Non-muscle myosin II (NM-II) is present in every cell type and moves actin filaments to provide contraction within the cell. NM-II has a motor domain, a neck domain that binds two light chains, a long coiled-coil tail domain, and a carboxyl-terminal tailpiece. NM-II forms bipolar filaments by associating near the carboxyl-terminus of the tail. It has long been known that both the formation of bipolar filaments and enzymatic activity of the motor domain are regulated by phosphorylation of one of the neck-binding light chains, known as the regulatory light chain (RLC). This phosphorylation causes a large-scale conformational shift of both the motor domains and the tail domain. However, the mechanism of this regulation and the elements that mediate the autoinhibition remain unknown. We have taken a deletional approach to finding the elements necessary for autoinhibition and regulation of filament assembly. We have used salt- dependent pelleting assays, cell culture, and analytical ultracentrifugation to identify two small regions in the IQ motifs of the neck and the carboxyl-terminal tailpiece that are essential for autoinhibition. Another necessary element for autoinhibition is the fold the coiled coil of the tail back on itself by means of hinge domains. We used internal deletions, pelleting assays, and thermal stability assays to identify and characterize the flexible hinge domains within the coiled-coil tail of NM-II. These hinges consist of low-stability regions of coiled coil, and can be stiffened by introducing mutations that cause the sequence to mimic a more ideal coiled coil. By defining these essential elements of autoinhibition, this work paves the way for a mechanistic understanding of the complex regulation of NM-II in the cell. This dissertation contains unpublished co-authored material. / 2015-07-11

Étude moléculaire des étapes précoces de la symbiose actinorhizienne Casuarina-Frankia : analyse fonctionnelle des gènes de la plante hôte contrôlant l'infectionPlus de 80% des plantes peuvent établir une symbiose racinaire avec des champignons de l'ordre des Glomales et former des endomycorhizes à arbuscules (AM). En revanche, seules certaines espèces appartenant à dix familles d'angiospermes réunies dans le Clade des Eurosidées I peuvent établir une symbiose racinaire fixatrice d'azote. Il s'agit d'une part, des plantes de la famille des légumineuses (Fabacées) et de Parasponia associées à Rhizobium et d'autre part, des plantes actinorhiziennes associées à l'actinomycète Frankia. Comme chez les légumineuses, la symbiose actinorhizienne aboutit à la formation de nodosités (ou « nodules »), siège de la fixation d'azote par les bactéries. Cependant, contrairement aux nodules des légumineuses, le nodule actinorhizien présente une structure et un développement s'apparentant aux racines latérales. L'étude des nodosités actinorhiziennes est donc particulièrement intéressante tant pour rechercher les spécificités de cette symbiose, que pour déterminer quelles sont les caractéristiques communes avec les légumineuses. Nous avons étudié le rôle du gène CCaMK dans le processus symbiotique et l'organogenèse nodulaire chez l'arbre actinorhizien Casuarina glauca. CCaMK code pour une protéine kinase dépendante du calcium et de la calmoduline (« calcium and calmodulin dependent protein kinase »). Dans la cascade de signalisation conduisant à la nodulation et à la mycorhization chez les légumineuses, ce gène est positionné en aval des oscillations calciques (« calcium spiking ») qui ont lieu durant les premières étapes de l'interaction symbiotique. CCaMK jouerait un rôle dans la perception et le décodage des oscillations calciques, ainsi que leur transduction aux différents composants contrôlant les endosymbioses racinaires. Nous avons suivi l'expression spatio-temporelle de la fusion transcriptionnelle PromCgCCaMK::GUS au cours de la nodulation et montré que celle-ci était corrélée à la présence de Frankia tout au long du processus symbiotique, soulignant ainsi le rôle clé de CCaMK dans l'infection. Par ailleurs, nous avons cherché à déterminer l'importance du domaine autoinhibiteur de la protéine CCaMK dans l'activation du processus d'organogenèse du nodule. Pour cela, nous avons réalisé et introduit chez C. glauca des constructions géniques de CgCCaMK permettant l'expression de formes tronquées constitutivement actives, car dépourvues du domaine autoinhibiteur/CaM. Nous avons aussi utilisé des formes tronquées du gène MtCCaMK de Medicago truncatula. L'expression de ces formes tronquées de CCaMK a révélé que la levée de l'autoinhibition induit la formation de nodules spontanés indépendamment de l'actinobactérie Frankia. Les résultats obtenus suggèrent que la protéine dérégulée est capable de réactiver la voie de signalisation, ainsi que les gènes situés en aval de CCaMK, qui sont nécessaires à l'organogenèse nodulaire.Mots clés : Casuarina glauca, Frankia, CCaMK, infection, autoinhibition, nodules spontanés / Molecular study of the early stages of actinorhizal symbiosis Casuarina-Frankia: functional analysis of the host plant genes controlling the infectionMore than 80% of plant species are able to develop arbuscular mycorrhizal (AM) symbiosis in association with glomeromycete fungi. In contrast, only some species of the Eurosid I clade, confined to four orders and ten Angiosperm families, are able to form nitrogen-fixing root nodule symbioses with soil bacteria. This concerns plants of the legume family (Fabaceae) and Parasponia associated with Rhizobium bacteria and actinorhizal plants associated with the actinomycete Frankia. Similarly to Legumes, the actinorhizal symbiosis results in the formation of nitrogen-fixing root nodules. However, unlike legume nodule, the actinorhizal nodule has a same origin and structure than a lateral root. Thus, the study of actinorhizal nodules is of particular interest not only for investigating its specific properties but also, for determining common characteristics shared with legume nodules.We have studied the role of CgCCaMK gene during the symbiotic process and nodule organogenesis in the actinorhizal tree Casuarina glauca. CCaMK encodes a calcium and calmodulin dependent protein kinase. In the signalisation cascade leading to both nodulation and mycorrhization in legumes, this gene is acting downstream the calcium oscillations (« calcium spiking ») that occur during the early steps of the symbiotic interaction. It has been suggested that these calcium oscillations are decoded and transduced by the CCaMK protein.We have monitored the spatio-temporal expression of a PromCgCCaMK::GUS fusion during actinorhizal nodulation and have shown that reporter gene expression was correlated with the presence of Frankia along the symbiotic process. This data highlights the role of CgCCaMK during Frankia infection. In addition, we have investigated the role of the CCaMK autoinhibitory/CaM domain in actinorhizal nodule organogenesis. To achieve this goal, we have obtained truncated versions of CgCCaMK lacking the autoinhibitory/CaM domain, and then expressed them into C. glauca. We have also used truncated forms of MtCCaMK from Medicago truncatula. The expression of these CCaMK constructs from C. glauca and M. truncatula was found to induce spontaneous nodulation in the absence of Frankia bacteria. These results suggest that deregulation of the calcium and calmodulin dependent protein kinase is able to reactivate the symbiotic signalling pathway and genes acting downstream CCaMK that are needed for nodule organogenesis.Key words: Casuarina glauca, Frankia, CCaMK, infection, autoinhibition, spontaneous nodules

Inorganic cations play decisive roles in many cellular and physiological processes and are essential components of plant nutrition. Therefore, the uptake of cations and their redistribution must be precisely controlled. Vacuolar antiporters are important elements in mediating the intracellular sequestration of these cations. CAXs (for CAtion eXchanger) are members of a multigene family and appear to predominately reside on vacuoles. Defining CAX regulation and substrate specificity have been aided by utilizing yeast as an experimental tool. Studies in plants suggest CAXs regulate apoplastic Ca2+ levels in order to optimize cell wall expansion, photosynthesis, transpiration and plant productivity. CAX studies provide the basis for making designer transporters that have been used to develop nutrient enhanced crops and plants for remediating toxic soils. In my second study, I have characterized and defined autoinhibitory domain of Arabidopsis CAX3. Several CAX transporters, including CAX1, appear to contain an approximately 40 amino acid N-terminal regulatory regions (NRR) that modulates transport through N-terminal autoinhibition. Deletion of the NRR from several CAXs (sCAX) enhances function in plant and yeast expression assays; however, to date, there are no functional assays for CAX3. In this report, we create a series of truncations in the CAX3 NRR and demonstrate activation of CAX3 in both yeast and plants by truncating a large portion of the NRR. Experiments on endomembrane-enriched vesicles isolated from yeast expressing activated CAX3 demonstrate that the gene encodes Ca2+/H+ exchange with properties distinct from CAX1. These studies demonstrate shared and unique aspects of CAX1 and CAX3 transport and regulation. My third study is to express and purify CAX proteins for X-ray crystallographic analysis. In this study, I initiated crystallization of vacuolar membrane localized CAX protein from eukaryotes. Membrane proteins continue to be challenging targets for structural biology because of their hydrophobic nature. We have demonstrated here that eukaryotic Ca2+/H+ exchanger can be successfully expressed in E. coli based expression system. Collectively, our findings suggest that CAX protein can be successfully expressed, detergent solublized and purified from E. coli with a yield sufficient for functional and structural studies.

xiv, 81 p. : ill. (some col.) A print copy of this thesis is available through the UO Libraries. Search the library catalog for the location and call number. / Protein-protein interaction networks translate environmental inputs into specific physiological outputs. The signaling proteins in these networks require regulatory mechanisms to ensure proper molecular function. Two common regulatory features of signaling proteins are autoinhibition and ultrasensitivity. Autoinhibition locks the protein in an inactive state through cis interactions with a regulatory module until it is activated by a specific input signal. Ultrasensitivity, defined as steep activation after a threshold, allows cells to convert graded inputs into more switch-like outputs and can lead to complex decision making behaviors such as bistability. Although these mechanisms are common features of signaling proteins, their molecular origins are poorly understood. I used the Drosophila Pins protein, a regulator of spindle positioning in neuroblast cells, as a model to study the molecular origin and function of autoinhibition and ultrasensitivity. Pins and its binding partners. Gαi and Mud, form a signaling pathway required for coordinating spindle positioning with cellular polarity in Drosophila neuroblasts. I found Pins switches from an autoinhibited to an activate state by modular allostery. Gαi binding to the third of three GoLoco (GL) domains allows Pins to interact with the microtubule binding protein Mud. The GL3 region is required for autoinhibitoon, as amino acids upstream and within GL3 constitute this regulatory behavior. This autoinhibitory module is conserved in LGN, the mammalian Pins orthologue. I also demonstrated that Gαi activation of Pins is ultrasensitive. A Pins protein containing inactivating point mutations to GLs l and 2 exhibits non-ultrasensitive (graded) activation. Ultrasensitivity is required for Pins function in vivo as the graded Pins mutant fails to robustly orient the mitotic spindle. I considered two models for the source of ultrasensitivity in this pathway: cooperative or "decoy" Gai binding. I found ultrasensitivity arises from a decoy mechanism in which GLs 1 and 2 compete with the activating GL3 for the input, Gai. These findings suggest that molecular ultrasensitivity can be generated without cooperativity. This decoy mechanism is relatively simple, suggesting ultrasensitive responses can be evolved by the inclusion of domain repeats, a common feature observed in signaling proteins. This dissertation includes previously published and unpublished co-authored material. / Committee in charge: Tom Stevens, Chairperson, Chemistry; Kenneth Prehoda, Member, Chemistry; Christopher Doe, Member, Biology; Peter von Hippel, Member, Chemistry; Karen Guillemin, Outside Member, Biology

DNA-Restriktions und -Modifikationssysteme sind in Prokaryoten weit verbreitet und stellen einen wirksamen Schutz gegen das Eindringen mobiler genetischer Elemente dar. Sie kodieren für eine Restriktionsendonuklease (REase) und eine DNA-Methyltransferase (MTase) gleicher Nukleotidsequenz Spezifität. Die MTase methyliert die zelluläre DNA und schützt sie durch diesen epigenetischen Marker vor der Wirkung der REase. Die REase verhindert die Aufnahme fremder, unmethylierter DNA durch sequenzspezifische Spaltung. EcoRII ist eine REase, die für die effiziente DNA-Spaltung mindestens zwei Kopien ihrer Erkennungssequenz benötigt. Untersuchungen der EcoRII-Struktur und -Funktion offenbarten, dass das Protein aus zwei stabilen Domänen aufgebaut ist, wobei die N-terminale Domäne wie ein Repressor die C-terminale Domäne sterisch blockiert und deren katalytische Aktivität verhindert. Dieser als Autoinhibition bezeichnete und von eukaryotischen Proteinen gut bekannter Regulationsmechanismus wurde erstmals für eine REase vorgeschlagen. In dieser Arbeit konnten wir die Regulation der EcoRII-Enzymaktivität durch Autoinhibition auf molekularer Ebene beweisen. Wir identifizierten ß-Strang 1 (B1: 18YFVYIKR24) und a-Helix 2 (H2: 26SANDT30) als essenzielle inhibitorische Elemente der N-terminalen Domäne des EcoRII-Moleküls. Die Deletion von B1 oder H2 führte zu einer vollständigen Aufhebung der Autoinhibition. Darüber hinaus ist es uns gelungen, die 3D-Röntgenkristallstruktur von EcoRII mit 1,9 Å zu lösen und mit Hilfe von Computermodellen neue Interaktionen des Enzyms mit der DNA „minor groove“ zu beschreiben sowie eine Mg2+-Bindungstasche zu charakterisieren. Die Untersuchung der EcoRII-MTase durch limitierte Proteolyse zeigte, dass das Enzym in Abhängigkeit von der DNA-Sequenz und von seinen Kofaktoren, DNA auf unterschiedliche Weise binden kann. Kristallisierungsversuche der EcoRII-MTase in Anwesenheit der hemi-methylierten DNA-Erkennungssequenz ergaben erste diffraktierende Kristalle, deren Qualität optimiert werden muss und zur Strukturlösung führen soll. / Restriction and modification systems are wide spread among prokaryotes and pre-sent an efficient protection against invasion of mobile genetic elements. In general, they code for a restriction endonuclease (REase) and a DNA-methyltransferase (MTase) of the same DNA specificity. The MTase methylates the cellular DNA and by this epigenetic marker protects it against the action of the REase. The REase pre-vents the entry of foreign unmethylated DNA by site-specific cleavage. EcoRII is an REase which needs at least two copies of the recognition sequence for efficient cleavage. Investigations of the EcoRII structure and function revealed that the pro-tein is composed of two stable domains: the N-terminal domain acts as a repressor by sterically blocking the C-terminal domain and thereby inhibiting its catalytic activity. This regulatory mechanism is known as autoinhibition and has been often described for eukaryotic proteins, but for the first time was proposed for a REase. In this work, we verified the regulation of the EcoRII enzyme activity by autoinhibition at the molecular level. We identified ß-strand 1 (B1: 18YFVYIKR24) and a-helix 2 (H2: 26SANDT30) as essential inhibitory elements of the N-terminal domain. Deletion of B1 or H2 caused a complete abolishment of the autoinhibition. Fur-thermore, we were able to solve the 3D-X-ray crystal structure of EcoRII at 1.9 Å. Based on computer modelling we discovered new interactions between EcoRII and the DNA minor groove and defined the position of the Mg2+ binding pocket. Investigations of the EcoRII MTase by limited proteolysis showed that the enzyme binds DNA depending on DNA sequence and cofactors in different manners. Crystallography experiments with EcoRII MTase in the presence of hemimethylated recognition site DNA showed for the first time diffracting crystals which need further optimisation to create high quality crystals which allow structure solution.

Phosphoinositide-dependent protein kinase-1 (PDK1) plays an integral role in signaling cellular growth and proliferation, one that's dependent on its ability to autophosphorylate Ser-241 in its T-loop. This process appears to have a strict requirement for its C-terminal pleckstrin homology (PH) domain. Thus, the overall objective of this work was to determine the mechanism by which the PH domain induces an active kinase conformation in unphosphorylated PDK1, capable of Ser-241 autophosphorylation. First, computational modeling and protein cross linking studies were combined with site-directed mutagenesis and kinetic assays in order to provide initial assessment of how the PH domain scaffolds Ser-241 autophosphorylation. A significant number of contacts were identified between the enigmatic "N-bud" region of the PH domain and the kinase domain. Specifically, these studies implicated Glu-432 and Glu-453 of the N-bud region of the PH domain that bind and serve as mimics of the phosphorylated Ser-241 in the T-loop and the phosphorylated C-terminal tail of PDK1 substrates, respectively. Next, a novel method for protein trans-splicing of the regulatory and catalytic kinase domains of PDK1 was developed. The method utilizes the N- and C-terminal split inteins of the gene dnaE from Nostoc punctiforme [(N)NpuDnaE] and Synechocystis sp. strain PCC6803 [(C)SspDnaE], respectively. The cross-reacting KINASE(AEY)-(N)NpuDnaE-His6 and GST-His6-(C)SspDnaE-(CMN)PH fusion constructs generated full length spliced-PDK1 with kobs = (2.8 +- 0.3) x 10-5 s-1. Finally, NMR was used to further characterize the structural and dynamical properties of the PH domain in both its isolated form and in full length PDK1. Whereas, it was not possible to obtain chemical shift assignments of any backbone or side chain nuclear resonances, methods were optimized for 2H,13C,15N-isotopic labeling of the recombinant PH domain. Furthermore, the protein trans-splicing method was significantly improved and utilized for segmental isotopic labeling of the PH domain in full length PDK1. These new findings and developments may provide specific insight and technological improvements towards future studies aimed to better understand and target autoinhibited conformations of PDK1 for translational purposes.

Cyclic nucleotides such as cAMP and cGMP serve as intracellular second messengers in diverse signaling pathways that control a wide range of cellular functions. Such pathways are regulated by key cyclic nucleotide receptor proteins including protein kinase A (PKA), the exchange protein directly activated by cAMP (EPAC), the hyperpolarization-activated cyclic-nucleotide-modulated (HCN) ion channels, and protein kinase G (PKG), and malfunction of these proteins has been linked to a number of pathologies. While it is known that cyclic nucleotide binding to these proteins leads to structural perturbations that promote their activation, the role played by dynamics in auto-inhibition and cyclic-nucleotide-dependent activation is not fully understood. Therefore, in this thesis we examined dynamics within the cyclic-nucleotide receptor proteins EPAC, HCN and PKG, and found that dynamics are critical for allosteric control of activation and/or autoinhibition of all three proteins. In particular, our findings for EPAC and HCN have highlighted dynamics as a key modulator of the entropic and enthalpic components, respectively, of the free-energy landscape for cAMP-dependent allostery, while our findings for PKG have highlighted dynamics as a key determinant of the cGMP-vs.-cAMP selectivity necessary to minimize cross-talk between signaling pathways. Ultimately, we envision that the methods outlined in this thesis will reveal key differences in the regulatory mechanisms of human cyclic nucleotide receptors that can eventually be exploited in the development of novel therapeutics to selectively target a single receptor, and thus treat physiological conditions/diseases linked to malfunction of the target receptor. / Thesis / Doctor of Philosophy (PhD) / In this thesis, we examined cyclic-nucleotide-responsive proteins that regulate key physiological processes, and whose malfunction has been linked to cardiovascular and neurological disorders. In particular, in three such proteins we examined dynamics, whose role in cyclic-nucleotide-responsive function is not fully understood. We found that cyclic-nucleotide-dependent variations in dynamics play a critical role in the function of these proteins, with the results for each protein highlighting a different role played by dynamics. Ultimately, we envision that the methods outlined in this thesis will reveal key functional differences among human cyclic-nucleotide-responsive proteins that can eventually lead to the development of novel therapeutics to treat certain diseases such as arrhythmias or epilepsy by selectively targeting a single cyclic-nucleotide-responsive protein.

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