and quantitation and had a minimum impact on miscleavage rates. Furthermore, the signal intensities and the number of carbamylated and pyroglutamic acid-modified peptides decreased. Overall, this led to a reduction in the negative effects often observed for such modifications. Data are available via ProteomeXchange with identifier PXD009426.
含尿素的缓冲溶液通常用于蛋白质组学研究中,以辅助细胞和组织裂解过程中蛋白质的变性和溶解。然而,众所周知,尿素会导致肽和蛋白质的氨甲酰化,从而导致蛋白质不完全消化。通过使用已经用尿素裂解的细胞和组织,定量评估了不同的溶液消化策略。与传统的 37°C 蛋白酶解相比,在室温下进行的尿素溶液消化可提高肽和蛋白质的鉴定和定量,并且对错误切割率的影响最小。此外,信号强度以及氨甲酰化和焦谷氨酸修饰肽的数量减少。总的来说,这减少了此类修饰通常带来的负面影响。数据可通过 ProteomeXchange 以标识符 PXD009426 获得。