IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0341464.html

PS Poly: A chain tracing algorithm to determine persistence length and categorize complex polymers by shape

Author

Listed:
  • Elizabeth A Conley
  • Creighton M Lisowski
  • Katherine G Schaefer
  • Harrison C Davison
  • Julie E Baguio
  • Ioan Kosztin
  • Gavin M King

Abstract

The fundamental molecules of life are polymers. Prominent examples include nucleic acids and proteins, both of which exhibit a large array of mechanical properties and three-dimensional shapes. The bending rigidity of individual polymers is quantified by the persistence length. The shape of a polymer, dictated by the topology of the polymer backbone, a line trace through the center of the polymer along the contour path, is also an important characteristic. Common biomolecular architectures include linear, cyclic (ring-like), and branched structures; combinations of these can also exist, as in complex polymer networks. Determination of persistence length and shape are largely informative to polymer function and stability in biological environments. Here we demonstrate Persistence length Shape Polymer (PS Poly), a near-fully automated algorithm designed to obtain key physical attributes from single molecule images obtained in physiologically relevant fluid conditions via atomic force microscopy. The algorithm, which involves image reduction via skeletonization followed by end point and branch point detection, is capable of rapidly analyzing thousands of polymers with subpixel precision. Algorithm outputs were verified by analysis of deoxyribonucleic acid, a very well characterized macromolecule. The method was further demonstrated by application to candidalysin, a recently discovered and complex virulence factor from Candida albicans. Candidalysin forms polymers of highly variable shape and contour length and represents the first peptide toxin identified in a human fungal pathogen. PS Poly is a robust and general algorithm. It can be used to extract fundamental information about polymer backbone stiffness, architecture, and more generally, polymerization mechanisms.

Suggested Citation

  • Elizabeth A Conley & Creighton M Lisowski & Katherine G Schaefer & Harrison C Davison & Julie E Baguio & Ioan Kosztin & Gavin M King, 2026. "PS Poly: A chain tracing algorithm to determine persistence length and categorize complex polymers by shape," PLOS ONE, Public Library of Science, vol. 21(2), pages 1-17, February.
  • Handle: RePEc:plo:pone00:0341464
    DOI: 10.1371/journal.pone.0341464
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0341464
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0341464&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0341464?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. David L. Moyes & Duncan Wilson & Jonathan P. Richardson & Selene Mogavero & Shirley X. Tang & Julia Wernecke & Sarah Höfs & Remi L. Gratacap & Jon Robbins & Manohursingh Runglall & Celia Murciano & Ma, 2016. "Candidalysin is a fungal peptide toxin critical for mucosal infection," Nature, Nature, vol. 532(7597), pages 64-68, April.
    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. Tingting Zhou & Norma V. Solis & Michaela Marshall & Qing Yao & Eric Pearlman & Scott G. Filler & Haoping Liu, 2025. "Fungal Als proteins hijack host death effector domains to promote inflammasome signaling," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
    2. Yu Liu & Ruina Wang & Jiacun Liu & Mengting Fan & Zi Ye & Yumeng Hao & Fei Xie & Ting Wang & Yuanying Jiang & Ningning Liu & Xiaoyan Cui & Quanzhen Lv & Lan Yan, 2024. "The vacuolar fusion regulated by HOPS complex promotes hyphal initiation and penetration in Candida albicans," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
    3. Dandan Yang & Mao Zhang & Chang Su & Bin Dong & Yang Lu, 2023. "Candida albicans exploits N-acetylglucosamine as a gut signal to establish the balance between commensalism and pathogenesis," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    4. Tingting Zhou & Norma V. Solis & Michaela Marshall & Qing Yao & Rachel Garleb & Mengli Yang & Eric Pearlman & Scott G. Filler & Haoping Liu, 2024. "Hyphal Als proteins act as CR3 ligands to promote immune responses against Candida albicans," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    5. Melissa R. Cruz & Shane Cristy & Shantanu Guha & Giuseppe Buda Cesare & Elena Evdokimova & Hiram Sanchez & Dominika Borek & Pedro Miramón & Junko Yano & Paul L. Fidel & Alexei Savchenko & David R. And, 2022. "Structural and functional analysis of EntV reveals a 12 amino acid fragment protective against fungal infections," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    6. Sophia U. J. Hitzler & Candela Fernández-Fernández & Kerstin Günther & Axel Dietschmann & Hrant Hovhannisyan & Anna Möslinger & Sophie Austermeier & Beatriz Cristóvão & Gianluca Vascelli & Teresa Zela, 2025. "Host albumin redirects Candida albicans metabolism to engage an alternative pathogenicity pathway," Nature Communications, Nature, vol. 16(1), pages 1-20, December.
    7. Ilan Zaffran & Pratibha Gaur & Prince Ofori & Yoav Charpak-Amikam & Hadas Pahima & David Shasha & Nir Osherov & Bernhard Hube & Ronen Ben-Ami & Julian R. Naglik & Ofer Mandelboim & Joana Vitte & Franc, 2025. "Eosinophil CD48 interactions with Candida albicans Als6 is protective in vitro and in mouse systemic candidiasis," Nature Communications, Nature, vol. 16(1), pages 1-14, December.
    8. Xionghui Ding & Hiroto Kambara & Rongxia Guo & Apurva Kanneganti & Maikel Acosta-Zaldívar & Jiajia Li & Fei Liu & Ting Bei & Wanjun Qi & Xuemei Xie & Wenli Han & Ningning Liu & Cunling Zhang & Xiaoyu , 2021. "Inflammasome-mediated GSDMD activation facilitates escape of Candida albicans from macrophages," Nature Communications, Nature, vol. 12(1), pages 1-24, December.
    9. Joy Lachat & Alice Pascault & Delphine Thibaut & Rémi Borgne & Jean-Marc Verbavatz & Allon Weiner, 2022. "Trans-cellular tunnels induced by the fungal pathogen Candida albicans facilitate invasion through successive epithelial cells without host damage," Nature Communications, Nature, vol. 13(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:plo:pone00:0341464. 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: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    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.