Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity

Deployment of the elongated flexuous virions of Turnip mosaic virus (TuMV), a potyvirus, for peptide display on their external surface has been previously reported by us. Nonetheless, both in TuMV and other potyviruses some peptides hinder the ability of the virus to infect host plants. We found that a peptide derived from the human thrombin receptor (TR) inhibited TuMV infectivity. In an effort to get around this problem, TuMV virus-like particles (VLPs) were produced in plants by transient high-level expression of wild-type or recombinant coat protein (CP). Significant production of both recombinant and non-recombinant CP proteins was obtained from plant leaves. Assembled particles of each of these two proteins into VLPs were observed under the electron microscope. The capacity of TR-CP VLPs to log-increase the ability of TR antibody-sensing was confirmed. These results confirm that the use of VLPs is an effective way to overcome the problem of displaying infectivity-interfering peptides. This is yet another way of exploiting the use of plant-made flexuous elongated VLPs for nanobiotechnological purposes. © 2017 Elsevier B.V.

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Bibliographic Details
Main Authors: González-Gamboa, I., Manrique, P., Sánchez, F., Ponz Ascaso, Fernando
Format: artículo biblioteca
Language:English
Published: Elsevier 2017
Subjects:Viral nanoparticles, Peptide presentation, Thrombin receptor peptide, Antibody sensing, Virus-like particles,
Online Access:http://hdl.handle.net/20.500.12792/1942
http://hdl.handle.net/10261/292054
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spelling dig-inia-es-10261-2920542023-02-20T07:25:06Z Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity González-Gamboa, I. Manrique, P. Sánchez, F. Ponz Ascaso, Fernando Viral nanoparticles Peptide presentation Thrombin receptor peptide Antibody sensing Virus-like particles Deployment of the elongated flexuous virions of Turnip mosaic virus (TuMV), a potyvirus, for peptide display on their external surface has been previously reported by us. Nonetheless, both in TuMV and other potyviruses some peptides hinder the ability of the virus to infect host plants. We found that a peptide derived from the human thrombin receptor (TR) inhibited TuMV infectivity. In an effort to get around this problem, TuMV virus-like particles (VLPs) were produced in plants by transient high-level expression of wild-type or recombinant coat protein (CP). Significant production of both recombinant and non-recombinant CP proteins was obtained from plant leaves. Assembled particles of each of these two proteins into VLPs were observed under the electron microscope. The capacity of TR-CP VLPs to log-increase the ability of TR antibody-sensing was confirmed. These results confirm that the use of VLPs is an effective way to overcome the problem of displaying infectivity-interfering peptides. This is yet another way of exploiting the use of plant-made flexuous elongated VLPs for nanobiotechnological purposes. © 2017 Elsevier B.V. 2023-02-20T07:25:06Z 2023-02-20T07:25:06Z 2017 artículo Journal of Biotechnology 254: 17-24 (2017) 0168-1656 http://hdl.handle.net/20.500.12792/1942 http://hdl.handle.net/10261/292054 10.1016/j.jbiotec.2017.06.014 en none Elsevier
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Viral nanoparticles
Peptide presentation
Thrombin receptor peptide
Antibody sensing
Virus-like particles
Viral nanoparticles
Peptide presentation
Thrombin receptor peptide
Antibody sensing
Virus-like particles
spellingShingle Viral nanoparticles
Peptide presentation
Thrombin receptor peptide
Antibody sensing
Virus-like particles
Viral nanoparticles
Peptide presentation
Thrombin receptor peptide
Antibody sensing
Virus-like particles
González-Gamboa, I.
Manrique, P.
Sánchez, F.
Ponz Ascaso, Fernando
Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
description Deployment of the elongated flexuous virions of Turnip mosaic virus (TuMV), a potyvirus, for peptide display on their external surface has been previously reported by us. Nonetheless, both in TuMV and other potyviruses some peptides hinder the ability of the virus to infect host plants. We found that a peptide derived from the human thrombin receptor (TR) inhibited TuMV infectivity. In an effort to get around this problem, TuMV virus-like particles (VLPs) were produced in plants by transient high-level expression of wild-type or recombinant coat protein (CP). Significant production of both recombinant and non-recombinant CP proteins was obtained from plant leaves. Assembled particles of each of these two proteins into VLPs were observed under the electron microscope. The capacity of TR-CP VLPs to log-increase the ability of TR antibody-sensing was confirmed. These results confirm that the use of VLPs is an effective way to overcome the problem of displaying infectivity-interfering peptides. This is yet another way of exploiting the use of plant-made flexuous elongated VLPs for nanobiotechnological purposes. © 2017 Elsevier B.V.
format artículo
topic_facet Viral nanoparticles
Peptide presentation
Thrombin receptor peptide
Antibody sensing
Virus-like particles
author González-Gamboa, I.
Manrique, P.
Sánchez, F.
Ponz Ascaso, Fernando
author_facet González-Gamboa, I.
Manrique, P.
Sánchez, F.
Ponz Ascaso, Fernando
author_sort González-Gamboa, I.
title Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
title_short Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
title_full Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
title_fullStr Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
title_full_unstemmed Plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
title_sort plant-made potyvirus-like particles used for log-increasing antibody sensing capacity
publisher Elsevier
publishDate 2017
url http://hdl.handle.net/20.500.12792/1942
http://hdl.handle.net/10261/292054
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