Literature DB >> 21985762

Measuring CaMKII concentration in dendritic spines.

Nikolai Otmakhov1, John Lisman.   

Abstract

Here, we present a method for measuring the concentration of endogenous protein in cellular compartments. Importantly, the method is applicable to compartments such as dendritic spines with dimensions often close to the resolution limit of optical microscopy. To our knowledge, a method with such capabilities has not yet been described. The method utilizes overexpression of the protein of interest, which is tagged with fluorescent protein. This is followed by immunostaining of both overexpressed and endogenous proteins. Expression of a volume marker is also required. We applied this method to measure the concentration of Ca/calmodulin kinase II (CaMKII) in different cellular compartments of hippocampal pyramidal neurons. It was found that the concentrations of CaMKIIα subunits in cell bodies, proximal dendrites, and spines on these dendrites are 71, 46, and 103 μM, respectively. Considering the 3:1 ratio of α to β CaMKII subunits in the hippocampus, the concentrations of total (α+β) CaMKII subunits in these compartments are 94, 61, and 138 μM, respectively.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21985762      PMCID: PMC3221876          DOI: 10.1016/j.jneumeth.2011.09.022

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  15 in total

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3.  Determination of absolute protein numbers in single synapses by a GFP-based calibration technique.

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4.  Autonomous CaMKII can promote either long-term potentiation or long-term depression, depending on the state of T305/T306 phosphorylation.

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5.  Dendritic spines of CA 1 pyramidal cells in the rat hippocampus: serial electron microscopy with reference to their biophysical characteristics.

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8.  Persistent accumulation of calcium/calmodulin-dependent protein kinase II in dendritic spines after induction of NMDA receptor-dependent chemical long-term potentiation.

Authors:  Nikolai Otmakhov; Jung-Hwa Tao-Cheng; Stephen Carpenter; Brent Asrican; Ayse Dosemeci; Thomas S Reese; John Lisman
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  13 in total

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6.  Excitotoxic insult results in a long-lasting activation of CaMKIIα and mitochondrial damage in living hippocampal neurons.

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7.  Development of a molecularly evolved, highly sensitive CaMKII FRET sensor with improved expression pattern.

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Review 8.  Criteria for identifying the molecular basis of the engram (CaMKII, PKMzeta).

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9.  Activation-triggered subunit exchange between CaMKII holoenzymes facilitates the spread of kinase activity.

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10.  Multiple CaMKII Binding Modes to the Actin Cytoskeleton Revealed by Single-Molecule Imaging.

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