Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/11476

TitleExpression of the functional carbohydrate-binding module (CBM) of human laforin
Author(s)Moreira, Susana Margarida Gomes
Castanheira, Pedro
Casal, Margarida
Faro, Carlos
Gama, F. M.
KeywordsLaforin
Carbohydrate-binding module
RGD
Inclusion bodies
Issue date2010
PublisherElsevier
JournalProtein Expression and Purification
Citation"Protein Expression and Purification". ISSN 1046-5928. 74:2 (2010) 169-174.
Abstract(s)Laforin is a human protein associated with the glycogen metabolism, composed of two structurally and functionally independent domains: a phosphatase catalytic domain and a substrate-binding module with glycogen and starch affinity. The main goal of this work is the development of a methodology for the expression of the so far poorly characterized carbohydrate-binding module (CBM) of laforin, allowing its study and development of biomedical applications. The laforin’s CBM sequence was originally cloned by PCR from a human muscle cDNA library. The recombinant protein, containing laforin’s CBM fused to an Arg-Gly-Asp sequence (RGD), was cloned and expressed using vector pET29a and recovered as inclusion bodies (IBs). Refolding of the IBs allowed the purification of soluble, dimeric and functional protein, according to adsorption assays using starch and glycogen. Several other experimental approaches, using both bacteria and yeast, were unsuccessfully tested, pointing towards the difficulties in producing the heterologous protein. Indeed, this is the first work reporting the production of the functional CBM from human laforin.
TypeArticle
URIhttp://hdl.handle.net/1822/11476
DOI10.1016/j.pep.2010.06.019
ISSN1046-5928
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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