L. Morais, A. Argondizzo, Dílson Silva, S. Missailidis
{"title":"Aptamers against the Zika virus NS1 protein, for a serological diagnostic assay development","authors":"L. Morais, A. Argondizzo, Dílson Silva, S. Missailidis","doi":"10.1063/1.5138061","DOIUrl":null,"url":null,"abstract":"Zika virus (ZIKV) belongs to the Flaviviridae family and its recent outbreak and association with human diseases (e.g. neurological disorders and microcephaly in babies) have raised global health concerns. Its differentiation from Dengue in accurate diagnostic assays are of great importance. The viral NS1 protein is a secreted protein and can be an ideal target for diagnostic assay development. We have thus selected NS1 as target for aptamer selection and study. Single-stranded DNA oligonucleotides aptamers have been previously selected for this target, and here we present the study of such aptamers by fluorescent spectroscopy, CD and ELISA in order to characterize their interaction and select the best candidate for further future assay development.Zika virus (ZIKV) belongs to the Flaviviridae family and its recent outbreak and association with human diseases (e.g. neurological disorders and microcephaly in babies) have raised global health concerns. Its differentiation from Dengue in accurate diagnostic assays are of great importance. The viral NS1 protein is a secreted protein and can be an ideal target for diagnostic assay development. We have thus selected NS1 as target for aptamer selection and study. Single-stranded DNA oligonucleotides aptamers have been previously selected for this target, and here we present the study of such aptamers by fluorescent spectroscopy, CD and ELISA in order to characterize their interaction and select the best candidate for further future assay development.","PeriodicalId":20565,"journal":{"name":"PROCEEDINGS OF THE INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2019 (ICCMSE-2019)","volume":"46 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PROCEEDINGS OF THE INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2019 (ICCMSE-2019)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1063/1.5138061","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Zika virus (ZIKV) belongs to the Flaviviridae family and its recent outbreak and association with human diseases (e.g. neurological disorders and microcephaly in babies) have raised global health concerns. Its differentiation from Dengue in accurate diagnostic assays are of great importance. The viral NS1 protein is a secreted protein and can be an ideal target for diagnostic assay development. We have thus selected NS1 as target for aptamer selection and study. Single-stranded DNA oligonucleotides aptamers have been previously selected for this target, and here we present the study of such aptamers by fluorescent spectroscopy, CD and ELISA in order to characterize their interaction and select the best candidate for further future assay development.Zika virus (ZIKV) belongs to the Flaviviridae family and its recent outbreak and association with human diseases (e.g. neurological disorders and microcephaly in babies) have raised global health concerns. Its differentiation from Dengue in accurate diagnostic assays are of great importance. The viral NS1 protein is a secreted protein and can be an ideal target for diagnostic assay development. We have thus selected NS1 as target for aptamer selection and study. Single-stranded DNA oligonucleotides aptamers have been previously selected for this target, and here we present the study of such aptamers by fluorescent spectroscopy, CD and ELISA in order to characterize their interaction and select the best candidate for further future assay development.