Molecular-scale interactions lie at the heart of cell biology, and super-resolution microscopy has emerged as a powerful tool for measurements inside cells. However, the current state-of-the-art does not include a generalizable method for mapping, measuring, and understanding real-time motions and biochemical interactions of pairs of mobile, dynamic components within cells. This gap is particularly critical in bacteria cells, in which many microscopy technologies are unproven or unfeasible due to small size and impenetrable walls. Something fundamentally different is needed: a new approach to understanding subcellular biochemistry in cells in real time. Thus, we aim to bridge single-molecule tracking, super-resolution imaging, and probabilistic statistical modeling to study pairs of molecules with the long-term goal of mapping the biochemistry of subcellular components in living bacteria cells. This exploratory proposal will develop interaction maps in living bacteria cells with two specific aims: (1) To observe pairs of mobile proteins and genetic loci with fluorescent protein fusions, CRISPR-dCas9 labeling, and super-resolution fluorescence microscopy in living bacteria; and (2) To measure the dynamics and interactions of these subcellular pairs with single-molecule tracking, Bayesian inference, and statistical modeling. The tools developed in this project will immediately benefit single-molecule imaging research by increasing the attainable information content. Furthermore, by focusing on applications in bacterial cell biology, the tools developed in this project will have a widespread, positive biomedical impact by making accessible long-term, significant questions in microbial biology.

Public Health Relevance

Molecular-scale interactions govern cell biology, and super-resolution microscopy has emerged as a powerful tool for attaining nanoscopic maps of the inside of the cell. This work will develop fluorescent labeling, single- molecule microscopy, and image analysis algorithms to measure the dynamical interactions between pairs of proteins and genes inside living bacteria cells. This project will produce new methods that can be applied broadly to investigate bacterial cell biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21GM128022-01
Application #
9506434
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Sammak, Paul J
Project Start
2018-05-10
Project End
2020-04-30
Budget Start
2018-05-10
Budget End
2019-04-30
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Arts and Sciences
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109