Fragment based Drug Discovery; Design and Validation of a Fragment Library; Computer-based Fragment Screening and Fragment-to-Lead Expansion

In recent years, fragment screening has become a popular approach to identify new lead structures. Fragments are usually defined by the Astex ‘rule of three’ (RO3). Surface Plasmon Resonance (SPR), Nuclear Magnetic Resonance spectroscopy (NMR), biochemical assays and X-ray crystallography are efficient screening techniques to discover prospective fragments as binders. However, these methods need an assembled fragment library. We designed an in-house fragment library, starting from approx. 380,000 commercially available fragments. During library design, we modified the RO3 and we did no strict filtering of physico-chemical properties during fragment enumeration (e.g. twice the number of H-bond acceptors was allowed). The fragments were stepwise reduced to 4,000 compounds. The last step was a visual inspection of the candidates, which lead to a final fragment library of 364 fragments. To validate the quality of the library, we screened it against endothiapepsin. The biochemical screening suggested 55 hits, which were entered into a crystallographic screen. Eleven complex crystal structures were determined, pointing out the remarkably high hit rate of the designed library. HotspotsX is a program which predicts (based on knowledge-based potentials) the probability of a certain atom type at a certain position in the binding pocket of a target enzyme. The eleven crystal structures obtained before were used to validate the program HotspotsX. Due to chemical diversity and the different binding modes of the fragments observed for the library examples we obtained binding through aromatic- , H-bond donor- , acceptor- , doneptor- and hydrophobic interactions. The calculated HotspotsX maps coincide remarkably well with the crystallographically determined fragment positions inside the binding pocket. The program HotspotsX has also been validated with crystal structures of molecular probes like phenol, urea and methylurea. Crystal structures of these molecular probes were determined with different targets. Overall, the experimental hotspot analysis coincided well with the computed contour maps. Thus, the calculated maps by HotspotsX have an excellent predictive power. Based on the binding modes of the molecular probe phenol to the cAMP-dependent protein kinase A (PKA), we started a fragment growing approach. In the latter complex, three phenol molecules are bound. Two are occupying the ATP binding site and one is sitting on top of the glycine-rich loop (G-loop). A virtual screening, using the hinge binding phenol as constraint, suggested a phenol derivative for which a crystal structure could be determined. Starting from this hit, a hotspot analysis was performed. This analysis indicates that growth in the direction of the G-loop, placing an aromatic portion under the G-loop and an acceptor functionality capable to address Lys72 is desired. The first compound of this de novo design had an affinity of 70 µM. In the following first design cycle, we were able to enhance the affinity to 6.5 µM. In the second design cycle an additional amino function was introduced, which did not improve affinity dramatically, but enhanced ligand efficiency to 0.38. In the last cycle, a spacer of one and two methylene groups was introduced and the affinity could be increased to about 110 nM for a diastereomeric mixture of four compounds. The phenol-PKA complex provides a putative allosteric site of PKA. The G-loop in this structure is in a closed state which is stabilized by two H-bonds. This G-loop conformation is probably induced by the phenol molecule sitting on top of the G-loop. Therefore, several molecular dynamics (MD) studies were performed, lacking different phenol molecules, to get insights into the G-loop opening. The MD studies suggest that after removal of the phenol sitting on top of the G-loop some first side chain movements are initiated that can indicate the first steps of the G-loop opening cascade. In a different project, a virtual screening approach was used to find new inhibitors for aldose reductase. A pre-filtered subset of the ZINC database was used as ligand dataset. For the best hit, a series of five compounds was synthesized. Among them one compound displayed an inhibition of 920 nM. The available assays to detect fragment hits are currently not sufficient. The challenges are the low affinity of the fragments and their poor solubility. Therefore, the known thermal shift assay was applied and adapted to detect fragment hits. To validate the method, it was used to characterize variant mutations of EctD. Lastly, a modeling study was used to get ideas about possible binding modes of arachidonic acid derivatives in a K+ ion channel. One predominant binding pose could not be suggested. The study proposes, however, that one arachidonic acid molecule can occupy the inner pore cavity, which is consistent with experimental data

Entrepreneurial financing of micro-small-medium enterprises in Haiti: barriers and proposed solutions

Este estudio busca examinar la esfera empresarial en Hait? con especial atenci?n en aspectos de financiaci?n para aquellos que desean iniciar o ampliar un negocio. Busca comprender los efectos de la falta de educaci?n financiera en las micro, peque?as y medianas empresas (MIPYME) empresarios que evolucionan dentro de la econom?a haitiana. La revisi?n de la literatura discute varios factores contextuales que impactan a los empresarios haitianos, incluido el entorno pol?tico haitiano, el acceso a la financiaci?n a trav?s de la banca tradicional y la microempresa financiaci?n y barreras al emprendimiento. Adem?s, explora resultados como informalidad y analiza las teor?as existentes sobre la reducci?n de la pobreza a trav?s de las IMF (micro finanzas instituciones). Termina con una discusi?n sobre los diversos roles que la di?spora haitiana, la Empresarios haitianos para encontrar estabilidad buscan crear empleos y construir la econom?a haitiana. Esta tesis incluye los resultados de 12 entrevistas cualitativas con expertos en Hait?, finanzas en Hait? o en emprendimiento realizado en un per?odo de un mes MIPYMES locales y miembros de la di?spora haitiana. El objetivo era entender las percepciones de las empresas de financiaci?n empresarial en Hait? para las MIPYMES a trav?s de entrevistas a participantes de diferentes or?genes y realidades en el complejo mundo que es el Hait? moderno. Los resultados sugieren que la educaci?n financiera, el acceso a las finanzas y la informalidad dentro de son elementos de disuasi?n para la escala empresarial en Hait?. Sin embargo, los resultados tambi?n indican que la esfera empresarial en Hait? est? muy da?ada asociaci?n para mejorar las condiciones actuales y conducir al crecimiento sostenible de Hait? econom?a a trav?s de "solopreneurs" que se convertir?an en formas m?s s?lidas de empresarios, si est?n calificados para hacerlo

Synthesis of 5-Hydroxyectoine from Ectoine: Crystal Structure of the Non-Heme Iron(II) and 2-Oxoglutarate-Dependent Dioxygenase EctD

As a response to high osmolality, many microorganisms synthesize various types of compatible solutes. These organic osmolytes aid in offsetting the detrimental effects of low water activity on cell physiology. One of these compatible solutes is ectoine. A sub-group of the ectoine producer's enzymatically convert this tetrahydropyrimidine into a hydroxylated derivative, 5-hydroxyectoine. This compound also functions as an effective osmostress protectant and compatible solute but it possesses properties that differ in several aspects from those of ectoine. The enzyme responsible for ectoine hydroxylation (EctD) is a member of the non-heme iron(II)-containing and 2-oxoglutarate-dependent dioxygenases (EC 1.14.11). These enzymes couple the decarboxylation of 2-oxoglutarate with the formation of a high-energy ferryl-oxo intermediate to catalyze the oxidation of the bound organic substrate. We report here the crystal structure of the ectoine hydroxylase EctD from the moderate halophile Virgibacillus salexigens in complex with Fe3+ at a resolution of 1.85 Å. Like other non-heme iron(II) and 2-oxoglutarate dependent dioxygenases, the core of the EctD structure consists of a double-stranded β-helix forming the main portion of the active-site of the enzyme. The positioning of the iron ligand in the active-site of EctD is mediated by an evolutionarily conserved 2-His-1-carboxylate iron-binding motif. The side chains of the three residues forming this iron-binding site protrude into a deep cavity in the EctD structure that also harbours the 2-oxoglutarate co-substrate-binding site. Database searches revealed a widespread occurrence of EctD-type proteins in members of the Bacteria but only in a single representative of the Archaea, the marine crenarchaeon Nitrosopumilus maritimus. The EctD crystal structure reported here can serve as a template to guide further biochemical and structural studies of this biotechnologically interesting enzyme family

Effects of insulin, sodium and D-glucose on amino acid absorption in the intestine of rats

Amino acid absorption across rat intestine in vitro was inhibited or stimulated by insulin depending on the hormone serosal concentration. The absence of sodium ions from the incubating solution resulted in a significant decrease of L-alanine absorption. However, L-alanine was enhanced in a sodium-free medium by the addition of insulin on the serosal side of the intestine. A sizable decrease in L-alanine and L-lysine absorption was produced by introduction of D-glucose (0.2 % and 2 %) in the Krebs-Ringer\u27s incubating buffer. Nevertheless, the presence of D-glucose did not prevent the stimulatory effect of insulin on amino acid absorptio

Plan of the battle of Waterloo or Mount St. John [cartographic material] : reduced from the large plan of the same battle, made up and published in 1816 /

Map set in text showing English, German, Belgian, Dutch and French positions. Relief shown by hachures.; Also available in an electronic version via the Internet at: http://nla.gov.au/nla.map-rm1383; Library holds three copies. Copies 2 and 3 damaged

WATERLOO (Bélgica). Batallas (1815). 1:13000

Escalas gráficas además en 1/4 de hora de camino, 1/4 de legua de Brabante, una milla inglesa y 1/4 de milla de Alemania. Orientado con flechaRelieve representado por normalesRelación de las posiciones de las tropas indicadas por clave cromáticaTabla de signos convencionales para indicar los avances, ataques, baterias, etc.Acompañado de una hoja explicativ