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dc.contributor.authorHernández Fernaud, Juan Ramón 
dc.contributor.authorSmits, Veronique A.J.
dc.contributor.authorHernández-Carralero, Esperanza
dc.contributor.authorPaz-Cabrera, María Cristina
dc.contributor.authorCabrera, Elisa
dc.contributor.authorHernández-Reyes, Yeray
dc.contributor.authorGillespie, David A.
dc.contributor.authorSalido, Eduardo C. 
dc.contributor.authorHernández-Porto, Miriam
dc.contributor.authorFreire, Raimundo
dc.contributor.otherBioquímica, Microbiología, Biología Celular y Genética
dc.contributor.otherUnidad de Investigación, Hospital Universitario de Canarias.
dc.date.accessioned2024-09-23T20:06:01Z
dc.date.available2024-09-23T20:06:01Z
dc.date.issued2021
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/38848
dc.descriptionDOI: 10.1016/j.bbrc.2021.01.073
dc.description.abstractmade to identify infected patients and to detect patients with a positive immune response against the virus. Currently, attemprs ro generare a vaccine against the coronavirus are ongoing. To understand SARSCoV- 2 immunoreactivity, we compared the lgG antibody response against SARS-CoV-2 in infected versus control patients by dot blot using recombinant viral particle proteins: N (Nucleocapsid ). M (Membrane) and S (Spike). In addition, we used difTerent prorein fragments of the N and S protein to map immune epitopes. Most of the COVID-19 patients presented a speci fic immune response against the full length and fragments of the N protein and. to lesser exten t. against a fragment containing amino acids 300- 685 of the S protein. In contrast, immunoreacrivity against other S protein fragments or the M prorein was low. This response is speci fic for COVID-19 patien ts as very few of the control patients displayed immunoreactiviry, like ly reflecting an immune response against other coronaviruses. Altogether. our results may help develop method(s) for measuring COVID-19 antibody response, selectivity of methods detecting such SARS-CoV-2 antibodies and vaccine development.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesBiochemical and Biophysical Research Communications 543 (2021
dc.rightsLicencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES
dc.titleThe Nucleocapsid protein triggers the main humoral immune response in COVID-19 patients
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.bbrc.2021.01.073
dc.subject.keywordNucleocapsid proteinen
dc.subject.keywordMembrane proteinen
dc.subject.keywordSpike proteinen
dc.subject.keywordSARS-CoV-2en
dc.subject.keywordCOVID-19
dc.subject.keywordlmmunotesten


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