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Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions

BACKGROUND: Dorsal root ganglion (DRG) neurons are primary sensory neurons that conduct neuronal impulses related to pain, touch and temperature senses. Plasma membrane (PM) of DRG cells plays important roles in their functions. PM proteins are main performers of the functions. However, mainly due t...

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Autores principales: Xiong, Xia, Huang, Sha, Zhang, Hai, Li, Jianjun, Shen, Jianying, Xiong, Jixian, Lin, Yong, Jiang, Liping, Wang, Xianchun, Liang, Sonping
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780401/
https://www.ncbi.nlm.nih.gov/pubmed/19889238
http://dx.doi.org/10.1186/1477-5956-7-41
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author Xiong, Xia
Huang, Sha
Zhang, Hai
Li, Jianjun
Shen, Jianying
Xiong, Jixian
Lin, Yong
Jiang, Liping
Wang, Xianchun
Liang, Sonping
author_facet Xiong, Xia
Huang, Sha
Zhang, Hai
Li, Jianjun
Shen, Jianying
Xiong, Jixian
Lin, Yong
Jiang, Liping
Wang, Xianchun
Liang, Sonping
author_sort Xiong, Xia
collection PubMed
description BACKGROUND: Dorsal root ganglion (DRG) neurons are primary sensory neurons that conduct neuronal impulses related to pain, touch and temperature senses. Plasma membrane (PM) of DRG cells plays important roles in their functions. PM proteins are main performers of the functions. However, mainly due to the very low amount of DRG that leads to the difficulties in PM sample collection, few proteomic analyses on the PM have been reported and it is a subject that demands further investigation. RESULTS: By using aqueous polymer two-phase partition in combination with high salt and high pH washing, PMs were efficiently enriched, demonstrated by western blot analysis. A total of 954 non-redundant proteins were identified from the plasma membrane-enriched preparation with CapLC-MS/MS analysis subsequent to protein separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) or shotgun digestion. 205 (21.5%) of the identified proteins were unambiguously assigned as PM proteins, including a large number of signal proteins, receptors, ion channel and transporters. CONCLUSION: The aqueous polymer two-phase partition is a simple, rapid and relatively inexpensive method. It is well suitable for the purification of PMs from small amount of tissues. Therefore, it is reasonable for the DRG PM to be enriched by using aqueous two-phase partition as a preferred method. Proteomic analysis showed that DRG PM was rich in proteins involved in the fundamental biological processes including material exchange, energy transformation and information transmission, etc. These data would help to our further understanding of the fundamental DRG functions.
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spelling pubmed-27804012009-11-21 Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions Xiong, Xia Huang, Sha Zhang, Hai Li, Jianjun Shen, Jianying Xiong, Jixian Lin, Yong Jiang, Liping Wang, Xianchun Liang, Sonping Proteome Sci Research BACKGROUND: Dorsal root ganglion (DRG) neurons are primary sensory neurons that conduct neuronal impulses related to pain, touch and temperature senses. Plasma membrane (PM) of DRG cells plays important roles in their functions. PM proteins are main performers of the functions. However, mainly due to the very low amount of DRG that leads to the difficulties in PM sample collection, few proteomic analyses on the PM have been reported and it is a subject that demands further investigation. RESULTS: By using aqueous polymer two-phase partition in combination with high salt and high pH washing, PMs were efficiently enriched, demonstrated by western blot analysis. A total of 954 non-redundant proteins were identified from the plasma membrane-enriched preparation with CapLC-MS/MS analysis subsequent to protein separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) or shotgun digestion. 205 (21.5%) of the identified proteins were unambiguously assigned as PM proteins, including a large number of signal proteins, receptors, ion channel and transporters. CONCLUSION: The aqueous polymer two-phase partition is a simple, rapid and relatively inexpensive method. It is well suitable for the purification of PMs from small amount of tissues. Therefore, it is reasonable for the DRG PM to be enriched by using aqueous two-phase partition as a preferred method. Proteomic analysis showed that DRG PM was rich in proteins involved in the fundamental biological processes including material exchange, energy transformation and information transmission, etc. These data would help to our further understanding of the fundamental DRG functions. BioMed Central 2009-11-05 /pmc/articles/PMC2780401/ /pubmed/19889238 http://dx.doi.org/10.1186/1477-5956-7-41 Text en Copyright ©2009 Xiong et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xiong, Xia
Huang, Sha
Zhang, Hai
Li, Jianjun
Shen, Jianying
Xiong, Jixian
Lin, Yong
Jiang, Liping
Wang, Xianchun
Liang, Sonping
Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
title Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
title_full Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
title_fullStr Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
title_full_unstemmed Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
title_short Enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
title_sort enrichment and proteomic analysis of plasma membrane from rat dorsal root ganglions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780401/
https://www.ncbi.nlm.nih.gov/pubmed/19889238
http://dx.doi.org/10.1186/1477-5956-7-41
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