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Rapid high-throughput compatible label-free virus particle quantification method based on time-resolved luminescence.
Kopra, Kari; Hassan, Nazia; Vuorinen, Emmiliisa; Valtonen, Salla; Mahran, Randa; Habib, Huda; Jalkanen, Pinja; Susi, Petri; Hytönen, Vesa; Hankaniemi, Minna; Ylä-Herttuala, Seppo; Kakkola, Laura; Peurla, Markus; Härmä, Harri.
Afiliação
  • Kopra K; Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.
  • Hassan N; Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.
  • Vuorinen E; Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.
  • Valtonen S; Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.
  • Mahran R; Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.
  • Habib H; Department of Chemistry, University of Turku, Henrikinkatu 2, 20500, Turku, Finland.
  • Jalkanen P; Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Susi P; Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Hytönen V; Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Hankaniemi M; Faculty of Medicine and Health Technology, Tampere University, 33014, Tampere, Finland.
  • Ylä-Herttuala S; Faculty of Medicine and Health Technology, Tampere University, 33014, Tampere, Finland.
  • Kakkola L; A.I.Virtanen Institute, University of Eastern Finland and Gene Therapy Unit, Kuopio University Hospital, 70210, Kuopio, Finland.
  • Peurla M; Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
  • Härmä H; Institute of Biomedicine, University of Turku, Kiinamyllynkatu 10, 20520, Turku, Finland.
Anal Bioanal Chem ; 414(15): 4509-4518, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35581427
ABSTRACT
Viruses play a major role in modern society and create risks from global pandemics and bioterrorism to challenges in agriculture. Virus infectivity assays and genome copy number determination methods are often used to obtain information on virus preparations used in diagnostics and vaccine development. However, these methods do not provide information on virus particle count. Current methods to measure the number of viral particles are often cumbersome and require highly purified virus preparations and expensive instrumentation. To tackle these problems, we developed a simple and cost-effective time-resolved luminescence-based method for virus particle quantification. This mix-and-measure technique is based on the recognition of the virus particles by an external Eu3+-peptide probe, providing results on virus count in minutes. The method enables the detection of non-enveloped and enveloped viruses, having over tenfold higher detectability for enveloped, dynamic range from 5E6 to 3E10 vp/mL, than non-enveloped viruses. Multiple non-enveloped and enveloped viruses were used to demonstrate the functionality and robustness of the Protein-Probe method.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus / Viroses Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus / Viroses Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article