Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783261939792609280 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5587110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT parramacarena microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT jungjimmy microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT boonetravisd microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT tranluan microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT blaberelizabetha microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT brownmark microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT chinmatthew microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT chinntori microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT cohenjacob microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT doeblerrobert microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT hoangdzung microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT hydeelizabeth microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT leramatthew microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT luzodlouiet microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT mallinsonmark microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT marcuoana microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT mohamedalyyoussef microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT riccoantonioj microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT rubinskathleen microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT sgarlatogregoryd microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT talaverarafaelo microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT tongpeter microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT uribeeddie microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT williamsjeffrey microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT wudiana microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT yousufrukhsana microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT richeycharless microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT schonfeldjulie microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation AT almeidaeduardoac microgravityvalidationofanovelsystemforrnaisolationandmultiplexquantitativerealtimepcranalysisofgeneexpressionontheinternationalspacestation |