IDEAS home Printed from https://ideas.repec.org/a/plo/pbio00/3000786.html
   My bibliography  Save this article

SiCTeC: An inexpensive, easily assembled Peltier device for rapid temperature shifting during single-cell imaging

Author

Listed:
  • Benjamin D Knapp
  • Lillian Zhu
  • Kerwyn Casey Huang

Abstract

Single-cell imaging, combined with recent advances in image analysis and microfluidic technologies, have enabled fundamental discoveries of cellular responses to chemical perturbations that are often obscured by traditional liquid-culture experiments. Temperature is an environmental variable well known to impact growth and to elicit specific stress responses at extreme values; it is often used as a genetic tool to interrogate essential genes. However, the dynamic effects of temperature shifts have remained mostly unstudied at the single-cell level, due largely to engineering challenges related to sample stability, heatsink considerations, and temperature measurement and feedback. Additionally, the few commercially available temperature-control platforms are costly. Here, we report an inexpensive (

Suggested Citation

  • Benjamin D Knapp & Lillian Zhu & Kerwyn Casey Huang, 2020. "SiCTeC: An inexpensive, easily assembled Peltier device for rapid temperature shifting during single-cell imaging," PLOS Biology, Public Library of Science, vol. 18(11), pages 1-17, November.
  • Handle: RePEc:plo:pbio00:3000786
    DOI: 10.1371/journal.pbio.3000786
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3000786
    Download Restriction: no

    File URL: https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3000786&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pbio.3000786?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Enrique R. Rojas & Gabriel Billings & Pascal D. Odermatt & George K. Auer & Lillian Zhu & Amanda Miguel & Fred Chang & Douglas B. Weibel & Julie A. Theriot & Kerwyn Casey Huang, 2018. "The outer membrane is an essential load-bearing element in Gram-negative bacteria," Nature, Nature, vol. 559(7715), pages 617-621, July.
    2. André Maia Chagas, 2018. "Haves and have nots must find a better way: The case for open scientific hardware," PLOS Biology, Public Library of Science, vol. 16(9), pages 1-8, September.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Irina V. Mikheyeva & Jiawei Sun & Kerwyn Casey Huang & Thomas J. Silhavy, 2023. "Mechanism of outer membrane destabilization by global reduction of protein content," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    2. Augustinas Silale & Yiling Zhu & Jerzy Witwinowski & Robert E. Smith & Kahlan E. Newman & Satya P. Bhamidimarri & Arnaud Baslé & Syma Khalid & Christophe Beloin & Simonetta Gribaldo & Bert Berg, 2023. "Dual function of OmpM as outer membrane tether and nutrient uptake channel in diderm Firmicutes," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    3. Xiangfeng Lai & Mei-Ling Han & Yue Ding & Seong Hoong Chow & Anton P. Brun & Chun-Ming Wu & Phillip J. Bergen & Jhih-hang Jiang & Hsien-Yi Hsu & Benjamin W. Muir & Jacinta White & Jiangning Song & Jia, 2022. "A polytherapy based approach to combat antimicrobial resistance using cubosomes," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    4. Yuqian Qiao & Yingde Xu & Xiangmei Liu & Yufeng Zheng & Bo Li & Yong Han & Zhaoyang Li & Kelvin Wai Kwok Yeung & Yanqin Liang & Shengli Zhu & Zhenduo Cui & Shuilin Wu, 2022. "Microwave assisted antibacterial action of Garcinia nanoparticles on Gram-negative bacteria," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    5. Kerry R. Buchholz & Mike Reichelt & Matthew C. Johnson & Sarah J. Robinson & Peter A. Smith & Steven T. Rutherford & John G. Quinn, 2024. "Potent activity of polymyxin B is associated with long-lived super-stoichiometric accumulation mediated by weak-affinity binding to lipid A," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    6. Henri Voedts & Sean P. Kennedy & Guennadi Sezonov & Michel Arthur & Jean-Emmanuel Hugonnet, 2022. "Genome-wide identification of genes required for alternative peptidoglycan cross-linking in Escherichia coli revealed unexpected impacts of β-lactams," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    7. Zhenyu Ma & Sue C. Nang & Zhuo Liu & Jingyi Zhu & Kaijie Mu & Limei Xu & Min Xiao & Lushan Wang & Jian Li & Xukai Jiang, 2024. "Membrane lipid homeostasis dually regulates conformational transition of phosphoethanolamine transferase EptA," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    8. Han Gao & Yongmao Jiang & Lihua Wang & Guandong Wang & Wenqian Hu & Ling Dong & Sibao Wang, 2023. "Outer membrane vesicles from a mosquito commensal mediate targeted killing of Plasmodium parasites via the phosphatidylcholine scavenging pathway," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    9. Liselot Dewachter & Babette Deckers & Israel Mares-Mejía & Elen Louwagie & Silke Vercauteren & Paul Matthay & Simon Brückner & Anna-Maria Möller & Franz Narberhaus & Sibylle C. Vonesch & Wim Versées &, 2024. "The role of the essential GTPase ObgE in regulating lipopolysaccharide synthesis in Escherichia coli," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    10. Bob Schiffrin & Joel A. Crossley & Martin Walko & Jonathan M. Machin & G. Nasir Khan & Iain W. Manfield & Andrew J. Wilson & David J. Brockwell & Tomas Fessl & Antonio N. Calabrese & Sheena E. Radford, 2024. "Dual client binding sites in the ATP-independent chaperone SurA," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pbio00:3000786. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosbiology (email available below). General contact details of provider: https://journals.plos.org/plosbiology/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.