Abstract

Eukaryotic cells are building blocks to complex living systems, characterized by membrane-bound organelles. Studying how eukaryotic organelles react to cellular growth and size increase is crucial, but it demands biochemical and biophysical manipulations, as well as quantitative observation tools in microscopy. We developed a multi-color yeast strain with tagged fluorescent proteins, enabling systematic measurements of 6 organelles inside each cell using spectral confocal microscopy. These measurements provided insights into how organelle biogenesis is coordinated with cellular size and growth rate regulation via different signaling pathways. To explore cellular growth under dynamic conditions, I utilized deep learning for organelle recognition using low-power bright field fluorescent microscopy. This technique maintains high spectral resolution while minimizing photodamage and enabling timelapse acquisition. Training output statistics demonstrated excellent fidelity to the target. The work in this thesis lays a foundation for capturing how organelle dynamics and cellular growth interrelate

Committee Chair

Shankar Mukherji

Degree

Doctor of Philosophy (PhD)

Author's Department

Physics

Author's School

Graduate School of Arts and Sciences

Document Type

Dissertation

Date of Award

8-14-2023

Language

English (en)

Author's ORCID

https://orcid.org/0000-0003-2902-7867

Included in

Physics Commons

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