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Ultrasensitive detection of proteins and sugars at single-cell level

Each cell produces its own responses even if it appears identical to other cells. To analyze these individual cell characteristics, we need to measure trace amounts of molecules in a single cell. Nucleic acids in a single cell can be easily amplified by polymerase chain reaction, but single-cell mea...

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Detalles Bibliográficos
Autores principales: Watabe, Satoshi, Morikawa, Mika, Kaneda, Mugiho, Nakaishi, Kazunari, Nakatsuma, Akira, Ninomiya, Masaki, Yoshimura, Teruki, Miura, Toshiaki, Ito, Etsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4802808/
https://www.ncbi.nlm.nih.gov/pubmed/27064305
http://dx.doi.org/10.1080/19420889.2015.1124201
Descripción
Sumario:Each cell produces its own responses even if it appears identical to other cells. To analyze these individual cell characteristics, we need to measure trace amounts of molecules in a single cell. Nucleic acids in a single cell can be easily amplified by polymerase chain reaction, but single-cell measurement of proteins and sugars will require de novo techniques. In the present study, we outline the techniques we have developed toward this end. For proteins, our ultrasensitive enzyme-linked immunosorbent assay (ELISA) coupled with thionicotinamide-adenine dinucleotide cycling can detect proteins at subattomoles per assay. For sugars, fluorescence correlation spectroscopy coupled with glucose oxidase-catalyzed reaction allows us to measure glucose at tens of nM. Our methods thus offer versatile techniques for single-cell-level analyses, and they are hoped to strongly promote single-cell biology as well as to develop noninvasive tests in clinical medicine.