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Binding Activity of Prokaryotic Argonaute for Background-Suppressed Exponential Isothermal Amplification.
Lin, Qiuyuan; Ye, Xin; Chen, Hongyuan; Fang, Xueen; Chen, Hui; Kong, Jilie.
Afiliação
  • Lin Q; Department of Laboratory Medicine, Key Laboratory of Clinical Laboratory Technology for Precision Medicine, School of Medical Technology and Engineering Fujian Medical University, Fuzhou 350005, China.
  • Ye X; Department of Laboratory Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, Shaanxi PR China.
  • Chen H; State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai 200437, China.
  • Fang X; Department of Chemistry, Fudan University, Shanghai 200437, China.
  • Chen H; Department of Chemistry, Fudan University, Shanghai 200437, China.
  • Kong J; Department of Chemistry, Fudan University, Shanghai 200437, China.
Anal Chem ; 96(2): 620-623, 2024 01 16.
Article em En | MEDLINE | ID: mdl-38170960
ABSTRACT
Prokaryotic Argonautes (pAgos) have been recently used in many nucleic acid biosensing applications but have rarely been used for regulating the isothermal amplification system. Herein, we reported Thermus thermophilus Argonaute (TtAgo)-mediated background-suppressed exponential isothermal amplification (EXPAR) as the first example to explore the binding activity of pAgos toward regulation of the amplification template. It was demonstrated that thermophilic pAgos efficiently eliminated nonspecific hybridization between templates by their binding affinity with the template, resulting in greatly enhancing the specificity of EXPAR. TtAgo-mediated, background-suppressed EXPAR was employed to detect miRNA with a detection limit of 10-15 M, which was 1000 times and 100 times more sensitive than that of traditional RT-PCR and EXPAR, respectively. This method further showed good performance in discriminating cancer patients from healthy individuals, indicating its potential for practical clinical applications.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs Idioma: En Ano de publicação: 2024 Tipo de documento: Article