Over the past half-century, biologists have generated a critical mass of knowledge and many compelling hypotheses about how chromatin, a collection of proteins and RNA scaffolded to DNA, regulates gene expression. This knowledge has the potential to transform our understanding of development and disease and spur new therapeutic strategies. To realize this potential, new experimental tools are needed to directly test existing hypotheses and reveal the functions of chromatin components. Of particular use would be approaches that directly and specifically track the biochemical and biophysical states of chromatin in live cells. This would unlock our ability to study dynamic changes in chromatin state in response to cellular perturbations. Observing intracellular events in temporal sequence would also enable functional studies demonstrating changes in gene regulation in direct response to changes in chromatin state. Towards this goal, we will develop small proteins that bind specific biochemical chromatin modifications. These binders will be genetically encoded, enabling their use in live cell microscopy. The development of these chromatin binders will support a new frontier in chromatin research. They will build upon the information garnered from static maps of chromatin state and expand our understanding of chromatin into both the temporal and spatial dimensions.

Public Health Relevance

Chromatin, the collection of proteins and RNA bound across the genome, has been broadly implicated in disease and development. Yet our mechanistic understanding of how chromatin regulates these complex processes remains unclear due to a lack of tools to monitor chromatin dynamics in live cells. The development of sensors that can read out changes in chromatin state in live cells would drive unlock powerful new approaches to study chromatin regulation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21EB023377-02
Application #
9357582
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Rampulla, David
Project Start
2016-09-30
Project End
2019-07-31
Budget Start
2017-08-01
Budget End
2019-07-31
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
North Carolina State University Raleigh
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
042092122
City
Raleigh
State
NC
Country
United States
Zip Code
27695
Lee, Jessica B; Keung, Albert J (2018) Chromatin Immunoprecipitation in Human and Yeast Cells. Methods Mol Biol 1767:257-269
Sen, Dilara; Keung, Albert J (2018) Designing Epigenome Editors: Considerations of Biochemical and Locus Specificities. Methods Mol Biol 1767:65-87