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Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station

The International Space Station (ISS) National Laboratory is dedicated to studying the effects of space on life and physical systems, and to developing new science and technologies for space exploration. A key aspect of achieving these goals is to operate the ISS National Lab more like an Earth-base...

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Autores principales: Parra, Macarena, Jung, Jimmy, Boone, Travis D., Tran, Luan, Blaber, Elizabeth A., Brown, Mark, Chin, Matthew, Chinn, Tori, Cohen, Jacob, Doebler, Robert, Hoang, Dzung, Hyde, Elizabeth, Lera, Matthew, Luzod, Louie T., Mallinson, Mark, Marcu, Oana, Mohamedaly, Youssef, Ricco, Antonio J., Rubins, Kathleen, Sgarlato, Gregory D., Talavera, Rafael O., Tong, Peter, Uribe, Eddie, Williams, Jeffrey, Wu, Diana, Yousuf, Rukhsana, Richey, Charles S., Schonfeld, Julie, Almeida, Eduardo A. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587110/
https://www.ncbi.nlm.nih.gov/pubmed/28877184
http://dx.doi.org/10.1371/journal.pone.0183480
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author Parra, Macarena
Jung, Jimmy
Boone, Travis D.
Tran, Luan
Blaber, Elizabeth A.
Brown, Mark
Chin, Matthew
Chinn, Tori
Cohen, Jacob
Doebler, Robert
Hoang, Dzung
Hyde, Elizabeth
Lera, Matthew
Luzod, Louie T.
Mallinson, Mark
Marcu, Oana
Mohamedaly, Youssef
Ricco, Antonio J.
Rubins, Kathleen
Sgarlato, Gregory D.
Talavera, Rafael O.
Tong, Peter
Uribe, Eddie
Williams, Jeffrey
Wu, Diana
Yousuf, Rukhsana
Richey, Charles S.
Schonfeld, Julie
Almeida, Eduardo A. C.
author_facet Parra, Macarena
Jung, Jimmy
Boone, Travis D.
Tran, Luan
Blaber, Elizabeth A.
Brown, Mark
Chin, Matthew
Chinn, Tori
Cohen, Jacob
Doebler, Robert
Hoang, Dzung
Hyde, Elizabeth
Lera, Matthew
Luzod, Louie T.
Mallinson, Mark
Marcu, Oana
Mohamedaly, Youssef
Ricco, Antonio J.
Rubins, Kathleen
Sgarlato, Gregory D.
Talavera, Rafael O.
Tong, Peter
Uribe, Eddie
Williams, Jeffrey
Wu, Diana
Yousuf, Rukhsana
Richey, Charles S.
Schonfeld, Julie
Almeida, Eduardo A. C.
author_sort Parra, Macarena
collection PubMed
description The International Space Station (ISS) National Laboratory is dedicated to studying the effects of space on life and physical systems, and to developing new science and technologies for space exploration. A key aspect of achieving these goals is to operate the ISS National Lab more like an Earth-based laboratory, conducting complex end-to-end experimentation, not limited to simple microgravity exposure. Towards that end NASA developed a novel suite of molecular biology laboratory tools, reagents, and methods, named WetLab-2, uniquely designed to operate in microgravity, and to process biological samples for real-time gene expression analysis on-orbit. This includes a novel fluidic RNA Sample Preparation Module and fluid transfer devices, all-in-one lyophilized PCR assays, centrifuge, and a real-time PCR thermal cycler. Here we describe the results from the WetLab-2 validation experiments conducted in microgravity during ISS increment 47/SPX-8. Specifically, quantitative PCR was performed on a concentration series of DNA calibration standards, and Reverse Transcriptase-quantitative PCR was conducted on RNA extracted and purified on-orbit from frozen Escherichia coli and mouse liver tissue. Cycle threshold (Ct) values and PCR efficiencies obtained on-orbit from DNA standards were similar to Earth (1 g) controls. Also, on-orbit multiplex analysis of gene expression from bacterial cells and mammalian tissue RNA samples was successfully conducted in about 3 h, with data transmitted within 2 h of experiment completion. Thermal cycling in microgravity resulted in the trapping of gas bubbles inside septa cap assay tubes, causing small but measurable increases in Ct curve noise and variability. Bubble formation was successfully suppressed in a rapid follow-up on-orbit experiment using standard caps to pressurize PCR tubes and reduce gas release during heating cycles. The WetLab-2 facility now provides a novel operational on-orbit research capability for molecular biology and demonstrates the feasibility of more complex wet bench experiments in the ISS National Lab environment.
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spelling pubmed-55871102017-09-15 Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station Parra, Macarena Jung, Jimmy Boone, Travis D. Tran, Luan Blaber, Elizabeth A. Brown, Mark Chin, Matthew Chinn, Tori Cohen, Jacob Doebler, Robert Hoang, Dzung Hyde, Elizabeth Lera, Matthew Luzod, Louie T. Mallinson, Mark Marcu, Oana Mohamedaly, Youssef Ricco, Antonio J. Rubins, Kathleen Sgarlato, Gregory D. Talavera, Rafael O. Tong, Peter Uribe, Eddie Williams, Jeffrey Wu, Diana Yousuf, Rukhsana Richey, Charles S. Schonfeld, Julie Almeida, Eduardo A. C. PLoS One Research Article The International Space Station (ISS) National Laboratory is dedicated to studying the effects of space on life and physical systems, and to developing new science and technologies for space exploration. A key aspect of achieving these goals is to operate the ISS National Lab more like an Earth-based laboratory, conducting complex end-to-end experimentation, not limited to simple microgravity exposure. Towards that end NASA developed a novel suite of molecular biology laboratory tools, reagents, and methods, named WetLab-2, uniquely designed to operate in microgravity, and to process biological samples for real-time gene expression analysis on-orbit. This includes a novel fluidic RNA Sample Preparation Module and fluid transfer devices, all-in-one lyophilized PCR assays, centrifuge, and a real-time PCR thermal cycler. Here we describe the results from the WetLab-2 validation experiments conducted in microgravity during ISS increment 47/SPX-8. Specifically, quantitative PCR was performed on a concentration series of DNA calibration standards, and Reverse Transcriptase-quantitative PCR was conducted on RNA extracted and purified on-orbit from frozen Escherichia coli and mouse liver tissue. Cycle threshold (Ct) values and PCR efficiencies obtained on-orbit from DNA standards were similar to Earth (1 g) controls. Also, on-orbit multiplex analysis of gene expression from bacterial cells and mammalian tissue RNA samples was successfully conducted in about 3 h, with data transmitted within 2 h of experiment completion. Thermal cycling in microgravity resulted in the trapping of gas bubbles inside septa cap assay tubes, causing small but measurable increases in Ct curve noise and variability. Bubble formation was successfully suppressed in a rapid follow-up on-orbit experiment using standard caps to pressurize PCR tubes and reduce gas release during heating cycles. The WetLab-2 facility now provides a novel operational on-orbit research capability for molecular biology and demonstrates the feasibility of more complex wet bench experiments in the ISS National Lab environment. Public Library of Science 2017-09-06 /pmc/articles/PMC5587110/ /pubmed/28877184 http://dx.doi.org/10.1371/journal.pone.0183480 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Parra, Macarena
Jung, Jimmy
Boone, Travis D.
Tran, Luan
Blaber, Elizabeth A.
Brown, Mark
Chin, Matthew
Chinn, Tori
Cohen, Jacob
Doebler, Robert
Hoang, Dzung
Hyde, Elizabeth
Lera, Matthew
Luzod, Louie T.
Mallinson, Mark
Marcu, Oana
Mohamedaly, Youssef
Ricco, Antonio J.
Rubins, Kathleen
Sgarlato, Gregory D.
Talavera, Rafael O.
Tong, Peter
Uribe, Eddie
Williams, Jeffrey
Wu, Diana
Yousuf, Rukhsana
Richey, Charles S.
Schonfeld, Julie
Almeida, Eduardo A. C.
Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station
title Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station
title_full Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station
title_fullStr Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station
title_full_unstemmed Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station
title_short Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station
title_sort microgravity validation of a novel system for rna isolation and multiplex quantitative real time pcr analysis of gene expression on the international space station
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587110/
https://www.ncbi.nlm.nih.gov/pubmed/28877184
http://dx.doi.org/10.1371/journal.pone.0183480
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