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...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2010-06-01
|
Series: | Proteome Science |
Online Access: | http://www.proteomesci.com/content/8/1/35 |
id |
doaj-c88652bc8fde4cfb81f61e000fba55f7 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT guoanping amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT wuchenggong amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT maruifeng amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT luxiuli amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT shiminjing amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT wangxuchu amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT pengming amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT tianweimin amethodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT guoanping methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT wuchenggong methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT maruifeng methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT luxiuli methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT shiminjing methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT wangxuchu methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT pengming methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms AT tianweimin methodforproteinextractionfromdifferentsubcellularfractionsoflaticiferlatexinitheveabrasiliensisitcompatiblewith2deandms |
_version_ |
1725943115536138240 |