Department of Analytical Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, Heyrovského 1203/8, 500 05 Hradec Králové, Czech Republic.
Department of Biology, Faculty of Science, University of Hradec Králové, Hradecká 1285, 500 03 Hradec Králové, Czech Republic.
Anal Chem. 2023 Aug 22;95(33):12339-12348. doi: 10.1021/acs.analchem.3c01772. Epub 2023 Aug 11.
Sample preparation involving the cleavage of proteins into peptides is the first critical step for successful bottom-up proteomics and protein analyses. Time- and labor-intensiveness are among the bottlenecks of the commonly used methods for protein sample preparation. Here, we report a fast online method for postinjection acid cleavage of proteins directly in the mobile phase typically used for LC-MS analyses in proteomics. The chemical cleavage is achieved in 0.1% formic acid within 35 s in a capillary heated to 195 °C installed upstream of the analytical column, enabling the generated peptides to be separated. The peptides generated by the optimized method covered the entire sequence except for one amino acid of trastuzumab used for the method development. The qualitative results are extraordinarily stable, even over a long period of time. Moreover, the method is also suitable for accurate and repeatable quantification. The procedure requires only one manual step, significantly decreasing sample transfer losses. To demonstrate its practical utility, we tested the method for the fast detection of ricin. Ricin can be unambiguously identified from an injection of 10 ng, and the results can be obtained within 7-8 min after receiving a suspicious sample. Because no sophisticated accessories and no additional reagents are needed, the method can be seamlessly transferred to any laboratory for high-throughput proteomic workflows.
样品制备涉及蛋白质肽段的酶切,这是成功进行基于自上而下的蛋白质组学和蛋白质分析的关键步骤之一。常用蛋白质样品制备方法的时间和劳动强度是其面临的瓶颈之一。在这里,我们报告了一种快速的在线方法,用于在毛细管中直接在通常用于蛋白质组学 LC-MS 分析的流动相内进行注射后酸酶切。在安装于分析柱上游的、加热至 195°C 的毛细管中,在 0.1%甲酸中于 35 秒内实现化学酶切,使生成的肽段能够被分离。该优化方法生成的肽段覆盖了除用于方法开发的曲妥珠单抗外的整个序列。即使经过很长一段时间,定性结果也非常稳定。此外,该方法也适用于准确和可重复的定量。该方法仅需手动操作一步,大大减少了样品转移损失。为了证明其实际应用,我们使用该方法快速检测蓖麻毒素。只需注射 10ng 即可明确鉴定出蓖麻毒素,在收到可疑样品后 7-8 分钟即可获得结果。由于不需要复杂的附件和额外的试剂,该方法可以无缝转移到任何实验室进行高通量蛋白质组学工作流程。