abstract: The physiological phenomenon of sensing temperature is detected by transient receptor (TRP) ion channels, which are pore forming proteins that reside in the membrane bilayer. The cold and hot sensing TRP channels named TRPV1 and TRPM8 respectively, can be modulated by diverse stimuli and are finely tuned by proteins and lipids. PIRT (phosphoinositide interacting regulator of TRP channels) is a small membrane protein that modifies TRPV1 responses to heat and TRPM8 responses to cold. In this dissertation, the first direct measurements between PIRT and TRPM8 are quantified with nuclear magnetic resonance and microscale thermophoresis. Using Rosetta computational biology, TRPM8 is modeled with a regulatory, and functionally essential, lipid named PIP2. Furthermore, a PIRT ligand screen identified several novel small molecular binders for PIRT as well a protein named calmodulin. The ligand screening results implicate PIRT in diverse physiological functions. Additionally, sparse NMR data and state of the art Rosetta protocols were used to experimentally guide PIRT structure predictions. Finally, the mechanism of thermosensing from the evolutionarily conserved sensing domain of TRPV1 was investigated using NMR. The body of work presented herein advances the understanding of thermosensing and TRP channel function with TRP channel regulatory implications for PIRT. / Dissertation/Thesis / Doctoral Dissertation Biochemistry 2018

Wu, Feng. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2010. / Includes bibliographical references (leaves 38-44). / Abstracts in English and Chinese. / Title Page --- p.i / Thesis Committee --- p.ii / Acknowledgment --- p.iv / Table of Contents --- p.v / List of Figures --- p.vii / List of Abbreviations and Symbols --- p.xi / Abstract (English version) --- p.xii / Abstract (Chinese version) --- p.xiii / Chapter 1 --- Introduction --- p.1 / Chapter 1.1 --- Significance of DNA CCTG repeats --- p.1 / Chapter 1.2 --- Objectives of this work --- p.2 / Chapter 1.3 --- DNA structure --- p.3 / Chapter 2 --- Materials and Methods --- p.5 / Chapter 2.1 --- Sample design --- p.5 / Chapter 2.2 --- Sample preparation --- p.5 / Chapter 2.3 --- NMR spectroscopy --- p.6 / Chapter 2.4 --- Resonance assignment --- p.7 / Chapter 3 --- NMR Structural Studies of (CCTG)3 --- p.9 / Chapter 3.1 --- Overview --- p.9 / Chapter 3.2 --- NMR resonance assignments --- p.9 / Chapter 3.3 --- Formation of two-residue CT-loop in the middle repeat of (CCTG)3 --- p.12 / Chapter 3.4 --- C-bulge and T.T mispair in (CCTG)3 hairpin stem region --- p.13 / Chapter 3.5 --- Summary --- p.15 / Chapter 4 --- NMR Structural Studies of (CCTG)4 --- p.16 / Chapter 4.1 --- Overview --- p.16 / Chapter 4.2 --- Conformational exchange in (CCTG)4 --- p.16 / Chapter 4.3 --- Formation of two-residue CT-loops in different repeats of (CCTG)4 --- p.17 / Chapter 4.4 --- Mutational studies of (CCTG)4 --- p.19 / Chapter 4.4.1 --- Mutational studies on the 1st repeat of (CCTG)4: (CCTG)4-C2T --- p.19 / Chapter 4.4.2 --- Mutational studies on the 2nd repeat of (CCTG)4：(CCTG)4-C6T --- p.21 / Chapter 4.4.3 --- Mutational studies on the 3rd repeat of (CCTG)4：(CCTG)4-C 10T --- p.26 / Chapter 4.4.4 --- Mutational studies on the 4th repeat of (CCTG)4: (CCTG)4-C14T --- p.28 / Chapter 4.5 --- Summary --- p.33 / Chapter 5 --- Conclusions and Future Works --- p.35 / References --- p.38

Avaliou-se o uso da RMN em baixa resolução na análise da qualidade interna de frutas intactas, como banana ouro e uva itália, que são frutas climatéricas, que continuam amadurecendo após a colheita e não-climatéricas, respectivamente. As análises das bananas foram realizadas com a seqüência de pulsos CPMG (Carr-Purcell-Meibom-Gill), que gera um sinal dependente do tempo de relaxação transversal (T2). Demonstrou-se que a banana apresenta a água distribuída em três ambientes, vacúolo, citoplasma e parede celular, que tem T2 de 0,5, 0,1 e 0,01s respectivamente. Esses sinais têm intensidade relativa de 0,8; 0,15 e 0,05s respectivamente. Observou-se que o T2 de todos esses componentes aumentam com o amadurecimento de banana. Estudou-se também o efeito de compressão e congelamento nas bananas ouro e observou-se que a intensidade do T2 mais longo decresce em os ambos os casos. As análises das uvas foram realizadas com as seqüências de pulsos CPMG, Inversão-Recuperação (IR), que mede o tempo de relaxação longitudinal (T1) e com a seqüência de pulsos de precessão livre de onda continua (CWFP), que gera um sinal que depende tanto de T1 quanto T2. Como a uva não amadurece após a colheita essas análises foram usados para avaliar a correlação com os parâmetros de qualidade interna como brix, pH, firmeza e umidade. Os dados de RMN das uvas foram analisados com métodos quimiométricos como análises de componentes principais e regressão por mínimos quadrados parciais e demonstraram que tem alta correlação com brix e umidade e pouca ou nenhuma correlação com pH e firmeza. / The internal quality of fresh gold banana and grape was analyzed by Low resolution NMR. The banana analysis had been performed with CPMG (Carr-Purcell-Meibom-Gill) pulse sequence, that generates a decaying signal, dependent of the transverse relaxation time (T2). The results show that water in banana are distributed in three environments, vacuole, cytoplasm and cellular wall, with T2 of 0,5, 0.1 and 0,01s respectively. The relative intensity of signals are 0,8; 0,15 and 0,05, respectively. The T2 increases with banana ripeness. The effect of compression and freezing in the bananas was also studied by CPMG. The results show that the intensity of the longest T2 decreases in the both the cases. The grapes had been analyzed with the pulse sequences CPMG, Inversion-Recovery (IR), which measures the longitudinal relaxation time (T1) and continuous wave free precession (CWFP), that depends on T1 and T2. As the grape does not ripen after harvesting these analyses had been used to evaluate the correlation with the internal quality parameters such as brix, pH, firmness and moisture. The NMR data had been analyzed with chemometric methods such as principal component analysis (PCA) and partial least square regression (PLS) and show high correlation with brix and moisture and almost no correlation with pH and firmness.

Este trabalho descreve o desenvolvimento e a construção de um gerador de pulsos de 8 canais, com interface para controle externo por microcomputador. O gerador possui 16 passos programáveis definindo a largura do pulso entre 200 ns e 10 segundos. Permite também a repetição automática de um intervalo selecionado. O microcomputador tem controle total do gerador de pulsos, incluindo programação de memórias e execução e interrupção de sequências de pulsos. Este gerador foi construído para ser usado em experiências de Ressonância Magnética Nuclear Pulsada, no controle de portas de RF e sistema de detecção / This work describes the development and construction of a 8 channel pulse generator with interface for external microcomputer control. The generator has 16 programmable steps defining pulse widths between 200 nsec and 10 seconds, with 100 nsec resolution. Automatic repeat of a selected step range is also provided. The microcomputer has full control of the pulse generator including programing of memories, execution and interruption of pulse sequences. The generator was built to be used in Pulsed Nuclear Magnetic Resonance experiments to control the high Power RF gate and the detection system

Novas abordagens terapêuticas vêm sendo introduzidas para doenças musculares genéticas como distrofias musculares e miopatias congênitas, distúrbios que permanecem sem cura até o momento. Estes recentes avanços motivaram um interesse renovado e crescente por métodos não invasivos para a caracterização e monitoramento do músculo afetado, particularmente durante e após intervenções terapêuticas. Neste contexto, modelos animais são essenciais para uma melhor compreensão dos mecanismos das doenças e para testar novas terapias. Recentemente, avanços significativos na avaliação não invasiva de modelos murinos para doenças musculares genéticas foram alcançados. Entretanto, diversas linhagens de camundongos ainda não foram caracterizadas de maneira não invasiva, e ainda é necessário o desenvolvimento de métodos sensíveis para a identificação precoce de alterações sutis no músculo de camundongos afetados. A proposta desta tese é aplicar técnicas não invasivas inovadoras no estudo do músculo de modelos murinos para doenças musculares genéticas com fenótipos variados. Três modelos murinos para distrofias musculares (mdx, Largemyd, mdx/ Largemyd) e um modelo murino para miopatia congênita (KI-Dnm2R465W) foram estudados com métodos de Ressonância Magnética Nuclear (RMN). Duas linhagens distróficas (Largemyd, mdx/ Largemyd) e camundongos normais após injúria foram estudados através de micro-Tomografia Computadorizada (micro-CT). Em RMN, todas as linhagens de camundongos afetados apresentaram aumento de T2 muscular, o que foi relacionado a diversas anomalias na análise histológica, como necrose e inflamação, mas também a conjuntos de fibras em regeneração ou a fibras com citoarquitetura alterada. A combinação de RMN com análise de textura permitiu a identificação não ambígua de todas as linhagens distróficas, sendo que apenas a comparação dos valores de T2 muscular não permitiu esta diferenciação. Camundongos mdx mostraram alterações funcionais e morfológicas na rede vascular do músculo. Estudo piloto em camundongos KI-Dnm2R465W revelou tendências de comprometimento da função muscular. Por fim, imagens de micro-CT não permitiram a detecção de diferenças na composição muscular em camundongos distróficos. Este conjunto de resultados não apenas enriquece o painel de modelos murinos para doenças musculares genéticas caracterizados de maneira não invasiva, mas também demonstra um certo grau de especificidade nas anomalias observadas nas imagens, como revelado pela análise de textura. Estes resultados também mostraram que métodos não invasivos de RMN podem ser suficientemente sensíveis para identificar alterações sutis no fenótipo muscular murino, mesmo em estágios precoces. Esta tese foi desenvolvida sob acordo de co-tutela internacional entre a França e o Brasil, e compreendeu uma importante transferência de conhecimento, com os primeiros estudos não invasivos de músculo murino realizados no Brasil. / Novel therapeutic approaches are being introduced for genetic muscle diseases such as muscle dystrophies and congenital myopathies, all of them having remained without cure so far. These recent developments have motivated a renewed and augmented interest in non-invasive methods for muscle characterization and monitoring, particularly during and after therapeutic intervention. In this context, animal models are essential to better understand the disease mechanisms and to test new therapies. Recently, significant advances in the non-invasive evaluation of mouse models for genetic muscle diseases have been achieved. Nevertheless, there were still several mouse strains not characterized non-invasively, and it was necessary to develop sensitive methods to identify subtle alterations in the murine affected muscle. The purpose of this thesis was to apply non-invasive techniques in the study of murine models for genetic muscle diseases with variable phenotypes. Three mouse models for muscle dystrophy (mdx, Largemyd, mdx/ Largemyd) and one mouse model for congenital myopathy (KI-Dnm2R465W) were studied with Nuclear Magnetic Resonance (NMR) methods. Two dystrophic strains (Largemyd, mdx/ Largemyd) and normal mice after injury were studied through micro-Computed Tomography (micro-CT). On NMR, all affected mouse strains presented increased muscle T2, which could be related to variable features in the histological evaluation, including necrosis and inflammation, but also to clusters of fibers under regeneration or with altered cytoarchitecture. The combination of NMR and texture analyses allowed the unambiguous differential identification of all the dystrophic strains, although it was not feasible when comparing the muscle T2 measurements only. Mdx mice showed functional and morphological alterations of vascular network. In the KI-Dnm2R465W mice, a pilot study revealed tendencies of functional impairment. Finally, micro-CT images were unable to detect differences in muscle´s content in dystrophic mice. Altogether, these results not only increased the number of murine models for genetic muscle diseases non-invasively characterized, it also demonstrated some degree of specificity of the imaging anomalies, as revealed by texture analysis. It also showed that non-invasive NMR methods can be sensitive enough to identify subtle alterations in murine muscle phenotype, even in early stages. This thesis was developed under an international joint supervision between France and Brazil, and comprised an important transfer of technology, with the first non-invasive studies of murine muscles performed in Brazil.

Intrinsically disordered proteins (IDPs) do not form stable tertiary structures like their ordered partners. They exist as heterogeneous ensembles that fluctuate over a time scale. Intrinsically disordered regions and proteins are found across different phyla and exert crucial biological functions. They exhibit transient secondary structures in their free state and become folded upon binding to their protein partners via a mechanism called coupled folding and binding. Some IDPs form alpha helices when bound to their protein partners. We observed a set of cancer associated IDPs where the helical binding segments of IDPs are flanked by prolines on both the sides. Helix-breaking prolines are frequently found in IDPs flanking the binding segment and are evolutionarily conserved across phyla. Two studies have shown that helix flanking prolines modulate the function of IDPs by regulating the levels of disorder in their free state and in turn regulating the binding affinities to their partners. We aimed to study if this is a common phenomenon in IDPs that exhibit similar pattern in the conservation of helix flanking prolines. We chose to test the hypothesis in c-Myb-KIX : IDP-target system in which the disordered protein exhibits high residual helicity levels in its free state. c-Myb is a hematopoietic regulator that plays a crucial role in cancer by binding to the KIX domain of CBP. Studying the functional regulation of c-Myb by modulating the disorder levels in c-Myb and in IDPs in general provides a better understanding of the way IDPs function and can be used in therapeutic strategies as IDPs are known to be involved in regulating various cellular processes and diseases. To study the effect of conserved helix flanking prolines on the residual helicity levels of c-Myb and its binding affinity to the KIX domain of CBP, we mutated the prolines to alanines. Mutating prolines to alanines increased the helicity levels of c-Myb in its free state. This small increase in the helicity levels of a highly helical c-Myb showed almost no effect on the binding affinity between cMyb and KIX. We hypothesized that there is a helical threshold for coupled folding and binding beyond which helicity levels of the free state IDP have no effect on its binding to their ordered protein partner. To test this hypothesis, we mutated solvent exposed amino acid residues in c-Myb that reduce its overall helicity and studied its effect on the binding affinity between c-Myb and KIX. Over a broad range of reduction in helicity levels of the free state did not show an effect on the binding affinity but beyond a certain level, decrease in helicity levels showed pronounced effects on the binding affinity between c-Myb and KIX.

Abstract not available

Thesis (Ph. D.)--Ohio State University, 2007. / Title from first page of PDF file. Includes bibliographical references (p. 157-170).

Thesis (Ph.D)--Technische Universiteit Eindhoven, 2005. / Title from document title page. Title from title screen (viewed on Dec. 6, 2007). Includes bibliographical references. Available in PDF format via the World Wide Web.

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