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10.1016/j.bios.2020.112867

http://scihub22266oqcxt.onion/10.1016/j.bios.2020.112867
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suck abstract from ncbi


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pmid33303323      Biosens+Bioelectron 2021 ; 175 (ä): 112867
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  • The application of DNA polymerases and Cas9 as representative of DNA-modifying enzymes group in DNA sensor design (review) #MMPMID33303323
  • Dronina J; Bubniene US; Ramanavicius A
  • Biosens Bioelectron 2021[Mar]; 175 (ä): 112867 PMID33303323show ga
  • Rapid detection of nucleic acids (DNA or RNA) by inexpensive, selective, accurate, and highly sensitive methods is very important for biosensors. DNA-sensors based on DNA-modifying enzymes for fast determination and monitoring of pathogenic (Zika, Dengue, SARS-Cov-2 (inducer of COVID-19), human papillomavirus, HIV, etc.) viruses and diagnosis of virus-induced diseases is a key factor of this overview. Recently, DNA-modifying enzymes (Taq DNA polymerase, Phi29 DNA polymerase) have been widely used for the diagnosis of virus or pathogenic disease by gold standard (PCR, qPCR, RT-qPCR) methods, therefore, alternative methods have been reviewed. The main mechanisms of DNA metabolism (replication cycle, amplification) and the genomeediting tool CRISPR-Cas9 are purposefully discussed in order to address strategic possibility to design DNA-sensors based on immobilized DNA-enzymes. However, the immobilization of biologically active proteins on a gold carrier technique with the ability to detect viral or bacterial nucleic acids is individual for each DNA-modifying enzyme group, due to a different number of active sites, C and N terminal locations and arrangement, therefore, individual protocols based on the 'masking' of active sites should be elaborated for each enzyme.
  • |*Biosensing Techniques[MESH]
  • |COVID-19/*diagnosis/genetics/virology[MESH]
  • |CRISPR-Cas Systems/genetics[MESH]
  • |Diagnostic Tests, Routine[MESH]
  • |Humans[MESH]
  • |RNA, Viral/genetics/*isolation & purification[MESH]


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