IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-36373-8.html
   My bibliography  Save this article

High-throughput single-molecule quantification of individual base stacking energies in nucleic acids

Author

Listed:
  • Jibin Abraham Punnoose

    (University at Albany, State University of New York)

  • Kevin J. Thomas

    (University at Albany, State University of New York)

  • Arun Richard Chandrasekaran

    (University at Albany, State University of New York)

  • Javier Vilcapoma

    (University at Albany, State University of New York)

  • Andrew Hayden

    (University at Albany, State University of New York)

  • Kacey Kilpatrick

    (University at Albany, State University of New York
    University at Albany, State University of New York)

  • Sweta Vangaveti

    (University at Albany, State University of New York)

  • Alan Chen

    (University at Albany, State University of New York
    University at Albany, State University of New York)

  • Thomas Banco

    (University at Albany, State University of New York)

  • Ken Halvorsen

    (University at Albany, State University of New York)

Abstract

Base stacking interactions between adjacent bases in DNA and RNA are important for many biological processes and in biotechnology applications. Previous work has estimated stacking energies between pairs of bases, but contributions of individual bases has remained unknown. Here, we use a Centrifuge Force Microscope for high-throughput single molecule experiments to measure stacking energies between adjacent bases. We found stacking energies strongest between purines (G|A at −2.3 ± 0.2 kcal/mol) and weakest between pyrimidines (C|T at −0.5 ± 0.1 kcal/mol). Hybrid stacking with phosphorylated, methylated, and RNA nucleotides had no measurable effect, but a fluorophore modification reduced stacking energy. We experimentally show that base stacking can influence stability of a DNA nanostructure, modulate kinetics of enzymatic ligation, and assess accuracy of force fields in molecular dynamics simulations. Our results provide insights into fundamental DNA interactions that are critical in biology and can inform design in biotechnology applications.

Suggested Citation

  • Jibin Abraham Punnoose & Kevin J. Thomas & Arun Richard Chandrasekaran & Javier Vilcapoma & Andrew Hayden & Kacey Kilpatrick & Sweta Vangaveti & Alan Chen & Thomas Banco & Ken Halvorsen, 2023. "High-throughput single-molecule quantification of individual base stacking energies in nucleic acids," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36373-8
    DOI: 10.1038/s41467-023-36373-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-36373-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-36373-8?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. Jessica L. Childs-Disney & Ewa Stepniak-Konieczna & Tuan Tran & Ilyas Yildirim & HaJeung Park & Catherine Z. Chen & Jason Hoskins & Noel Southall & Juan J. Marugan & Samarjit Patnaik & Wei Zheng & Chr, 2013. "Induction and reversal of myotonic dystrophy type 1 pre-mRNA splicing defects by small molecules," Nature Communications, Nature, vol. 4(1), pages 1-11, October.
    2. Emily M. Harcourt & Anna M. Kietrys & Eric T. Kool, 2017. "Chemical and structural effects of base modifications in messenger RNA," Nature, Nature, vol. 541(7637), pages 339-346, January.
    3. Darren Yang & Andrew Ward & Ken Halvorsen & Wesley P. Wong, 2016. "Multiplexed single-molecule force spectroscopy using a centrifuge," Nature Communications, Nature, vol. 7(1), pages 1-7, April.
    4. Brian J. Cafferty & David M. Fialho & Jaheda Khanam & Ramanarayanan Krishnamurthy & Nicholas V. Hud, 2016. "Spontaneous formation and base pairing of plausible prebiotic nucleotides in water," Nature Communications, Nature, vol. 7(1), 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. Zhangli Su & Ida Monshaugen & Briana Wilson & Fengbin Wang & Arne Klungland & Rune Ougland & Anindya Dutta, 2022. "TRMT6/61A-dependent base methylation of tRNA-derived fragments regulates gene-silencing activity and the unfolded protein response in bladder cancer," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    2. Àlex L González & Jordi Teixidó & José I Borrell & Roger Estrada-Tejedor, 2016. "On the Applicability of Elastic Network Models for the Study of RNA CUG Trinucleotide Repeat Overexpansion," PLOS ONE, Public Library of Science, vol. 11(3), pages 1-20, March.
    3. Ainara González-Iglesias & Aida Arcas & Ana Domingo-Muelas & Estefania Mancini & Joan Galcerán & Juan Valcárcel & Isabel Fariñas & M. Angela Nieto, 2024. "Intron detention tightly regulates the stemness/differentiation switch in the adult neurogenic niche," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    4. Ehsan Akbari & Melika Shahhosseini & Ariel Robbins & Michael G. Poirier & Jonathan W. Song & Carlos E. Castro, 2022. "Low cost and massively parallel force spectroscopy with fluid loading on a chip," Nature Communications, Nature, vol. 13(1), pages 1-11, 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:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36373-8. 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: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    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.