TY - JOUR
T1 - Ptychographic imaging of NaD1 induced yeast cell death
AU - Anthony, Nicholas
AU - Darmanin, Connie
AU - Bleackley, Mark R.
AU - Parisi, Kathy
AU - Cadenazzi, Guido
AU - Holmes, Susannah
AU - Anderson, Marilyn A.
AU - Nugent, Keith A.
AU - Abbey, Brian
N1 - Funding Information:
Australian Research Council (CE140100011, DP150104386).
Funding Information:
1Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Victoria 3086, Australia 2Nanophysics & NIC@IIT, Istituto Italiano Di Tecnologia, Via Enrico Melen 83, 16152 Genoa, Italy 3Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Victoria 3086, Australia 4Australian National University, ACT 0200, Australia
Publisher Copyright:
© 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
PY - 2019
Y1 - 2019
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85076634445&partnerID=8YFLogxK
U2 - 10.1364/BOE.10.004964
DO - 10.1364/BOE.10.004964
M3 - Article
AN - SCOPUS:85076634445
SN - 2156-7085
VL - 10
SP - 4964
EP - 4974
JO - Biomedical Optics Express
JF - Biomedical Optics Express
IS - 10
ER -