仿形(计算机编程)
蛋白质组学
纳米颗粒
纳米技术
等离子体
化学
计算生物学
计算机科学
材料科学
生物
物理
生物化学
量子力学
基因
操作系统
作者
Che‐Fan Huang,Michael A. R. Hollas,Aniel Sánchez,M. Bhattacharya,Giang Ho,Ambika Sundaresan,Michael A. Caldwell,Xiaoyan Zhao,Ryan W. Benz,Asim Siddiqui,Neil L. Kelleher
标识
DOI:10.1021/acs.jproteome.4c00621
摘要
The dynamic range challenge for the detection of proteins and their proteoforms in human plasma has been well documented. Here, we use the nanoparticle protein corona approach to enrich low-abundance proteins selectively and reproducibly from human plasma and use top-down proteomics to quantify differential enrichment for the 2841 detected proteoforms from 114 proteins. Furthermore, nanoparticle enrichment allowed top-down detection of proteoforms between ∼1 μg/mL and ∼10 pg/mL in absolute abundance, providing up to a 10
科研通智能强力驱动
Strongly Powered by AbleSci AI