Evaluation of solar cells and arrays for potential solar power satellite applications

Proposed solar array designs and manufacturing methods are evaluated to identify options which show the greatest promise of leading up to the develpment of a cost-effective SPS solar cell array design. The key program elements which have to be accomplished as part of an SPS solar cell array development program are defined. The issues focussed on are: (1) definition of one or more designs of a candidate SPS solar array module, using results from current system studies; (2) development of the necessary manufacturing requirements for the candidate SPS solar cell arrays and an assessment of the market size, timing, and industry infrastructure needed to produce the arrays for the SPS program; (3) evaluation of current DOE, NASA and DOD photovoltaic programs to determine the impacts of recent advances in solar cell materials, array designs and manufacturing technology on the candidate SPS solar cell arrays; and (4) definition of key program elements for the development of the most promising solar cell arrays for the SPS program

Proceedings, MSVSCC 2018

Proceedings of the 12th Annual Modeling, Simulation & Visualization Student Capstone Conference held on April 19, 2018 at VMASC in Suffolk, Virginia. 155 pp

The NASA SBIR product catalog

The purpose of this catalog is to assist small business firms in making the community aware of products emerging from their efforts in the Small Business Innovation Research (SBIR) program. It contains descriptions of some products that have advanced into Phase 3 and others that are identified as prospective products. Both lists of products in this catalog are based on information supplied by NASA SBIR contractors in responding to an invitation to be represented in this document. Generally, all products suggested by the small firms were included in order to meet the goals of information exchange for SBIR results. Of the 444 SBIR contractors NASA queried, 137 provided information on 219 products. The catalog presents the product information in the technology areas listed in the table of contents. Within each area, the products are listed in alphabetical order by product name and are given identifying numbers. Also included is an alphabetical listing of the companies that have products described. This listing cross-references the product list and provides information on the business activity of each firm. In addition, there are three indexes: one a list of firms by states, one that lists the products according to NASA Centers that managed the SBIR projects, and one that lists the products by the relevant Technical Topics utilized in NASA's annual program solicitation under which each SBIR project was selected

Identification of Messenger Molecule Between Mammalian and Bacterial Cells

The rapid escalation of the antibiotic resistance crisis has brought attention to the decline in efficiency of antibiotics which have long been a cornerstone of modern medicine. This project aims to provide novel drug targets for the creation of anti-infective immunotherapies that can treat drug-resistant infections. The identification of said drug target(s) (Molecule X) will allow for the development of an antibody based drug that will neutralize bacterial virulence rather than killing the bacteria. Molecule X will be bound using the protein Sortase A (SrtA). SrtA is a surface protein that controls the virulence of gram positive bacteria by anchoring virulence factors to the cell surface. Molecule X is the signal from mammalian cells that initiates this process. Blocking this signal prevents the activation of bacterial virulence. SrtA is obtained from E. coli cells using affinity chromatography and Molecule X is obtained by collecting the entire mammalian proteome of Chinese Hamster Ovary (CHO) cells. The SrtA and mammalian proteome are mixed together with a crosslinker to covalently bind Molecule X to SrtA. The cross-linked products are purified and analyzed using liquid chromatography with tandem mass spectrometry (LC-MS-MS) and the proteins are identified using a proteomic database. The resulting data is analyzed for Molecule X candidates by grouping the proteins into clusters based on function and subcellular location. The identified clusters are calcium ion dependent, membrane associated, G protein-coupled receptors (GPCR) associated, and adenosine triphosphate (ATP) or guanosine triphosphate (GTP) binding proteins