Wei Wei, Shin Young Shik, Ma Chao, Wang Jun, Elitas Meltem, Fan Rong, Heath James R
NanoSystems Biology Cancer Center, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA ; Department of Applied Physics and Materials Science, California Institute of Technology, Pasadena, CA 91125, USA.
NanoSystems Biology Cancer Center, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Genome Med. 2013 Aug 29;5(8):75. doi: 10.1186/gm479. eCollection 2013.
Single-cell functional proteomics assays can connect genomic information to biological function through quantitative and multiplex protein measurements. Tools for single-cell proteomics have developed rapidly over the past 5 years and are providing approaches for directly elucidating phosphoprotein signaling networks in cancer cells or for capturing high-resolution snapshots of immune system function in patients with various disease conditions. We discuss advances in single-cell proteomics platforms, with an emphasis on microchip methods. These methods can provide a direct correlation of morphological, functional and molecular signatures at the single-cell level. We also provide examples of how those platforms are being applied to both fundamental biology and clinical studies, focusing on immune-system monitoring and phosphoprotein signaling networks in cancer.
单细胞功能蛋白质组学分析可通过定量和多重蛋白质测量将基因组信息与生物学功能联系起来。在过去5年中,单细胞蛋白质组学工具发展迅速,为直接阐明癌细胞中的磷酸化蛋白信号网络或捕捉各种疾病状态患者免疫系统功能的高分辨率快照提供了方法。我们讨论了单细胞蛋白质组学平台的进展,重点是微芯片方法。这些方法可以在单细胞水平上提供形态、功能和分子特征的直接关联。我们还提供了这些平台如何应用于基础生物学和临床研究的示例,重点是癌症中的免疫系统监测和磷酸化蛋白信号网络。