Showing papers by "Francis S. Willard published in 2006"

Minimal determinants for binding activated G alpha from the structure of a G alpha(i1)-peptide dimer.

Abstract: G-proteins cycle between an inactive GDP-bound state and an active GTP-bound state, serving as molecular switches that coordinate cellular signaling. We recently used phage display to identify a series of peptides that bind G alpha subunits in a nucleotide-dependent manner [Johnston, C. A., Willard, F. S., Jezyk, M. R., Fredericks, Z., Bodor, E. T., Jones, M. B., Blaesius, R., Watts, V. J., Harden, T. K., Sondek, J., Ramer, J. K., and Siderovski, D. P. (2005) Structure 13, 1069-1080]. Here we describe the structural features and functions of KB-1753, a peptide that binds selectively to GDP x AlF4(-)- and GTPgammaS-bound states of G alpha(i) subunits. KB-1753 blocks interaction of G alpha(transducin) with its effector, cGMP phosphodiesterase, and inhibits transducin-mediated activation of cGMP degradation. Additionally, KB-1753 interferes with RGS protein binding and resultant GAP activity. A fluorescent KB-1753 variant was found to act as a sensor for activated G alpha in vitro. The crystal structure of KB-1753 bound to G alpha(i1) x GDP x AlF4(-) reveals binding to a conserved hydrophobic groove between switch II and alpha3 helices and, along with supporting biochemical data and previous structural analyses, supports the notion that this is the site of effector interactions for G alpha(i) subunits.

Does WAVE1 contain a GoLoco/GPR motif?

Abstract: Heterotrimeric G-protein alpha subunits (Gα) are molecular switches regulated by the binding and hydrolysis of guanosine 5-triphosphate 1. Non-receptor proteins that modulate the nucleotide binding and hydrolysis activities of Gα proteins have recently become of considerable interest 2, 3. One class of Gα modulating proteins is defined by the presence of a GoLoco motif(s) in their primary sequence 4. The GoLoco motif was discovered as a region of sequence homology within novel Gα-binding proteins 5-7, and is also referred to as the G-protein regulatory (GPR) motif 5. The GoLoco motif is a peptide of 20-40 amino acids that binds Gαi/o•GDP and prevents the spontaneous release of GDP by Gα, thus acting as a guanine nucleotide dissociation inhibitor (GDI) (reviewed in 4). To date, GoLoco/GPR motifs are known to exist in four well-defined families of proteins (Fig. ​(Fig.1).1). (1) Single GoLoco motifs are present in the RGS and RBD domain containing proteins RGS12, RGS14, and Drosophila Loco (Fig. ​(Fig.1).1). (2) PCP-2/GPSM4 and GPSM3/G18 contain two or three GoLoco motifs respectively, but no other currently identifiable functional domains or sequence motifs (Fig. ​(Fig.1).1). (3) Single GoLoco motifs are present in the N-termini of RapGAP domain-containing proteins (Rap1GAP1a, -b and Rap1GAP2b, -c) (Fig. ​(Fig.1).1). (4) The GoLoco motif is found in multiple arrays in the tetratricopeptide-repeat (TPR) domain containing proteins PINS (Partner of Inscuteable), GPSM2/LGN, and GPSM1/AGS3 (Fig. ​(Fig.11). Figure 1 The predicted domain architecture of all human GoLoco motif containing proteins. Domain boundaries were determined using BLAST 17, SMART 9, and ClustalW 18. Song et al., recently described the presence of a GoLoco/GPR motif in the actin polymerization regulating protein WAVE1 8. A synthetic peptide corresponding to this putative WAVE1 GoLoco motif was found to have GDI activity for Gαi1,2,3 in vitro. Furthermore, in coimmunoprecipitation experiments full length WAVE1 was found to interact with Gαi3•GDP but not Gαi3•GTPγS in both COS-7 cell lysates and rat brain extracts 8. Primary sequence analysis of WAVE1 (a.k.a. SCAR1) indicates that, in many ways, does conform to the GoLoco motif consensus sequence (Fig. ​(Fig.2A).2A). WAVE1 contains a predicted alpha helical region that is terminated by a glutamine residue. Subsequently a [R]-[K]-[aliphatic]-[DE]-[DE]-[Q]-[R] motif characteristic of many GoLoco motifs is present. However, upon further analysis of the primary sequence of WAVE1 it can be observed that the predicted GoLoco/GPR motif overlaps the WASP homology 2 (WH2) domain (Fig. ​(Fig.2B)2B) 8. The C-terminal domain architecture consisting of a WH2-domain, central domain, and acidic domain (also referred to as the VCA region) is characteristic of proteins such as WAVE1-3, WASP, and N-WASP that stimulate Arp2/3-dependent actin nucleation 10. The WH2 and central regions interact with actin monomers 11, 12 whereas Arp2/3 binds to the central and acidic domains of WAVE/WASP proteins 13 (binding sites are illustrated in Fig ​Fig2C).2C). The structure and function of the WH2-central-acidic cassette in actin nucleating proteins is highly conserved throughout evolution 14. Figure 2 (A) Structure-based multiple sequence alignment of quintessential GoLoco motifs and the putative GoLoco motif of human WAVE1. Alpha symbols (α) and asterisks (*) denote alpha helical secondary structure and GoLoco motif contacts with Gα ... As the WH2 domain of WAVE1 directly overlies the predicted GoLoco/GPR motif described by Song et al. 8 (Fig ​(Fig2B,2B, C), logic states that WAVE1 can either contain a WH2 domain or a GoLoco motif but not both. Available biochemical and structural evidence strongly suggests that WAVE1 contains a functional WH2 domain that binds actin monomers with low micromolar affinity, or with nanomolar affinity in the context of an extended WH2 domain containing the central region 12. Given that WAVE1, 2 and 3 contain the only WH2 domains similar in sequence to GoLoco/GPR motifs, it must be considered highly unlikely that WAVE1 contains a bona fide GoLoco/GPR motif. A simple explanation is that WAVE1 contains a WH2 domain with fortuitous sequence similarity to GoLoco/GPR motifs. That is not to say that the WAVE1/Gαi interactions observed by Song et al. 8 should not be considered important. One could consider this intriguing dual usage of a WH2 domain as a possible case of convergent evolution. In terms of the known structural biology of WH2/actin and Gα/GoLoco complexes this is not out of the question. Both the WH2 domain and GoLoco motif are likely in a unstructured conformation when unbound to ligand 11, 15, 16; thus it is possible that Gαi and actin could compete for WH2 domain binding. It is worth noting, however, that despite high levels of sequence identity between the three human WAVE isoform WH2 domains (Fig. ​(Fig.1C)1C) only WAVE1 but not WAVE2 nor WAVE3 were found to have GDI activity on Gαi subunits (the signature biochemical activity of a GoLoco/GPR motif). This therefore argues against a conserved role for WH2 domains in heterotrimeric G-protein regulation, in general. In summary, WH2 domains and GoLoco/GPR motifs are evolutionarily independent protein-binding sequences. Fortuitous sequence similarity between WH2 domains and GoLoco/GPR motifs should not be considered indicative of common ancestry and/or shared function.