We will propose a method to detect changes in intramolecular structure or intermolecular organization based on orientation imaging of fluorescent single molecules. We will develop robust instrumentation for polarized fluorescence imaging exhibiting the speed and sensitivity required to monitor 3D angular changes of individual fluorophores that are rigidly connected to proteins of interest. While developing the optical arrangement and required acquisition and processing algorithms, we will use the system to monitor the organization of septin molecules in a filamentous fungus, Ashbya gossypii and in budding yeast. These model systems are used because they are highly amenable to imaging, molecular genetic and biochemical manipulations and the septins in these cells are well characterized. The septins are a highly conserved component of the cytoskeleton that are critical for cytokinesis and intracellular compartmentalization. Important insights have been gained about the steady state organization of septins using polarized fluorescence imaging approaches but never at the single molecule level.
As Aim 1 we will develop instrumentation and probe design for imaging the 3D orientation imaging of fluorescent single molecules.
For Aim 2 we will analyze the mechanisms of septin assembly and reorganization in vitro and in living cells.
For Aim 3, we will reveal the mechanisms of diffusion barrier function of septins in cellular membrane. In practice, we anticipate continuous back-and-forth transitions between those methods development and biological applications.

Public Health Relevance

Primary objective of the development of our fluorescent single molecule imaging is to reveal the mechanisms of molecular assembly and functions of septins in living cells. Septin functions are diverse and range from acting as scaffolds to concentrate signaling proteins to forming diffusion barriers that segregate membranes into discrete domains. Misregulation of septins has been implicated in a wide range of neuropathies including Alzheimer's, Parkinsons and Huntington's disease, autism as well as in various cancers. Understanding normal septin organization and assembly is essential to understand how their misfunction promotes disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM100160-02
Application #
8548372
Study Section
Enabling Bioanalytical and Imaging Technologies Study Section (EBIT)
Program Officer
Deatherage, James F
Project Start
2012-09-20
Project End
2017-08-31
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
2
Fiscal Year
2013
Total Cost
$300,441
Indirect Cost
$93,915
Name
Marine Biological Laboratory
Department
Type
DUNS #
001933779
City
Woods Hole
State
MA
Country
United States
Zip Code
02543
Bridges, Andrew A; Zhang, Huaiying; Mehta, Shalin B et al. (2014) Septin assemblies form by diffusion-driven annealing on membranes. Proc Natl Acad Sci U S A 111:2146-51