Table 1.
Nuclease | Platform | Primary amplification method | Detection method | Mechanism | References |
---|---|---|---|---|---|
Cas9 | NASBACC | NASBA | Electronic optical reader | PAM recognition and cleavage to activate Toehead switch | (Pardee et al., 2016) |
CRISDA | PCR | Fluorescence spectrophotometer | Cas9 creates nicks at the border and the target gene amplifies through external primers | (Zhou W. et al., 2018) | |
CAS-EXPAR | EXPAR | Real-time fluoresces monitoring | Cas9 creates nicks and NEase produces ssDNA internal primers cyclically | (Huang et al., 2018) | |
CASLFA | PCR | Paper-based LF device | Cas9/sgRNA complexes with target DNA and detected through AuNP-DNA probes | (Wang et al., 2020) | |
FELUDA | RPA/PCR | Paper-based LF device | gRNA-dFnCas9 RNP complexes with target DNA and detected colorimetric LF device | (Azhar et al., 2020) | |
Cas12 | DETECTR | LAMP | Paper-based LF device | Cas12a-crRNA complex binds and cleaves a dsDNA and detects fluorescence in collateral cleaved probe DNA | (Broughton et al., 2020) |
HOLMES | PCR | Fluorescence spectrophotometer | Cas12a-crRNA complex binds and cleaves a dsDNA and detects fluorescence in collateral cleaved probe DNA | (Li et al., 2018) | |
HOLMESv2 | LAMP | Fluorescence spectrophotometer | HOLMES upgraded; LAMP and Cas12b trans-cleavage integrated into one step | (Li et al., 2019) | |
AIOD-CRISPR | PCR | LED blue light illuminator | One-pot collateral cleavage reaction system and colorimetric detection | (Ding et al., 2020) | |
iSCAN | LAMP | Fluorescence visualization in UV light and LF device | CRISPR-Cas12a-based collateral cleavage and fluorescence-based detection | (Ali et al., 2020) | |
Cas13 | SHERLOCK | RPA | Fluorescence spectrophotometer/ Paper based LF device | crRNA/Cas13 targets an ssRNA and cleaved fluorescent ssRNA probe collaterally | (Gootenberg et al., 2017; Kellner et al., 2020) |
SHERLOCKv2 | RPA | LF device | Upgraded SHERLOCK; High quantification and sensitivity | (Gootenberg et al., 2018) | |
CREST | RPA/PCR | Fluorescence spectrophotometer/Paper based LF device | (Rauch et al., 2020) | ||
CARMEN | PCR | Fluorescence spectrophotometer | SHERLOCK method in one array enables more than 4,500 nucleic acids. | (Ackerman et al., 2020) | |
CARVER | PCR | Fluorescence spectrophotometer | Most advanced system to diagnose a sample using the SHERLOCK method, treat a viral infection, and measure the effectiveness of the treatment | (Freije et al., 2019) |
CARMEN, Combinatorial Arrayed Reactions for Multiplexed Evaluation of Nucleic acids; CARVER, Cas13-assisted restriction of viral expression and readout; CREST, Cas13-based, Rugged, Equitable, Scalable Testing; CRISDA, CRISPR/Cas9-triggered nicking endonuclease-mediated strand displacement amplification; CRISPR, clustered regularly interspaced short palindromic repeats; DETECTR, DNA Endonuclease Targeted CRISPR Trans Reporter; FELUDA, FNCAS9 Editor-Linked Uniform Detection Assay; HOLMES, one-HOur Low-cost Multipurpose highly Efficient System; LAMP, loop-mediated isothermal amplification; PAM, protospacer adjacent motif; RNP, ribonucleoprotein; RPA, recombinase polymerase amplification; SHERLOCK, specific high-sensitivity enzymatic reporter unlocking.