IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v13y2022i1d10.1038_s41467-022-34076-0.html
   My bibliography  Save this article

Engineered helicase replaces thermocycler in DNA amplification while retaining desired PCR characteristics

Author

Listed:
  • Momčilo Gavrilov

    (Johns Hopkins University School of Medicine)

  • Joshua Y. C. Yang

    (Johns Hopkins University School of Medicine)

  • Roger S. Zou

    (Johns Hopkins University School of Medicine)

  • Wen Ma

    (University of California)

  • Chun-Ying Lee

    (Johns Hopkins University)

  • Sonisilpa Mohapatra

    (Johns Hopkins University School of Medicine)

  • Jimin Kang

    (Johns Hopkins University)

  • Ting-Wei Liao

    (Johns Hopkins University)

  • Sua Myong

    (Johns Hopkins University)

  • Taekjip Ha

    (Johns Hopkins University School of Medicine
    Johns Hopkins University School of Medicine
    Johns Hopkins University
    Howard Hughes Medical Institute)

Abstract

Polymerase Chain Reaction (PCR) is an essential method in molecular diagnostics and life sciences. PCR requires thermal cycling for heating the DNA for strand separation and cooling it for replication. The process uses a specialized hardware and exposes biomolecules to temperatures above 95 °C. Here, we engineer a PcrA M6 helicase with enhanced speed and processivity to replace the heating step by enzymatic DNA unwinding while retaining desired PCR characteristics. We name this isothermal amplification method SHARP (SSB-Helicase Assisted Rapid PCR) because it uses the engineered helicase and single-stranded DNA binding protein (SSB) in addition to standard PCR reagents. SHARP can generate amplicons with lengths of up to 6000 base pairs. SHARP can produce functional DNA, a plasmid that imparts cells with antibiotic resistance, and can amplify specific fragments from genomic DNA of human cells. We further use SHARP to assess the outcome of CRISPR-Cas9 editing at endogenous genomic sites.

Suggested Citation

  • Momčilo Gavrilov & Joshua Y. C. Yang & Roger S. Zou & Wen Ma & Chun-Ying Lee & Sonisilpa Mohapatra & Jimin Kang & Ting-Wei Liao & Sua Myong & Taekjip Ha, 2022. "Engineered helicase replaces thermocycler in DNA amplification while retaining desired PCR characteristics," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34076-0
    DOI: 10.1038/s41467-022-34076-0
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-022-34076-0
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-022-34076-0?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. Ankur Jain & Ronald D. Vale, 2017. "RNA phase transitions in repeat expansion disorders," Nature, Nature, vol. 546(7657), pages 243-247, June.
    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. Siddharth Agarwal & Dino Osmanovic & Mahdi Dizani & Melissa A. Klocke & Elisa Franco, 2024. "Dynamic control of DNA condensation," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    2. Zhantao Shao & Jack Hu & Allison Jandura & Ronit Wilk & Matthew Jachimowicz & Lingfeng Ma & Chun Hu & Abby Sundquist & Indrani Das & Phillip Samuel-Larbi & Julie A. Brill & Henry M. Krause, 2024. "Spatially revealed roles for lncRNAs in Drosophila spermatogenesis, Y chromosome function and evolution," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    3. Jaimie Marie Stewart & Shiyi Li & Anli A. Tang & Melissa Ann Klocke & Martin Vincent Gobry & Giacomo Fabrini & Lorenzo Michele & Paul W. K. Rothemund & Elisa Franco, 2024. "Modular RNA motifs for orthogonal phase separated compartments," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    4. Brett M. O’Brien & Roumita Moulick & Gabriel Jiménez-Avalos & Nandakumar Rajasekaran & Christian M. Kaiser & Sarah A. Woodson, 2024. "Stick-slip unfolding favors self-association of expanded HTT mRNA," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    5. Sarah Rösing & Fabian Ullrich & Susann Meisterfeld & Franziska Schmidt & Laura Mlitzko & Marijana Croon & Ryan G Nattrass & Nadia Eberl & Julia Mahlberg & Martin Schlee & Anja Wieland & Philipp Simon , 2024. "Chronic endoplasmic reticulum stress in myotonic dystrophy type 2 promotes autoimmunity via mitochondrial DNA release," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    6. Damian Wollny & Benjamin Vernot & Jie Wang & Maria Hondele & Aram Safrastyan & Franziska Aron & Julia Micheel & Zhisong He & Anthony Hyman & Karsten Weis & J. Gray Camp & T.‐Y. Dora Tang & Barbara Tre, 2022. "Characterization of RNA content in individual phase-separated coacervate microdroplets," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    7. Clara Lopes Novo & Emily V. Wong & Colin Hockings & Chetan Poudel & Eleanor Sheekey & Meike Wiese & Hanneke Okkenhaug & Simon J. Boulton & Srinjan Basu & Simon Walker & Gabriele S. Kaminski Schierle &, 2022. "Satellite repeat transcripts modulate heterochromatin condensates and safeguard chromosome stability in mouse embryonic stem cells," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    8. Riccardo Calandrelli & Xingzhao Wen & John Lalith Charles Richard & Zhifei Luo & Tri C. Nguyen & Chien-Ju Chen & Zhijie Qi & Shuanghong Xue & Weizhong Chen & Zhangming Yan & Weixin Wu & Kathia Zaleta-, 2023. "Genome-wide analysis of the interplay between chromatin-associated RNA and 3D genome organization in human cells," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    9. Federica Raguseo & Yiran Wang & Jessica Li & Marija Petrić Howe & Rubika Balendra & Anouk Huyghebaert & Devkee M. Vadukul & Diana A. Tanase & Thomas E. Maher & Layla Malouf & Roger Rubio-Sánchez & Fra, 2023. "The ALS/FTD-related C9orf72 hexanucleotide repeat expansion forms RNA condensates through multimolecular G-quadruplexes," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    10. Zhefan Stephen Chen & Mingxi Ou & Stephanie Taylor & Ruxandra Dafinca & Shaohong Isaac Peng & Kevin Talbot & Ho Yin Edwin Chan, 2023. "Mutant GGGGCC RNA prevents YY1 from binding to Fuzzy promoter which stimulates Wnt/β-catenin pathway in C9ALS/FTD," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    11. Ofer Kimchi & Ella M. King & Michael P. Brenner, 2023. "Uncovering the mechanism for aggregation in repeat expanded RNA reveals a reentrant transition," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    12. Sudarsan Mugunthan & Lan Li Wong & Fernaldo Richtia Winnerdy & Stephen Summers & Muhammad Hafiz Ismail & Yong Hwee Foo & Tavleen Kaur Jaggi & Oliver W. Meldrum & Pei Yee Tiew & Sanjay H. Chotirmall & , 2023. "RNA is a key component of extracellular DNA networks in Pseudomonas aeruginosa biofilms," Nature Communications, Nature, vol. 14(1), pages 1-15, 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:13:y:2022:i:1:d:10.1038_s41467-022-34076-0. 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.