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      Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions

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          Abstract

          Genomic and epigenomic studies require the precise transfer of microliter volumes among different types of tubes in order to purify DNA, RNA, or protein from biological samples and subsequently perform analyses of DNA methylation, RNA expression, and chromatin modifications on a genome-wide scale. Epigenomic and transcriptional analyses of human blood cells, for example, require separation of purified cell types to avoid confounding contributions of altered cellular proportions, and long-term preservation of these cells requires their isolation and transfer into appropriate freezing media. There are currently no protocols for these cellular isolation procedures on the International Space Station (ISS). Currently human blood samples are either frozen as mixed cell populations (within the CPT collection tubes) with poor yield of viable cells required for cell-type isolations, or returned under ambient conditions, which requires timing with Soyuz missions. Here we evaluate the feasibility of translating terrestrial cell purification techniques to the ISS. Our evaluations were performed in microgravity conditions during parabolic atmospheric flight. The pipetting of open liquids in microgravity was evaluated using analog-blood fluids and several types of pipette hardware. The best-performing pipettors were used to evaluate the pipetting steps required for peripheral blood mononuclear cell (PBMC) isolation following terrestrial density-gradient centrifugation. Evaluation of actual blood products was performed for both the overlay of diluted blood, and the transfer of isolated PBMCs. We also validated magnetic purification of cells. We found that positive-displacement pipettors avoided air bubbles, and the tips allowed the strong surface tension of water, glycerol, and blood to maintain a patent meniscus and withstand robust pipetting in microgravity. These procedures will greatly increase the breadth of research that can be performed on board the ISS, and allow improvised experimentation by astronauts on extraterrestrial missions.

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          Synthesis and use of an asymmetric transfer hydrogenation catalyst based on iron(II) for the synthesis of enantioenriched alcohols and amines

          The catalytic hydrogenation of prochiral ketones and imines is an advantageous approach to the synthesis of enantioenriched alcohols and amines, respectively, which are two classes of compounds that are highly prized in pharmaceutical, fragrance and flavoring chemistry. This hydrogenation reaction is generally carried out using ruthenium-based catalysts. Our group has developed an alternative synthetic route that is based on the environmentally friendlier iron-based catalysis. This protocol describes the three-part synthesis of trans-[amine(imine)diphosphine]chlorocarbonyliron(II) tetrafluoroborate templated by iron salts and starting from commercially available chemicals, which provides the precatalyst for the efficient asymmetric transfer hydrogenation of ketones and imines. The use of the enantiopure (S,S) catalyst to reduce prochiral ketones to the (R)-alcohol in good to excellent yields and enantioenrichment is also detailed, as well as the reduction to the amine in very high yield and enantiopurity of imines substituted at the nitrogen with the N-(diphenylphosphinoyl) group (-P(O)Ph2). Although the best ruthenium catalysts provide alcohols in higher enantiomeric excess (ee) than the iron complex catalyst used in this protocol, they do so on much longer time scales or at higher catalyst loadings. This protocol can be completed in 2 weeks.
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            Author and article information

            Journal
            NPJ Microgravity
            NPJ Microgravity
            NPJ Microgravity
            Nature Publishing Group
            2373-8065
            14 July 2016
            2016
            : 2
            : 16025
            Affiliations
            [1 ]Center for Epigenetics, Johns Hopkins University School of Medicine , Baltimore, MD, USA
            [2 ]Science, Technology and Engineering Group , Wyle, Houston, TX, USA
            [3 ]Astronaut Office, NASA Johnson Space Center , Houston, TX, USA
            [4 ]Department of Anesthesiology, Hospital of the Ludwig-Maximilians-University , Munich, Germany
            [5 ]JES Tech , Houston, TX, USA
            [6 ]Space and Clinical Operations Division, NASA Johnson Space Center , Houston, TX, USA
            [7 ]Biomedical Research and Environmental Sciences Division, NASA Johnson Space Center , Houston, TX, USA
            [8 ]Departments of Medicine, Biomedical Engineering, and Mental Health, Johns Hopkins University Schools of Medicine, Engineering, and Public Health , Baltimore, MD, USA
            Author notes
            [9]

            These authors contributed equally to this work.

            [10]

            Corresponding authors contributed equally to this work.

            L.F.R., K.R., C.S., B.C., and A.P.F. designed the study. Experiments were performed by L.F.R., H.K., K.R., B.C., and A.P.F. L.F.R., H.K. and B.C. wrote the manuscript with input and editing from all authors.

            Author information
            http://orcid.org/0000-0002-2866-9625
            Article
            npjmgrav201625
            10.1038/npjmgrav.2016.25
            5515526
            2ef9f2fd-5bc9-42ed-94c0-d16a2e3f0eae
            Copyright © 2016 The Author(s)

            This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

            History
            : 04 February 2016
            : 08 June 2016
            : 09 June 2016
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