A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS

<p>Abstract</p> <p>Background</p> <p>Proteomic analysis of laticifer latex in <it>Hevea brasiliensis </it>has been received more significant attentions. However, the sticky and viscous characteristic of rubber latex as cytoplasm of laticifer cells and the co...

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Main Authors: Guo Anping, Wu Chenggong, Ma Ruifeng, Lu Xiuli, Shi Minjing, Wang Xuchu, Peng Ming, Tian Weimin
Format: Article
Language:English
Published: BMC 2010-06-01
Series:Proteome Science
Online Access:http://www.proteomesci.com/content/8/1/35
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spelling doaj-c88652bc8fde4cfb81f61e000fba55f72020-11-24T21:35:58ZengBMCProteome Science1477-59562010-06-01813510.1186/1477-5956-8-35A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MSGuo AnpingWu ChenggongMa RuifengLu XiuliShi MinjingWang XuchuPeng MingTian Weimin<p>Abstract</p> <p>Background</p> <p>Proteomic analysis of laticifer latex in <it>Hevea brasiliensis </it>has been received more significant attentions. However, the sticky and viscous characteristic of rubber latex as cytoplasm of laticifer cells and the complication of laticifer latex membrane systems has made it challenge to isolate high-quality proteins for 2-DE and MS.</p> <p>Results</p> <p>Based on the reported Borax/PVPP/Phenol (BPP) protocol, we developed an efficient method for protein preparation from different latex subcellular fractions and constructed high-resolution reference 2-DE maps. The obtained proteins from both total latex and C-serum fraction with this protocol generate more than one thousand protein spots and several hundreds of protein spots from rubber particles as well as lutoid fraction and its membranes on the CBB stained 2-DE gels. The identification of 13 representative proteins on 2-DE gels by MALDI TOF/TOF MS/MS suggested that this method is compatible with MS.</p> <p>Conclusion</p> <p>The proteins extracted by this method are compatible with 2-DE and MS. This protein preparation protocol is expected to be used in future comparative proteomic analysis for natural rubber latex.</p> http://www.proteomesci.com/content/8/1/35
collection DOAJ
language English
format Article
sources DOAJ
author Guo Anping
Wu Chenggong
Ma Ruifeng
Lu Xiuli
Shi Minjing
Wang Xuchu
Peng Ming
Tian Weimin
spellingShingle Guo Anping
Wu Chenggong
Ma Ruifeng
Lu Xiuli
Shi Minjing
Wang Xuchu
Peng Ming
Tian Weimin
A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS
Proteome Science
author_facet Guo Anping
Wu Chenggong
Ma Ruifeng
Lu Xiuli
Shi Minjing
Wang Xuchu
Peng Ming
Tian Weimin
author_sort Guo Anping
title A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS
title_short A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS
title_full A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS
title_fullStr A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS
title_full_unstemmed A method for protein extraction from different subcellular fractions of laticifer latex in <it>Hevea brasiliensis </it>compatible with 2-DE and MS
title_sort method for protein extraction from different subcellular fractions of laticifer latex in <it>hevea brasiliensis </it>compatible with 2-de and ms
publisher BMC
series Proteome Science
issn 1477-5956
publishDate 2010-06-01
description <p>Abstract</p> <p>Background</p> <p>Proteomic analysis of laticifer latex in <it>Hevea brasiliensis </it>has been received more significant attentions. However, the sticky and viscous characteristic of rubber latex as cytoplasm of laticifer cells and the complication of laticifer latex membrane systems has made it challenge to isolate high-quality proteins for 2-DE and MS.</p> <p>Results</p> <p>Based on the reported Borax/PVPP/Phenol (BPP) protocol, we developed an efficient method for protein preparation from different latex subcellular fractions and constructed high-resolution reference 2-DE maps. The obtained proteins from both total latex and C-serum fraction with this protocol generate more than one thousand protein spots and several hundreds of protein spots from rubber particles as well as lutoid fraction and its membranes on the CBB stained 2-DE gels. The identification of 13 representative proteins on 2-DE gels by MALDI TOF/TOF MS/MS suggested that this method is compatible with MS.</p> <p>Conclusion</p> <p>The proteins extracted by this method are compatible with 2-DE and MS. This protein preparation protocol is expected to be used in future comparative proteomic analysis for natural rubber latex.</p>
url http://www.proteomesci.com/content/8/1/35
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