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PMCA for ultrasensitive detection of prions and to study disease biology

The emergence of a novel class of infectious agent composed exclusively of a misfolded protein (termed prions) has been a challenge in modern biomedicine. Despite similarities on the behavior of prions with respect to conventional pathogens, the many uncertainties regarding the biology and virulence...

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Detalles Bibliográficos
Autores principales: Wang, Fei, Pritzkow, Sandra, Soto, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790818/
https://www.ncbi.nlm.nih.gov/pubmed/36567368
http://dx.doi.org/10.1007/s00441-022-03727-5
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author Wang, Fei
Pritzkow, Sandra
Soto, Claudio
author_facet Wang, Fei
Pritzkow, Sandra
Soto, Claudio
author_sort Wang, Fei
collection PubMed
description The emergence of a novel class of infectious agent composed exclusively of a misfolded protein (termed prions) has been a challenge in modern biomedicine. Despite similarities on the behavior of prions with respect to conventional pathogens, the many uncertainties regarding the biology and virulence of prions make them a worrisome paradigm. Since prions do not contain nucleic acids and rely on a very different way of replication and spreading, it was necessary to invent a novel technology to study them. In this article, we provide an overview of such a technology, termed protein misfolding cyclic amplification (PMCA), and summarize its many applications to detect prions and understand prion biology.
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spelling pubmed-97908182022-12-27 PMCA for ultrasensitive detection of prions and to study disease biology Wang, Fei Pritzkow, Sandra Soto, Claudio Cell Tissue Res Review The emergence of a novel class of infectious agent composed exclusively of a misfolded protein (termed prions) has been a challenge in modern biomedicine. Despite similarities on the behavior of prions with respect to conventional pathogens, the many uncertainties regarding the biology and virulence of prions make them a worrisome paradigm. Since prions do not contain nucleic acids and rely on a very different way of replication and spreading, it was necessary to invent a novel technology to study them. In this article, we provide an overview of such a technology, termed protein misfolding cyclic amplification (PMCA), and summarize its many applications to detect prions and understand prion biology. Springer Berlin Heidelberg 2022-12-26 2023 /pmc/articles/PMC9790818/ /pubmed/36567368 http://dx.doi.org/10.1007/s00441-022-03727-5 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Wang, Fei
Pritzkow, Sandra
Soto, Claudio
PMCA for ultrasensitive detection of prions and to study disease biology
title PMCA for ultrasensitive detection of prions and to study disease biology
title_full PMCA for ultrasensitive detection of prions and to study disease biology
title_fullStr PMCA for ultrasensitive detection of prions and to study disease biology
title_full_unstemmed PMCA for ultrasensitive detection of prions and to study disease biology
title_short PMCA for ultrasensitive detection of prions and to study disease biology
title_sort pmca for ultrasensitive detection of prions and to study disease biology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790818/
https://www.ncbi.nlm.nih.gov/pubmed/36567368
http://dx.doi.org/10.1007/s00441-022-03727-5
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