Article (Scientific journals)
Biophysical studies support a predicted superhelical structure with armadillo repeats for Ric-8.
Figueroa, Maximiliano; Hinrichs, Maria Victoria; Bunster, Marta et al.
2009In Protein Science: A Publication of the Protein Society, 18 (6), p. 1139-45
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Keywords :
Animals; Armadillo Domain Proteins/chemistry; Caenorhabditis elegans Proteins/chemistry; Genetic Vectors; Models, Molecular; Nuclear Proteins/chemistry; Protein Structure, Secondary; Recombinant Proteins/chemistry
Abstract :
[en] Ric-8 is a highly conserved cytosolic protein (MW 63 KDa) initially identified in C. elegans as an essential factor in neurotransmitter release and asymmetric cell division. Two different isoforms have been described in mammals, Ric-8A and Ric-8B; each possess guanine nucleotide exchange activity (GEF) on heterotrimeric G-proteins, but with different Galpha subunits specificities. To gain insight on the mechanisms involved in Ric-8 cellular functions it is essential to obtain some information about its structure. Therefore, the aim of this work was to create a structural model for Ric-8. In this case, it was not possible to construct a model based on comparison with a template structure because Ric-8 does not present sequence similarity with any other protein. Consequently, different bioinformatics approaches that include protein folding and structure prediction were used. The Ric-8 structural model is composed of 10 armadillo folding motifs, organized in a right-twisted alpha-alpha super helix. In order to validate the structural model, a His-tag fusion construct of Ric-8 was expressed in E. coli, purified by affinity and anion exchange chromatography and subjected to circular dichroism analysis (CD) and thermostability studies. Ric-8 is approximately 80% alpha helix, with a Tm of 43.1 degrees C, consistent with an armadillo-type structure such as alpha-importin, a protein composed of 10 armadillo repeats. The proposed structural model for Ric-8 is intriguing because armadillo proteins are known to interact with multiple partners and participate in diverse cellular functions. These results open the possibility of finding new protein partners for Ric-8 with new cellular functions.
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Figueroa, Maximiliano ;  Université de Liège - ULiège > Département des sciences de la vie > GIGA-R : Biologie et génétique moléculaire
Hinrichs, Maria Victoria
Bunster, Marta
Babbitt, Patricia
Martinez-Oyanedel, Jose
Olate, Juan
Language :
English
Title :
Biophysical studies support a predicted superhelical structure with armadillo repeats for Ric-8.
Publication date :
2009
Journal title :
Protein Science: A Publication of the Protein Society
ISSN :
0961-8368
eISSN :
1469-896X
Publisher :
Cold Spring Harbor Laboratory Press, Woodbury, United States - New York
Volume :
18
Issue :
6
Pages :
1139-45
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 07 February 2012

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