Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles

Abstract Advancements in understanding and engineering of virus-based nanomaterials (VBNs) for biomedical applications motivate a need to explore the interfaces between VBNs and other biomedically-relevant chemistries and materials. While several strategies have been used to investigate some of thes...

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Main Authors: Matthew J. McNulty, Naomi Hamada, Jesse Delzio, Liber McKee, Somen Nandi, Marjorie L. Longo, Karen A. McDonald
Format: Article
Language:English
Published: BMC 2022-03-01
Series:Journal of Nanobiotechnology
Subjects:
Online Access:https://doi.org/10.1186/s12951-022-01303-1
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author Matthew J. McNulty
Naomi Hamada
Jesse Delzio
Liber McKee
Somen Nandi
Marjorie L. Longo
Karen A. McDonald
author_facet Matthew J. McNulty
Naomi Hamada
Jesse Delzio
Liber McKee
Somen Nandi
Marjorie L. Longo
Karen A. McDonald
author_sort Matthew J. McNulty
collection DOAJ
description Abstract Advancements in understanding and engineering of virus-based nanomaterials (VBNs) for biomedical applications motivate a need to explore the interfaces between VBNs and other biomedically-relevant chemistries and materials. While several strategies have been used to investigate some of these interfaces with promising initial results, including VBN-containing slow-release implants and VBN-activated bioceramic bone scaffolds, there remains a need to establish VBN-immobilized three dimensional materials that exhibit improved stability and diffusion characteristics for biosensing and other analyte-capture applications. Silica sol–gel chemistries have been researched for biomedical applications over several decades and are well understood; various cellular organisms and biomolecules (e.g., bacteria, algae, enzymes) have been immobilized in silica sol-gels to improve viability, activity, and form factor (i.e., ease of use). Here we present the immobilization of an antibody-binding VBN in silica sol–gel by pore confinement. We have shown that the resulting system is sufficiently diffuse to allow antibodies to migrate in and out of the matrix. We also show that the immobilized VBN is capable of antibody binding and elution functionality under different buffer conditions for multiple use cycles. The promising results of the VBN and silica sol–gel interface indicate a general applicability for VBN-based bioseparations and biosensing applications. Graphical Abstract
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spelling doaj.art-2fd64c3d75bf483b95ec3df163ac40032022-12-22T03:58:37ZengBMCJournal of Nanobiotechnology1477-31552022-03-012011910.1186/s12951-022-01303-1Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticlesMatthew J. McNulty0Naomi Hamada1Jesse Delzio2Liber McKee3Somen Nandi4Marjorie L. Longo5Karen A. McDonald6Department of Chemical Engineering, University of California DavisDepartment of Chemical Engineering, University of California DavisDepartment of Chemical Engineering, University of California DavisDepartment of Chemical Engineering, University of California DavisDepartment of Chemical Engineering, University of California DavisDepartment of Chemical Engineering, University of California DavisDepartment of Chemical Engineering, University of California DavisAbstract Advancements in understanding and engineering of virus-based nanomaterials (VBNs) for biomedical applications motivate a need to explore the interfaces between VBNs and other biomedically-relevant chemistries and materials. While several strategies have been used to investigate some of these interfaces with promising initial results, including VBN-containing slow-release implants and VBN-activated bioceramic bone scaffolds, there remains a need to establish VBN-immobilized three dimensional materials that exhibit improved stability and diffusion characteristics for biosensing and other analyte-capture applications. Silica sol–gel chemistries have been researched for biomedical applications over several decades and are well understood; various cellular organisms and biomolecules (e.g., bacteria, algae, enzymes) have been immobilized in silica sol-gels to improve viability, activity, and form factor (i.e., ease of use). Here we present the immobilization of an antibody-binding VBN in silica sol–gel by pore confinement. We have shown that the resulting system is sufficiently diffuse to allow antibodies to migrate in and out of the matrix. We also show that the immobilized VBN is capable of antibody binding and elution functionality under different buffer conditions for multiple use cycles. The promising results of the VBN and silica sol–gel interface indicate a general applicability for VBN-based bioseparations and biosensing applications. Graphical Abstracthttps://doi.org/10.1186/s12951-022-01303-1Virus-based nanomaterialMolecular pharmingNanobiotechnologyTobamovirusPlant-made pharmaceuticalsSilica sol–gel
spellingShingle Matthew J. McNulty
Naomi Hamada
Jesse Delzio
Liber McKee
Somen Nandi
Marjorie L. Longo
Karen A. McDonald
Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles
Journal of Nanobiotechnology
Virus-based nanomaterial
Molecular pharming
Nanobiotechnology
Tobamovirus
Plant-made pharmaceuticals
Silica sol–gel
title Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles
title_full Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles
title_fullStr Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles
title_full_unstemmed Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles
title_short Functionalizing silica sol–gel with entrapped plant virus-based immunosorbent nanoparticles
title_sort functionalizing silica sol gel with entrapped plant virus based immunosorbent nanoparticles
topic Virus-based nanomaterial
Molecular pharming
Nanobiotechnology
Tobamovirus
Plant-made pharmaceuticals
Silica sol–gel
url https://doi.org/10.1186/s12951-022-01303-1
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