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Reverse Transcription Polymerase Chain Reaction in Giant Unilamellar Vesicles.
Tsugane, Mamiko; Suzuki, Hiroaki.
Afiliación
  • Tsugane M; Department of Precision Mechanics, Faculty of Science and Engineering, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, Tokyo, Japan.
  • Suzuki H; Japan Society for the Promotion of Science (JSPS), 5-3-1 Kojimachi, Chiyoda-ku, Tokyo, Japan.
Sci Rep ; 8(1): 9214, 2018 06 15.
Article en En | MEDLINE | ID: mdl-29907779
ABSTRACT
We assessed the applicability of giant unilamellar vesicles (GUVs) for RNA detection using in vesicle reverse transcription polymerase chain reaction (RT-PCR). We prepared GUVs that encapsulated one-pot RT-PCR reaction mixture including template RNA, primers, and Taqman probe, using water-in-oil emulsion transfer method. After thermal cycling, we analysed the GUVs that exhibited intense fluorescence signals, which represented the cDNA amplification. The detailed analysis of flow cytometry data demonstrated that rRNA and mRNA in the total RNA can be amplified from 10-100 copies in the GUVs with 5-10 µm diameter, although the fraction of reactable GUV was approximately 60% at most. Moreover, we report that the target RNA, which was directly transferred into the GUV reactors via membrane fusion, can be amplified and detected using in vesicle RT-PCR. These results suggest that the GUVs can be used as biomimetic reactors capable of performing PCR and RT-PCR, which are important in analytical and diagnostic applications with additional functions.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN Mensajero / ARN Ribosómico / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Liposomas Unilamelares / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN Mensajero / ARN Ribosómico / Reacción en Cadena de la Polimerasa de Transcriptasa Inversa / Liposomas Unilamelares / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article