La Trobe

Ptychographic imaging of NaD1 induced yeast cell death

journal contribution
posted on 2025-05-16, 02:01 authored by Nicholas Anthony, Connie DarmaninConnie Darmanin, Mark BleackleyMark Bleackley, Kathy ParisiKathy Parisi, Guido Cadenazzi, Susannah Holmes, Marilyn AndersonMarilyn Anderson, Keith NugentKeith Nugent, Brian AbbeyBrian Abbey
Characterising and understanding the mechanisms involved in cell death are especially important to combating threats to human health, particularly for the study of antimicrobial peptides and their effectiveness against pathogenic fungi. However, imaging these processes often relies on the use of synthetic molecules which bind to specific cellular targets to produce contrast. Here we study yeast cell death, induced by the anti-fungal peptide, NaD1. By treating yeast as a model organism we aim to understand anti-fungal cell death processes without relying on sample modification. Using a quantitative phase imaging technique, ptychography, we were able to produce label free images of yeast cells during death and use them to investigate the mode of action of NaD1. Using this technique we were able to identify a significant phase shift which provided a clear signature of yeast cell death. Additionally, ptychography identifies cell death much earlier than a comparative fluorescence study, providing new insights into the cellular changes that occur during cell death. The results indicate ptychography has great potential as a means of providing additional information about cellular processes which otherwise may be masked by indirect labelling approaches.

Funding

ARC Centre of Excellence in Advanced Molecular Imaging

Australian Research Council

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Molecular basis of synergy between PIs and defensins against fungi

Australian Research Council

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History

Publication Date

2019-10-01

Journal

Biomedical Optics Express

Volume

10

Issue

10

Pagination

11p. (p. 4964-4974)

Publisher

Optica Publishing Group

ISSN

2156-7085

Rights Statement

© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement