清脆的
核酸
DNA
计算生物学
基因组编辑
核酸检测
生物
纳米技术
遗传学
材料科学
基因
作者
Cameron Myhrvold,Catherine A. Freije,Jonathan S. Gootenberg,Omar O. Abudayyeh,Hayden C. Metsky,Ann Durbin,Max J. Kellner,Amanda L. Tan,Lauren M. Paul,Leda Parham,Kimberly García,Kayla G. Barnes,Bridget Chak,Adriano Mondini,Maurício Lacerda Nogueira,Sharon Isern,Scott F. Michael,Ivette Lorenzana,Nathan L. Yozwiak,Bronwyn MacInnis
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-04-26
卷期号:360 (6387): 444-448
被引量:1218
标识
DOI:10.1126/science.aas8836
摘要
Taking CRISPR technology further CRISPR techniques are allowing the development of technologies for nucleic acid detection (see the Perspective by Chertow). Taking advantages of the distinctive enzymatic properties of CRISPR enzymes, Gootenberg et al. developed an improved nucleic acid detection technology for multiplexed quantitative and highly sensitive detection, combined with lateral flow for visual readout. Myhrvold et al. added a sample preparation protocol to create a field-deployable viral diagnostic platform for rapid detection of specific strains of pathogens in clinical samples. Cas12a (also known as Cpf1), a type V CRISPR protein, cleaves double-stranded DNA and has been adapted for genome editing. Chen et al. discovered that Cas12a also processes single-stranded DNA threading activity. A technology platform based on this activity detected human papillomavirus in patient samples with high sensitivity. Science , this issue p. 439 , p. 444 , p. 436 ; see also p. 381
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