Multiplexed detection of viral antigen and RNA using nanopore sensing and encoded molecular probes.
Multiplexed detection of viral antigen and RNA using nanopore sensing and encoded molecular probes.
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DOI:
10.1038/s41467-023-43004-9
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发表时间:
2023-11-14
影响因子:
16.6
通讯作者:
Edel, Joshua B.
中科院分区:
文献类型:
--
作者:
Ren, Ren;Cai, Shenglin;Fang, Xiaona;Wang, Xiaoyi;Zhang, Zheng;Damiani, Micol;Hudlerova, Charlotte;Rosa, Annachiara;Hope, Joshua;Cook, Nicola J.;Gorelkin, Peter;Erofeev, Alexander;Novak, Pavel;Badhan, Anjna;Crone, Michael;Freemont, Paul;Taylor, Graham P.;Tang, Longhua;Edwards, Christopher;Shevchuk, Andrew;Cherepanov, Peter;Luo, Zhaofeng;Tan, Weihong;Korchev, Yuri;Ivanov, Aleksandar P.;Edel, Joshua B.
We report on single-molecule nanopore sensing combined with position-encoded DNA molecular probes, with chemistry tuned to simultaneously identify various antigen proteins and multiple RNA gene fragments of SARS-CoV-2 with high sensitivity and selectivity. We show that this sensing strategy can directly detect spike (S) and nucleocapsid (N) proteins in unprocessed human saliva. Moreover, our approach enables the identification of RNA fragments from patient samples using nasal/throat swabs, enabling the identification of critical mutations such as D614G, G446S, or Y144del among viral variants. In particular, it can detect and discriminate between SARS-CoV-2 lineages of wild-type B.1.1.7 (Alpha), B.1.617.2 (Delta), and B.1.1.539 (Omicron) within a single measurement without the need for nucleic acid sequencing. The sensing strategy of the molecular probes is easily adaptable to other viral targets and diseases and can be expanded depending on the application required. Fast discrimination of SARS-CoV-2 variants in clinical samples remains a challenge. Here, authors report on single molecule nanopore sensing combined with DNA molecular probes to simultaneously detect various antigens and RNA mutations of SARS-CoV-2 variants in patient samples.
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影响因子:
16.6
作者:
Cai S;Pataillot-Meakin T;Shibakawa A;Ren R;Bevan CL;Ladame S;Ivanov AP;Edel JB
通讯作者:
Edel JB
影响因子:
16.6
作者:
Freedman KJ;Otto LM;Ivanov AP;Barik A;Oh SH;Edel JB
通讯作者:
Edel JB
影响因子:
1.7
作者:
Ochola L;Ogongo P;Mungai S;Gitaka J;Suliman S
通讯作者:
Suliman S
影响因子:
9.4
作者:
Lee RA;Herigon JC;Benedetti A;Pollock NR;Denkinger CM
通讯作者:
Denkinger CM
DOI:
10.1056/nejmoa2119451
发表时间:
2022-04-21
期刊:
The New England journal of medicine
影响因子:
--
作者:
Andrews N;Stowe J;Kirsebom F;Toffa S;Rickeard T;Gallagher E;Gower C;Kall M;Groves N;O'Connell AM;Simons D;Blomquist PB;Zaidi A;Nash S;Iwani Binti Abdul Aziz N;Thelwall S;Dabrera G;Myers R;Amirthalingam G;Gharbia S;Barrett JC;Elson R;Ladhani SN;Ferguson N;Zambon M;Campbell CNJ;Brown K;Hopkins S;Chand M;Ramsay M;Lopez Bernal J
通讯作者:
Lopez Bernal J