Robust Sequence Design Space for the Isothermal Exponential Amplification of Short Oligonucleotides
Source abstract
Abstract
Abstract Advances in isothermal amplification techniques have accelerated development in biosensing applications and the design of complex molecular devices. The exponential amplification reaction technique, or EXPAR, is uniquely positioned to process molecular information from short oligonucleotide strands (≈10 nucleotides length) typically encountered in molecular computing or microRNA detection. Despite its conceptual simplicity (requiring only a template strand and two enzymes), the issue of nonspecific background amplification has hindered broader adoption. In this work, a new system configuration is established at 37 °C to achieve significantly improved performance. Critical sequence motifs responsible for the excellent signal‐to‐background profile are identified and generalized as a universal adapter design framework. Orthogonal template sequences generated from the framework are implemented for a triplex reaction and successfully evaluated mixtures of multiple‐target inputs in a single‐step, one‐pot format without the need for exogenous agents.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Biosensors and Analytical Detection · Advanced Biosensing Techniques and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical & Biomolecular Engineering National University of Singapore Singapore 117585 Singapore
References (37)
Show source-provided references
1. 10.1080/10409238.2021.193792710.1080/10409238.2021.1937927 ↗
2. 10.1371/journal.pbio.004020410.1371/journal.pbio.0040204 ↗
3. 10.1371/journal.pone.023521610.1371/journal.pone.0235216 ↗
4. 10.3390/cells1008193110.3390/cells10081931 ↗
5. 10.1093/bioinformatics/bty70110.1093/bioinformatics/bty701 ↗
6. 10.1038/nchem.287210.1038/nchem.2872 ↗
7. 10.1038/s41565-019-0544-510.1038/s41565-019-0544-5 ↗
8. 10.1073/pnas.073081110010.1073/pnas.0730811100 ↗
9. 10.1021/acs.chemrev.5b0042810.1021/acs.chemrev.5b00428 ↗
10. 10.1002/anie.20171221710.1002/anie.201712217 ↗
11. 10.1073/pnas.210034711810.1073/pnas.2100347118 ↗
12. 10.1016/j.bios.2022.11468310.1016/j.bios.2022.114683 ↗
13. 10.1039/C7AN02037F10.1039/C7AN02037F ↗
14. 10.1021/acs.analchem.8b0278810.1021/acs.analchem.8b02788 ↗
15. 10.1016/j.snr.2021.10003310.1016/j.snr.2021.100033 ↗
16. 10.1038/srep3783710.1038/srep37837 ↗
17. 10.1016/j.snb.2022.13296010.1016/j.snb.2022.132960 ↗
18. 10.1016/j.microc.2023.10886610.1016/j.microc.2023.108866 ↗
19. 10.1093/nar/gkw50410.1093/nar/gkw504 ↗
20. 10.1021/acs.biochem.9b0006310.1021/acs.biochem.9b00063 ↗
21. 10.1038/ncomms1347410.1038/ncomms13474 ↗
22. 10.1021/acssensors.0c0059310.1021/acssensors.0c00593 ↗
23. 10.1126/sciadv.aay595210.1126/sciadv.aay5952 ↗
24. 10.1016/j.ymeth.2014.01.01510.1016/j.ymeth.2014.01.015 ↗
25. 10.1007/s00354-020-00089-w10.1007/s00354-020-00089-w ↗
26. 10.1038/s41586-022-05218-710.1038/s41586-022-05218-7 ↗
27. 10.1021/acssynbio.3c0038510.1021/acssynbio.3c00385 ↗
28. 10.1093/nar/gks23010.1093/nar/gks230 ↗
29. 10.1002/jcc.2159610.1002/jcc.21596 ↗
30. 10.1021/bi800746p10.1021/bi800746p ↗
31. 10.1002/bip.2234710.1002/bip.22347 ↗
32. 10.1021/ja402397810.1021/ja4023978 ↗
33. 10.1021/acsnano.3c1143510.1021/acsnano.3c11435 ↗
34. 10.1021/bi026566c10.1021/bi026566c ↗
35. 10.1021/cr800530b10.1021/cr800530b ↗
36. 10.1093/abbs/gmq08210.1093/abbs/gmq082 ↗
37. 10.1021/acs.analchem.2c0194510.1021/acs.analchem.2c01945 ↗