Quantitative proteomic profiling of membrane proteins from the mouse brain cortex, hippocampus, and cerebellum using the HysTag reagent: mapping of neurotransmitter receptors and ion channels

Jesper Velgaard Olsen; Peter Aa Nielsen; Jens Roswalld Andersen; Matthias Mann; Jacek R Wisniewski

doi:10.1016/j.brainres.2006.11.082

Quantitative proteomic profiling of membrane proteins from the mouse brain cortex, hippocampus, and cerebellum using the HysTag reagent: mapping of neurotransmitter receptors and ion channels

Jesper Velgaard Olsen, Peter Aa Nielsen, Jens Roswalld Andersen, Matthias Mann, Jacek R Wisniewski

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

38 Citationer (Scopus)

Abstract

Udgivelsesdato: 2007-Feb-23

Originalsprog	Engelsk
Tidsskrift	Brain Research
Vol/bind	1134
Udgave nummer	1
Sider (fra-til)	95-106
Antal sider	11
ISSN	0006-8993
DOI	https://doi.org/10.1016/j.brainres.2006.11.082
Status	Udgivet - 2007
Udgivet eksternt	Ja

Bibliografisk note

Keywords: Animals; Cerebellum; Cerebral Cortex; Female; Hippocampus; Indicators and Reagents; Ion Channels; Membrane Proteins; Mice; Mice, Inbred C57BL; Proteomics; Receptors, Neurotransmitter; Subcellular Fractions

Adgang til dokumentet

10.1016/j.brainres.2006.11.082

Citationsformater

Quantitative proteomic profiling of membrane proteins from the mouse brain cortex, hippocampus, and cerebellum using the HysTag reagent: mapping of neurotransmitter receptors and ion channels. / Olsen, Jesper Velgaard; Nielsen, Peter Aa; Andersen, Jens Roswalld; Mann, Matthias; Wisniewski, Jacek R.

I: Brain Research, Bind 1134, Nr. 1, 2007, s. 95-106.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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title = "Quantitative proteomic profiling of membrane proteins from the mouse brain cortex, hippocampus, and cerebellum using the HysTag reagent: mapping of neurotransmitter receptors and ion channels",

abstract = "Analysis of the brain proteome and studying brain diseases through clinical biopsies and animal disease models require methods of quantitative proteomics that are sensitive and allow identification and quantification of low abundant membrane proteins from minute amount of tissue. Taking advantage of recently developed methods for isolation of membrane proteins from 10-20 mg brain tissue [Nielsen, P.Aa., Olsen, J.V., Podtelejnokov, A.V., Andersen, J.R., Mann, M., Wisniewski, J.R., 2005. Proteomic mapping of brain plasma membrane proteins. Mol. Cell. Proteomics 4, 402--408] and the HysTag-quantification method [Olsen, J.V., Andersen, J.R., Nielsen, P.Aa., Nielsen, M.L., Figeys, D., Mann, M., Wisniewski, J.R., 2004. HysTag---A novel proteomic qualification tool applied to differential analysis of membrane proteins from distinct areas of mouse brain. Mol. Cell. Proteomics 3, 82--92] we performed quantitative proteomic analysis of three functionally distinct compartments of mouse brain: cortex, hippocampus, and cerebellum. In total, 976 unique peptides corresponding to 555 unique proteins were quantified. Up to 20-fold differences in the levels of some proteins between brain areas were measured. For many quantified proteins--as for glutamate receptors, calcium channel subunits, and ATP-ases--an excellent correlation between our proteomic data and previously published mRNA expression levels or intensity of immunostaining was found. Our results clearly demonstrate differences in levels of membrane proteins mapped in distinct brain compartments and offer a technology that allows in depth study of brain membrane proteomes, such as mouse models of neurological diseases.",

author = "Olsen, {Jesper Velgaard} and Nielsen, {Peter Aa} and Andersen, {Jens Roswalld} and Matthias Mann and Wisniewski, {Jacek R}",

note = "Keywords: Animals; Cerebellum; Cerebral Cortex; Female; Hippocampus; Indicators and Reagents; Ion Channels; Membrane Proteins; Mice; Mice, Inbred C57BL; Proteomics; Receptors, Neurotransmitter; Subcellular Fractions",

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T1 - Quantitative proteomic profiling of membrane proteins from the mouse brain cortex, hippocampus, and cerebellum using the HysTag reagent: mapping of neurotransmitter receptors and ion channels

AU - Olsen, Jesper Velgaard

AU - Nielsen, Peter Aa

AU - Andersen, Jens Roswalld

AU - Mann, Matthias

AU - Wisniewski, Jacek R

N1 - Keywords: Animals; Cerebellum; Cerebral Cortex; Female; Hippocampus; Indicators and Reagents; Ion Channels; Membrane Proteins; Mice; Mice, Inbred C57BL; Proteomics; Receptors, Neurotransmitter; Subcellular Fractions

PY - 2007

Y1 - 2007

N2 - Analysis of the brain proteome and studying brain diseases through clinical biopsies and animal disease models require methods of quantitative proteomics that are sensitive and allow identification and quantification of low abundant membrane proteins from minute amount of tissue. Taking advantage of recently developed methods for isolation of membrane proteins from 10-20 mg brain tissue [Nielsen, P.Aa., Olsen, J.V., Podtelejnokov, A.V., Andersen, J.R., Mann, M., Wisniewski, J.R., 2005. Proteomic mapping of brain plasma membrane proteins. Mol. Cell. Proteomics 4, 402--408] and the HysTag-quantification method [Olsen, J.V., Andersen, J.R., Nielsen, P.Aa., Nielsen, M.L., Figeys, D., Mann, M., Wisniewski, J.R., 2004. HysTag---A novel proteomic qualification tool applied to differential analysis of membrane proteins from distinct areas of mouse brain. Mol. Cell. Proteomics 3, 82--92] we performed quantitative proteomic analysis of three functionally distinct compartments of mouse brain: cortex, hippocampus, and cerebellum. In total, 976 unique peptides corresponding to 555 unique proteins were quantified. Up to 20-fold differences in the levels of some proteins between brain areas were measured. For many quantified proteins--as for glutamate receptors, calcium channel subunits, and ATP-ases--an excellent correlation between our proteomic data and previously published mRNA expression levels or intensity of immunostaining was found. Our results clearly demonstrate differences in levels of membrane proteins mapped in distinct brain compartments and offer a technology that allows in depth study of brain membrane proteomes, such as mouse models of neurological diseases.

AB - Analysis of the brain proteome and studying brain diseases through clinical biopsies and animal disease models require methods of quantitative proteomics that are sensitive and allow identification and quantification of low abundant membrane proteins from minute amount of tissue. Taking advantage of recently developed methods for isolation of membrane proteins from 10-20 mg brain tissue [Nielsen, P.Aa., Olsen, J.V., Podtelejnokov, A.V., Andersen, J.R., Mann, M., Wisniewski, J.R., 2005. Proteomic mapping of brain plasma membrane proteins. Mol. Cell. Proteomics 4, 402--408] and the HysTag-quantification method [Olsen, J.V., Andersen, J.R., Nielsen, P.Aa., Nielsen, M.L., Figeys, D., Mann, M., Wisniewski, J.R., 2004. HysTag---A novel proteomic qualification tool applied to differential analysis of membrane proteins from distinct areas of mouse brain. Mol. Cell. Proteomics 3, 82--92] we performed quantitative proteomic analysis of three functionally distinct compartments of mouse brain: cortex, hippocampus, and cerebellum. In total, 976 unique peptides corresponding to 555 unique proteins were quantified. Up to 20-fold differences in the levels of some proteins between brain areas were measured. For many quantified proteins--as for glutamate receptors, calcium channel subunits, and ATP-ases--an excellent correlation between our proteomic data and previously published mRNA expression levels or intensity of immunostaining was found. Our results clearly demonstrate differences in levels of membrane proteins mapped in distinct brain compartments and offer a technology that allows in depth study of brain membrane proteomes, such as mouse models of neurological diseases.

U2 - 10.1016/j.brainres.2006.11.082

DO - 10.1016/j.brainres.2006.11.082

M3 - Journal article

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VL - 1134

SP - 95

EP - 106

JO - Brain Research

JF - Brain Research

SN - 0006-8993

IS - 1

ER -