Abstract
Recently, there has been a rapid progress in the development of techniques for isothermal amplification of nucleic acids as an alternative to polymerase chain reaction (PCR). The advantage of these methods is that the nucleic acids amplification can be carried out at constant temperature, unlike PCR, which requires cyclic temperature changes. Moreover, isothermal amplification can be conducted directly in living cells. This review describes the principles of isothermal amplification techniques and demonstrates their high efficiency in designing new highly sensitive detection methods of nucleic acids and enzymes involved in their modifications. The data on successful application of isothermal amplification methods for the analysis of cells and biomolecules with the use of DNA/RNA aptamers are presented.
Keywords: nucleic acids, amplification, isothermal, bioanalysis, aptamers
Abbreviations
- CHA
catalytic hairpin assembly
- EASA
exonu-clease Ill-assisted signal amplification
- EXPAR
exponential amplification reaction
- HCR
hybridization chain reaction
- HDA
helicase-dependent amplification
- ICSDP
isothermal circular strand displacement polymerization
- LAMP
loop-mediated isothermal amplification
- MDA
multiple displacement amplification
- NASBA
nucleic acid sequence-based amplification
- pWGA
primase-based whole genome amplification
- RCA
rolling circle amplification
- RPA
recombinase polymerase amplification
- SDA
strand-displacement amplification
- WGA
whole genome amplification
Funding
This work was supported by the Russian Science Foundation (grant 17-14-01042).
Ethical approval
This article does not contain studies with human participants or animals performed by any of the authors.
Footnotes
Russian Text © The Author(s), 2020, published in Biokhimiya, 2020, Vol. 85, No. 2, pp. 174–196.
Conflict of interest
The authors declare no conflict of interest in financial or any other sphere.
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