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Protein stability regulators screeningassay (Pro-SRSA): protein degradation meets theCRISPR-Cas9 library 被引量:1

Protein stability regulators screening assay(Pro-SRSA):protein degradation meets the CRISPR-Cas9 library
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摘要 The regulation of protein stability is a fundamental issue for biophysical processes,but there has not previously been a convenient and unbiased method of identifying regulators of protein stability.However,as reported in the article entitled "A genome-scale CRISPR-Cas9 screening method for protein stability reveals novel regulators of Cdc25 A," recently published in Cell Discovery,our team developed a protein stability regulators screening assay(Pro-SRSA) by combining the whole-genome clustered regularly interspaced short palindromic repeats Cas9(CRISPR-Cas9) library with a dual-fluorescence-based protein stability reporter and high-throughput sequencing to screen for regulators of protein stability.Based on our findings,we are confident that this efficient and unbiased screening method at the genome scale will be used by researchers worldwide to identify regulators of protein stability. The regulation of protein stability is a fundamental issue for biophysical processes, but there has not previously beena convenient and unbiased method of identifying regulators of protein stability. However, as reported in the articleentitled “A genome-scale CRISPR-Cas9 screening method for protein stability reveals novel regulators of Cdc25A,”recently published in Ce// Dhcovery, our team developed a protein stability regulators screening assay (Pro-SRSA) bycombining the whole-genome clustered regularly interspaced short palindromic repeats Cas9 (CRISPR-Cas9) librarywith a dual-fluorescence-based protein stability reporter and high-throughput sequencing to screen for regulatorsof protein stability. Based on our findings, we are confident that this efficient and unbiased screening method at thegenome scale will be used by researchers worldwide to identify regulators of protein stability.
出处 《Chinese Journal of Cancer》 SCIE CAS CSCD 2016年第8期385-387,共3页
基金 supported by grants from the Key Project of Guangzhou(No.1561000151) the Yangtze River Scholarship(No.85000-52121100) the National Nature Science Foundation in China(No.81530081,31571395) the 973 project(No.2012CB967000)
关键词 CRISPR-Cas9 screening Protein stability Cdc25A Ubiquitination ACETYLATION CRISPR-Cas9 screening, Protein stability, Cdc25A, Ubiquitination, Acetylation
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