▎ 摘　　要

Protein digestion and isotope, labeling are two critical steps in proteome quantification. However, the conventional in-solution protocol unavoidably suffers from disadvantages such as time-consuming, low labeling efficiency, and tedious off-line manual operation, which might affect the quantification accuracy, reproducibility, and throughput. To address these problems, we developed a fully automated proteome quantification platform, in which an ultraperformance immobilized microreactor (upIMER) with graphene-oxide-modified polymer micro spheres as the matrix was developed, to achieve not only the simultaneous protein digestion and O-18 labeling, but also the online integration, with nano-high-pressure liquid chromatography electrospray ionization-tandem mass spectrometry (nanoHPLC ESI-MS/MS). Compared to the conventional off-line protocols, such a platform exhibits obviously improved digestion and O-18 labeling efficiency (only 8% peptides with missed cleavage sites, 99% labeling efficiency, and 2.5 min reaction time), leading to the increased quantification coverage, accuracy, precision and throughput. All the results demonstrated that our developed fully automated platform should provide new opportunities to improve the accuracy, reproducibility, and throughput for proteome quantification.