152 research outputs found

    Space Research Projects for the International Space Station

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    Space Italian Dressing Experimental Setup (SIDES) examines the dynamics of fluid segregation between fluids of differing densities. While in space the fluids will not undergo buoyant or convective forces, thus isolating the affects of separation due to density and molecular forces. The experiment will serve as an outreach experiment in addition to gleaning scientific data; mixtures are a topic of study in the 5th grade curriculum. The objective of International Paper Airplanes in Space (IPAS) is to excite children about space research by giving them a chance to take part in it. IPAS includes collecting paper airplanes made by elementary-school students from around the world. The airplanes will be sent to the International Space Station to determine the effects of microgravity on paper airplane flight. The data will be recorded, collected, and then disseminated. Research on the Effects of Microgravity on the BRazil NuT problem (REMBRANT) examines the affects of inertia on granular separation. The experiment includes two to four different bead sizes in one container that will be shaken and recorded to evaluate the ensuing collisions. Because of minimized gravitational effects, the granules will not be subject to buoyant or convective forces

    Space Research Projects for the International Space Station

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    A Temporal Metaphysics for Affective Attitudes

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    This thesis endeavours to achieve two things: first, it exposits a version of presentism, the doctrine that only present concrete entities exist, that is enriched with haecceities, the non- qualitative, essential properties of entities that characterise their essences. I argue that haecceity presentism provides strong responses to problematics traditionally faced by presentism (providing ontology for singular propositions, truthmaking, and cross-temporal relations and causation) without violating any of presentism’s strictures. I also distinguish my version of haecceity presentism from other versions, and argue my version is the strongest. Second, I deploy haecceities to mount novel lines of attack on critical elements of the B- theory: eternalism, perdurance, and stage theory. These attacks say that each of these tenseless theories of time and persistence cannot adequately rationalise and vindicate the importance of emotions in our lives, and how they contribute to crucially important projects such as rehabilitation. Further, these tenseless theories generate critical problems with some of our moral practices, such as blame, as well as generating radically alienating consequences for it. Consequently, tenseless theorists should either acknowledge the importance of emotions and reject their theories, or be honest and transparent in accepting that they cannot rationalise or vindicate emotions

    Structure of the γ-D-glutamyl-L-diamino acid endopeptidase YkfC from Bacillus cereus in complex with L-Ala-γ-D-Glu: insights into substrate recognition by NlpC/P60 cysteine peptidases.

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    Dipeptidyl-peptidase VI from Bacillus sphaericus and YkfC from Bacillus subtilis have both previously been characterized as highly specific γ-D-glutamyl-L-diamino acid endopeptidases. The crystal structure of a YkfC ortholog from Bacillus cereus (BcYkfC) at 1.8 Å resolution revealed that it contains two N-terminal bacterial SH3 (SH3b) domains in addition to the C-terminal catalytic NlpC/P60 domain that is ubiquitous in the very large family of cell-wall-related cysteine peptidases. A bound reaction product (L-Ala-γ-D-Glu) enabled the identification of conserved sequence and structural signatures for recognition of L-Ala and γ-D-Glu and, therefore, provides a clear framework for understanding the substrate specificity observed in dipeptidyl-peptidase VI, YkfC and other NlpC/P60 domains in general. The first SH3b domain plays an important role in defining substrate specificity by contributing to the formation of the active site, such that only murein peptides with a free N-terminal alanine are allowed. A conserved tyrosine in the SH3b domain of the YkfC subfamily is correlated with the presence of a conserved acidic residue in the NlpC/P60 domain and both residues interact with the free amine group of the alanine. This structural feature allows the definition of a subfamily of NlpC/P60 enzymes with the same N-terminal substrate requirements, including a previously characterized cyanobacterial L-alanine-γ-D-glutamate endopeptidase that contains the two key components (an NlpC/P60 domain attached to an SH3b domain) for assembly of a YkfC-like active site

    The structure of BVU2987 from Bacteroides vulgatus reveals a superfamily of bacterial periplasmic proteins with possible inhibitory function.

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    Proteins that contain the DUF2874 domain constitute a new Pfam family PF11396. Members of this family have predominantly been identified in microbes found in the human gut and oral cavity. The crystal structure of one member of this family, BVU2987 from Bacteroides vulgatus, has been determined, revealing a β-lactamase inhibitor protein-like structure with a tandem repeat of domains. Sequence analysis and structural comparisons reveal that BVU2987 and other DUF2874 proteins are related to β-lactamase inhibitor protein, PepSY and SmpA_OmlA proteins and hence are likely to function as inhibitory proteins

    The Free Fatty Acid-Binding Pocket is a Conserved Hallmark in Pathogenic β-Coronavirus Spike Proteins from SARS-CoV to Omicron

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    As coronavirus disease 2019 (COVID-19) persists, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) emerge, accumulating spike (S) glycoprotein mutations. S receptor binding domain (RBD) comprises a free fatty acid (FFA)–binding pocket. FFA binding stabilizes a locked S conformation, interfering with virus infectivity. We provide evidence that the pocket is conserved in pathogenic β-coronaviruses (β-CoVs) infecting humans. SARS-CoV, MERS-CoV, SARS-CoV-2, and VOCs bind the essential FFA linoleic acid (LA), while binding is abolished by one mutation in common cold–causing HCoV-HKU1. In the SARS-CoV S structure, LA stabilizes the locked conformation, while the open, infectious conformation is devoid of LA. Electron tomography of SARS-CoV-2–infected cells reveals that LA treatment inhibits viral replication, resulting in fewer deformed virions. Our results establish FFA binding as a hallmark of pathogenic β-CoV infection and replication, setting the stage for FFA-based antiviral strategies to overcome COVID-19
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