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  Monitoring mRNA Translation in Neuronal Processes Using Fluorescent Non-Canonical Amino Acid Tagging

Kos, A., Wanke, K., Gioio, A., Martens, G. J., Kaplan, B. B., & Aschrafi, A. (2016). Monitoring mRNA Translation in Neuronal Processes Using Fluorescent Non-Canonical Amino Acid Tagging. Journal of Histochemistry and Cytochemistry, 64(5), 323-333. doi:10.1369/0022155416641604.

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Kos_etal_monitoring_2016.pdf (Publisher version), 932KB
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Kos, Aron1, 2, Author
Wanke, Kai3, 4, 5, Author           
Gioio, Anthony, Author
Martens, Gerard J, Author
Kaplan, Barry B., Author
Aschrafi, Armaz6, Author
Affiliations:
1Donders Institute for Brain, Cognition and Behaviour, External Organizations, ou_55236              
2Department of Cognitive Neuroscience, Radboud University Medical Centre, 6500 HB Nijmegen, The Netherlands, ou_persistent22              
3Neurogenetics of Vocal Communication Group, MPI for Psycholinguistics, Max Planck Society, ou_2231636              
4Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549              
5International Max Planck Research School for Language Sciences, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL, ou_1119545              
6Laboratory of Molecular Biology, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, 20892, USA, ou_persistent22              

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 Abstract: A steady accumulation of experimental data argues that protein synthesis in neurons is not merely restricted to the somatic compartment, but also occurs in several discrete cellular micro-domains. Local protein synthesis is critical for the establishment of synaptic plasticity in mature dendrites and in directing the growth cones of immature axons, and has been associated with cognitive impairment in mice and humans. Although in recent years a number of important mechanisms governing this process have been described, it remains technically challenging to precisely monitor local protein synthesis in individual neuronal cell parts independent from the soma. This report presents the utility of employing microfluidic chambers for the isolation and treatment of single neuronal cellular compartments. Furthermore, it is demonstrated that a protein synthesis assay, based on fluorescent non-canonical amino acid tagging (FUNCAT), can be combined with this cell culture system to label nascent proteins within a discrete structural and functional domain of the neuron. Together, these techniques could be employed for the detection of protein synthesis within developing and mature neurites, offering an effective approach to elucidate novel mechanisms controlling synaptic maintenance and plasticity.

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Language(s): eng - English
 Dates: 20162016
 Publication Status: Issued
 Pages: -
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 Rev. Type: Peer
 Identifiers: DOI: 10.1369/0022155416641604
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Title: Journal of Histochemistry and Cytochemistry
Source Genre: Journal
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Publ. Info: Seattle, WA : Histochemical Society
Pages: - Volume / Issue: 64 (5) Sequence Number: - Start / End Page: 323 - 333 Identifier: ISSN: 0022-1554
CoNE: https://pure.mpg.de/cone/journals/resource/954925414909