Ferrari, Ana Lya Moya, Piculo dos Santos, Aline Darc, Bertolaccini, Guilherme da Silva, Medola, Fausto Orsi, and Sandnes, Frode Eika
Ferrari, A.L.M., Piculo dos Santos, A.D., Bertolaccini, G.S., Medola, F.O. & Sandnes, F.E. (2020). Evaluation of orthosis rapid prototyping during the design process: Analysis of verification models. In: M. Di Nicolantonio, E. Rossi & T. Alexander (Eds.), Advances in additive manufacturing, modeling systems and 3D prototyping: Proceedings of the AHFE 2019 International Conference on Additive Manufacturing, Modeling Systems and 3D Prototyping, Cham: Springer (pp. 298-307)
Usó, Vanessa Ghiraldeli, Sandnes, Frode Eika, and Medola, Fausto Orsi
Usó, V.G., Sandnes, F.E. & Medola, F.O. (2020). Using virtual reality and rapid prototyping to co-create together with hospitalized children. In: M. Di Nicolantonio, E. Rossi & T. Alexander (Eds.). Advances in additive manufacturing, modeling systems and 3D prototyping: Proceedings of the AHFE 2019 International Conference on Additive Manufacturing, Modeling Systems and 3D Prototyping, 2020 (pp. 279-288) Cham: Springer
Conservation Biology. Dec 2019, Vol. 33 Issue 6, p1448, 3 p.
***** No abstract is available for this article. Article Note: Article impact statement: Web-application development frameworks enable the creation of decision-support tool prototypes for actionable conservation science. CAPTION(S): Table 1. List of web-application development frameworks that might be useful for conservation scientists. Byline: Denis Valle, Kok Ben Toh, Justin Millar
Dopp, Jared Lynn, Rothstein, Samuel Michael, Mansell, Thomas Joseph, and Reuel, Nigel Forest
Biotechnology and Bioengineering. March 2019, Vol. 116 Issue 3, p667, 10 p.
Rapid prototyping, Proteins, Genetic research, Mail-order industry, Fluorescence, Protein biosynthesis, Genes, Escherichia coli, and DNA synthesis
Byline: Jared Lynn Dopp, Samuel Michael Rothstein, Thomas Joseph Mansell,Nigel Forest Reuel Keywords: cell-free protein synthesis; linear template; rolling circle amplification Abstract In this study, we present a minimal template design and accompanying methods to produce assayable quantities of custom sequence proteins within 24hr from receipt of inexpensive gene fragments from a DNA synthesis vendor. This is done without the conventional steps of plasmid cloning or cell-based amplification and expression. Instead the linear template is PCR amplified, circularized, and isothermally amplified using a rolling circle polymerase. The resulting template can be used directly with cost-optimized, scalably-manufactured Escherichia coli extract and minimal supplement reagents to perform cell-free protein synthesis (CFPS) of the template protein. We demonstrate the utility of this template design and 24hr process with seven fluorescent proteins (sfGFP, mVenus, mCherry, and four GFP variants), three enzymes (chloramphenicol acetyltransferase, a chitinase catalytic domain, and native subtilisin), a capture protein (anti-GFP nanobody), and 2 antimicrobial peptides (BP100 and CA(1-7)M(2-9)). We detected each of these directly from the CFPS reaction using colorimetric, fluorogenic, and growth assays. Of especial note, the GFP variant sequences were found from genomic screening data and had not been expressed or characterized before, thus demonstrating the utility of this approach for phenotype characterization of sequenced libraries. We also demonstrate that the rolling circle amplified version of the linear template exhibits expression similar to that of a complete plasmid when expressing sfGFP in the CFPS reaction. We evaluate the cost of this approach to be $61/mg sfGFP for a 4hr reaction. We also detail limitations of this approach and strategies to overcome these, namely proteins with posttranslational modifications. CAPTION(S): Supplementary information