[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
Miller KG, Emerson MD, McManus JR, Rand JB (2000) Ric-8 (synembryn): a novel conserved protein that is required for G(q) alpha signaling in the C.elegans nervous system. Neuron 27: 289-299.
Miller KG, Rand JB (2000) A role for RIC-8 (synembryn) and GOA-1 (G(o)α) in regulating a subset of centrosome movements during early embryogenesis in Caenorhabditis elegans. Genetics 156: 1649-1660. (Pubitemid 32001232)
Miller KG, Alfonso A, Nguyen M, Crowell JA, Johson CD, Rand JB (1996) A genetic selection for Caenorhabditis elegans synaptic transmission mutants. Proc Natl Acad Sci USA 93: 12593-12598. (Pubitemid 26367189)
Tall GG, Krumins AM, Gilman AG (2003) Mammalian Ric-8A (Synembryn) is a heterotrimeric Gα protein guanine nucleotide exchange factor. J Biol Chem 278:8356-8362. (Pubitemid 36800584)
Klattenhoff C, Montecino M, Soto X, Guzmán L, Romo X, García MD, Mellstrom B, Naranjo JR, Hinrichs MV, Olate J (2003) Human synembryn interacts with Gsα and Gqα and is translocated to the plasma membrane in response to isoproterenol and carbachol. J Cell Physiol 195: 151-157. (Pubitemid 36384289)
Couwenbergs C, Spilker AC, Gotta M (2004) Control of embryonic spindle positioning and Gα activity by C.elegans RIC-8. Curr Biol 14: 1871-1876. (Pubitemid 39408778)
Tall GG, Gilman AG (2005) Resistance to inhibitors of cholinesterase 8A catalyzes release of Gαi-GTP and nuclear mitotic apparatus protein (NuMA) from NuMA/LGN/Gαi-GDP complexes. Proc Natl Acad Sci USA 102:16584-16589. (Pubitemid 41688820)
Afshar K, Willard FS, Colombo K, Johnston CA, McCudden CR, Siderovski DP, Gonczy P (2004) RIC-8 is required for GPR-1/2-dependent Galpha function during asymmetric division of C.elegans embryos. Cell 119:219-230. (Pubitemid 39360904)
David NB, Martin CA, Segalen M, Rosenfeld F, Schweisguth F, Bellaiche Y (2005) Drosophila Ric-8 regulates Galphai cortical localization to promote Galphai-dependent planar orientation of the mitotic spindle during asymmetric cell division. Nat Cell Biol 7: 1083-1090.
Hampoelz B, Hoeller O, Bowman SK, Dunican D, Knoblich JA (2005) Drosophila Ric-8 is essential for plasma-membrane localization of heterotrimeric G proteins. Nat Cell Biol 7: 1099-1105.
Wang H, Ng KH, Qian H, Siderovski DP, Chia W, Yu F (2005) Ric-8 controls Drosophila neural progenitor asymmetric division by regulating heterotrimeric G proteins. Nat Cell Biol 7: 1091-1098.
Blumer JB, Kuriyama R, Gettys TW, Lanier SM (2006) The G-protein regulatory (GPR) motif-containing Leu-Gly-Asn-enriched protein (LGN) and Giα3 influence cortical positioning of the mitotic spindle poles at metaphase in symmetrically dividing mammalian cells. Eur J Cell Biol 85: 1233-1240. (Pubitemid 44743146)
Malik S, Ghosh M, Bonacci TM, Tall GG, Smrcka AV (2005) Ric-8 enhances G protein βγ-dependent signaling in response to βγ-binding peptides in intact cells. Mol Pharmacol 68: 129-136. (Pubitemid 41002951)
Von Dannecker LE, Mercadante AF, Malnic B (2005) Ric-8B, an olfactory putative GTP exchange factor, amplifies signal transduction through the olfactory-specific G-protein Gαolf. J Neurosci 25: 3793-3800. (Pubitemid 40570412)
Nishimura A, Okamoto M, Sugawara Y, Mizuno N, Yamauchi J, Itoh H (2006) Ric-8A potentiates Gq-mediated signal transduction by acting downstream of G protein-coupled receptor in intact cells. Genes Cells 11:487-498.
Romo X, Pastén P, Martinez S, Soto X, Lara P, Ramirez A, Torrejón M, Montecino M, Hinrichs M, Olate J (2008) xRic-8 is a GEF for Gsα and participates in maintaining meiotic arrest in Xenopus laevis oocytes. J Cell Physiol 214: 673-680.
Andreeva A, Howorth D, Chandonia JM, Brenner SE, Hubbard TJ, Chothia C, Murzin AG (2008) Data growth and its impact on the SCOP database: new developments. Nucl Acids Res 36: D419-D425.
Peifer M, Ber S, Reynolds AB (1994) A repeating amino acid motif shared by proteins with diverse cellular roles. Cell 76: 789-791. (Pubitemid 24085316)
Ginalski K, Elofsson A, Fischer D, Rychlewski L (2003) 3D-Jury: a simple approach to improve protein structure predictions. Bioinformatics 19: 1015-1018. (Pubitemid 36675823)
Canutescu AA, Shelenkov AA, Dunbrack RL (2003) A graph theory algorithm for protein side-chain prediction. Protein Sci 12: 2001-2014. http://dunbrack.fccc.edu/SCWRL3.php. (Pubitemid 37022822)
Hess B, Kutzner C, van der Spoel D, Lindahl E (2008) GROMACS 4: algorithms for highly efficient, load-balanced, and scalable molecular simulation. J ChemTheory Comput 4: 435-447. http://www.gromacs.org.
Zhang Y (2008) I-TASSER server for protein 3D structure prediction. BMC Bioinformatics 23: 9-40. http://zhang.bioinformatics.ku.edu/I-TASSER.
Wiederstein M, Sippl MJ (2007) ProSA-web: interactive web service for the recognition of errors in three-dimensional structures of proteins. 35(Web Server issue): W407-W410.
Parmeggiani F, Pellarin R, Larsen AP, Varadamsetty G, Stumpp MT, Zerbe O, Caflisch A, Plückthun A (2008) Designed armadillo repeat proteins as general peptide-binding scaffolds: consensus design and computational optimization of the hydrophobic core J Mol Biol 376:1282-1304.
Vikis HG, Stewart S, Guan KL (2002) SmgGDS displays differential binding and exchange activity towards different Ras isoforms. Oncogene 21: 2425-2432. (Pubitemid 34407302)
Unneberg P, Merelo JJ, Chacón P, Morán F (2001) SOMCD: method for evaluating protein secondary structure from UV circular dichroism spectra. Proteins Struct Funct Genet 42: 460-470. (Pubitemid 32179856)
Kirchoff W (1993) EXAM: a two-state thermodynamic analysis program. Maryland: Gaithersburg.
Söding J, Biegert A, Lupas AN (2005) The HHpred interactive server for protein homology detection and structure prediction. Nucl Acids Res 33: W244-W248. http://toolkit.tuebingen.mpg.de/hhpred. (Pubitemid 44529917)
Ginalski K, Elofsson A, Fischer D, Rychlewski L (2003) 3D-Jury: a simple approach to improve protein structure predictions. Bioinformatics 19: 1015-1018. http://meta.bioinfo.pl/submit-wizard.pl. (Pubitemid 36675823)
McGuffin LJ, Bryson K, Jones DT (2000) The PSIPRED protein structure prediction server. Bioinformatics 16:404-405. http://bioinf.cs.ucl.ac.uk/ psipred/psiform.html. (Pubitemid 30417087)
Liu S, Zhang C, Liang S, Zhou Y (2007) Fold recognition by concurrent use of solvent accessibility and residue depth. Proteins 68: 636-645. http://sparks.informatics.iupui.edu/SP4. (Pubitemid 47068304)
Laskowski RA, MacArthur MW, Moss DS, Thornton JM (1993) PROCHECK: a program to check the stereo chemical quality of protein structures. J Appl Cryst 26:283-291.