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Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays

Background: Antibodies to microbes, or to autoantigens, are important markers of disease. Antibody detection (serology) can reveal both past and recent infections. There is a great need for development of rational ways of detecting and quantifying antibodies, both for humans and animals. Traditional...

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Autores principales: Rizwan, Muhammad, Rönnberg, Bengt, Cistjakovs, Maksims, Lundkvist, Åke, Pipkorn, Rudiger, Blomberg, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040969/
https://www.ncbi.nlm.nih.gov/pubmed/27600087
http://dx.doi.org/10.3390/microarrays5030022
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author Rizwan, Muhammad
Rönnberg, Bengt
Cistjakovs, Maksims
Lundkvist, Åke
Pipkorn, Rudiger
Blomberg, Jonas
author_facet Rizwan, Muhammad
Rönnberg, Bengt
Cistjakovs, Maksims
Lundkvist, Åke
Pipkorn, Rudiger
Blomberg, Jonas
author_sort Rizwan, Muhammad
collection PubMed
description Background: Antibodies to microbes, or to autoantigens, are important markers of disease. Antibody detection (serology) can reveal both past and recent infections. There is a great need for development of rational ways of detecting and quantifying antibodies, both for humans and animals. Traditionally, serology using synthetic antigens covers linear epitopes using up to 30 amino acid peptides. Methods: We here report that peptides of 100 amino acids or longer (“megapeptides”), designed and synthesized for optimal serological performance, can successfully be used as detection antigens in a suspension multiplex immunoassay (SMIA). Megapeptides can quickly be created just from pathogen sequences. A combination of rational sequencing and bioinformatic routines for definition of diagnostically-relevant antigens can, thus, rapidly yield efficient serological diagnostic tools for an emerging infectious pathogen. Results: We designed megapeptides using bioinformatics and viral genome sequences. These long peptides were tested as antigens for the presence of antibodies in human serum to the filo-, herpes-, and polyoma virus families in a multiplex microarray system. All of these virus families contain recently discovered or emerging infectious viruses. Conclusion: Long synthetic peptides can be useful as serological diagnostic antigens, serving as biomarkers, in suspension microarrays.
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spelling pubmed-50409692016-10-05 Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays Rizwan, Muhammad Rönnberg, Bengt Cistjakovs, Maksims Lundkvist, Åke Pipkorn, Rudiger Blomberg, Jonas Microarrays (Basel) Article Background: Antibodies to microbes, or to autoantigens, are important markers of disease. Antibody detection (serology) can reveal both past and recent infections. There is a great need for development of rational ways of detecting and quantifying antibodies, both for humans and animals. Traditionally, serology using synthetic antigens covers linear epitopes using up to 30 amino acid peptides. Methods: We here report that peptides of 100 amino acids or longer (“megapeptides”), designed and synthesized for optimal serological performance, can successfully be used as detection antigens in a suspension multiplex immunoassay (SMIA). Megapeptides can quickly be created just from pathogen sequences. A combination of rational sequencing and bioinformatic routines for definition of diagnostically-relevant antigens can, thus, rapidly yield efficient serological diagnostic tools for an emerging infectious pathogen. Results: We designed megapeptides using bioinformatics and viral genome sequences. These long peptides were tested as antigens for the presence of antibodies in human serum to the filo-, herpes-, and polyoma virus families in a multiplex microarray system. All of these virus families contain recently discovered or emerging infectious viruses. Conclusion: Long synthetic peptides can be useful as serological diagnostic antigens, serving as biomarkers, in suspension microarrays. MDPI 2016-08-10 /pmc/articles/PMC5040969/ /pubmed/27600087 http://dx.doi.org/10.3390/microarrays5030022 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rizwan, Muhammad
Rönnberg, Bengt
Cistjakovs, Maksims
Lundkvist, Åke
Pipkorn, Rudiger
Blomberg, Jonas
Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays
title Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays
title_full Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays
title_fullStr Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays
title_full_unstemmed Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays
title_short Serology in the Digital Age: Using Long Synthetic Peptides Created from Nucleic Acid Sequences as Antigens in Microarrays
title_sort serology in the digital age: using long synthetic peptides created from nucleic acid sequences as antigens in microarrays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040969/
https://www.ncbi.nlm.nih.gov/pubmed/27600087
http://dx.doi.org/10.3390/microarrays5030022
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