期刊
ANALYTICAL CHEMISTRY
卷 93, 期 16, 页码 6403-6413出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c05393
关键词
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资金
- National Key Research and Development Program [2017YFA0505001, 2018YFA0507501]
- National Natural Science Foundation of China [81827901]
- innovative research team of highlevel local university in Shanghai
- Improvement of Service Capability for Shanghai Proteomics Professional Technical Platform for Severe Diseases [18DZ2292900]
The PMSNP method was developed for efficient capture and analysis of nascent proteins, achieving a modification efficiency of 91.8% on silica microspheres through click reaction. After optimization, more than 3500 and 3900 nascent proteins could be rapidly identified, demonstrating the sensitivity and immediacy of this method in exploring changes in the translation process.
Nascent proteome is crucial in directly revealing how the expression of a gene is regulated on a translation level. In the nascent protein identification, puromycin capture is one of the pivotal methods, but it is still facing the challenge in the deep profiling of nascent proteomes due to the low abundance of most nascent proteins. Here, we describe the synthesis of puromycin-modified silica microspheres (PMSs) as the sorbent of dispersive solid-phase microextraction and the establishment of the PMS-based nascent proteomics (PMSNP) method for efficient capture and analysis of nascent proteins. The modification efficiency of puromycin groups on silica microspheres reached 91.8% through the click reaction. After the optimization and simplification of PMSNP, more than 3500 and 3900 nascent proteins were rapidly identified in HeLa cells and mouse brains within 13.5 h, respectively. The PMSNP method was successfully applied to explore changes in the translation process in a biological stress model, namely, the lipopolysaccharide-stimulated HeLa cells. Biological functional analyses revealed the unique characters of the nascent proteomes and exhibited the superiority of the PMSNP in the identification of low abundance and secreted nascent proteins, thus demonstrating the sensitivity and immediacy of the PMSNP method.
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