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Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants

Virus recognition has been driven to the forefront of molecular recognition research due to the COVID‐19 pandemic. Development of highly sensitive recognition elements, both natural and synthetic is critical to facing such a global issue. However, as viruses mutate, it is possible for their recognit...

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Autores principales: Sullivan, Mark V., Allabush, Francia, Flynn, Harriet, Balansethupathy, Banushan, Reed, Joseph A., Barnes, Edward T., Robson, Callum, O'Hara, Phoebe, Milburn, Laura J., Bunka, David, Tolley, Arron, Mendes, Paula M., Tucker, James H. R., Turner, Nicholas W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242533/
https://www.ncbi.nlm.nih.gov/pubmed/37287590
http://dx.doi.org/10.1002/gch2.202200215
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author Sullivan, Mark V.
Allabush, Francia
Flynn, Harriet
Balansethupathy, Banushan
Reed, Joseph A.
Barnes, Edward T.
Robson, Callum
O'Hara, Phoebe
Milburn, Laura J.
Bunka, David
Tolley, Arron
Mendes, Paula M.
Tucker, James H. R.
Turner, Nicholas W.
author_facet Sullivan, Mark V.
Allabush, Francia
Flynn, Harriet
Balansethupathy, Banushan
Reed, Joseph A.
Barnes, Edward T.
Robson, Callum
O'Hara, Phoebe
Milburn, Laura J.
Bunka, David
Tolley, Arron
Mendes, Paula M.
Tucker, James H. R.
Turner, Nicholas W.
author_sort Sullivan, Mark V.
collection PubMed
description Virus recognition has been driven to the forefront of molecular recognition research due to the COVID‐19 pandemic. Development of highly sensitive recognition elements, both natural and synthetic is critical to facing such a global issue. However, as viruses mutate, it is possible for their recognition to wane through changes in the target substrate, which can lead to detection avoidance and increased false negatives. Likewise, the ability to detect specific variants is of great interest for clinical analysis of all viruses. Here, a hybrid aptamer‐molecularly imprinted polymer (aptaMIP), that maintains selective recognition for the spike protein template across various mutations, while improving performance over individual aptamer or MIP components (which themselves demonstrate excellent performance). The aptaMIP exhibits an equilibrium dissociation constant of 1.61 nM toward its template which matches or exceeds published examples of imprinting of the spike protein. The work here demonstrates that “fixing” the aptamer within a polymeric scaffold increases its capability to selectivity recognize its original target and points toward a methodology that will allow variant selective molecular recognition with exceptional affinity.
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spelling pubmed-102425332023-06-07 Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants Sullivan, Mark V. Allabush, Francia Flynn, Harriet Balansethupathy, Banushan Reed, Joseph A. Barnes, Edward T. Robson, Callum O'Hara, Phoebe Milburn, Laura J. Bunka, David Tolley, Arron Mendes, Paula M. Tucker, James H. R. Turner, Nicholas W. Glob Chall Research Articles Virus recognition has been driven to the forefront of molecular recognition research due to the COVID‐19 pandemic. Development of highly sensitive recognition elements, both natural and synthetic is critical to facing such a global issue. However, as viruses mutate, it is possible for their recognition to wane through changes in the target substrate, which can lead to detection avoidance and increased false negatives. Likewise, the ability to detect specific variants is of great interest for clinical analysis of all viruses. Here, a hybrid aptamer‐molecularly imprinted polymer (aptaMIP), that maintains selective recognition for the spike protein template across various mutations, while improving performance over individual aptamer or MIP components (which themselves demonstrate excellent performance). The aptaMIP exhibits an equilibrium dissociation constant of 1.61 nM toward its template which matches or exceeds published examples of imprinting of the spike protein. The work here demonstrates that “fixing” the aptamer within a polymeric scaffold increases its capability to selectivity recognize its original target and points toward a methodology that will allow variant selective molecular recognition with exceptional affinity. John Wiley and Sons Inc. 2023-03-20 /pmc/articles/PMC10242533/ /pubmed/37287590 http://dx.doi.org/10.1002/gch2.202200215 Text en © 2023 The Authors. Global Challenges published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sullivan, Mark V.
Allabush, Francia
Flynn, Harriet
Balansethupathy, Banushan
Reed, Joseph A.
Barnes, Edward T.
Robson, Callum
O'Hara, Phoebe
Milburn, Laura J.
Bunka, David
Tolley, Arron
Mendes, Paula M.
Tucker, James H. R.
Turner, Nicholas W.
Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants
title Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants
title_full Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants
title_fullStr Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants
title_full_unstemmed Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants
title_short Highly Selective Aptamer‐Molecularly Imprinted Polymer Hybrids for Recognition of SARS‐CoV‐2 Spike Protein Variants
title_sort highly selective aptamer‐molecularly imprinted polymer hybrids for recognition of sars‐cov‐2 spike protein variants
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242533/
https://www.ncbi.nlm.nih.gov/pubmed/37287590
http://dx.doi.org/10.1002/gch2.202200215
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