The goal of this research is to determine how the disassembly, turnover, and resculpting of cellular actin filament arrays is regulated by the concerted actions of GMF, Coronin, Srv2/CAP, Twinfilin, Abp1, Cofilin, and AIP1. Each of these core components of the eukaryotic actin machinery is conserved from yeast to humans and has been genetically implicated in promoting actin turnover and remodeling. However, the specific roles and mechanisms of each protein and how they function in groups are only beginning to be understood. The proposed research will elucidate how these factors interact and work together in novel multi-component mechanisms to control actin filament debranching, coalescence, severing, capping, and depolymerization. This will define the molecular basis of diverse biological processes that rely on characteristic actin network geometries and turnover rates, including cell motility, endocytosis, and intracellular transport of vesicles, organelles, and pathogens. To achieve these goals, we will combine genetics, biochemical assays, in vitro multi-wavelength single molecule TIRF microscopy, and live cell imaging approaches. Mechanisms elucidated at the single molecule level in vitro will be tested in vivo using separation-of-function alleles for their importance in diverse biological processes. These include: yeast endocytosis and endosomal fusion with vacuoles, yeast actin cable turnover mediating intracellular transport, actin-based motility of Listeria in infected mammalian cells, and turnover of filopodia, stress fibers, and leading edge networks in mammalian cells.
The Aims are: (1) Test the hypothesis that actin filament networks are collaboratively debranched by mechanisms involving GMF, Coronin, Cofilin, and Srv2/CAP. (2) Test the hypothesis that Srv2/CAP and Abp1 interact to form a megadalton-sized complex that remodels actin networks by a novel mechanism of filament sliding and coalescence into bundles. (3) Test the hypothesis that novel mechanisms of actin filament end depolymerization mediated by Twinfilin and Srv2/CAP control the disassembly and length of cellular actin structures. (4) Test the hypothesis that differences in actin filament decoration and spatial organization govern how actin networks are remodeled and turned over.

Public Health Relevance

This grant investigates basic molecular and cellular mechanisms by which the actin cytoskeleton is remodeled and disassembled. The proposal focuses on seven proteins (GMF, Coronin, Cofilin, AIP1, Srv2/CAP, Abp1, and Twinfilin) that work in concert to induce rapid actin filament debranching, severing, capping and depolymerization. This work has direct relevance to human health, as GMF and Cofilin are important for learning, memory, and cognition, and alterations in their expression and solubility are linked to Alzheimer's disease; Srv2/CAP is linked to chronic obstructive pulmonary disease; Coronin is linked to immunodeficiencies and breast cancer; and Twinfilin is linked to the spread of lymphoma. For these reasons, this research has the potential to provide new insights into the underlying mechanisms of human disease. In addition, the work is designed to uncover basic mechanisms of cell biology that will contribute to our understanding of disease states in as-yet-unanticipated ways.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM063691-17
Application #
9672496
Study Section
Nuclear and Cytoplasmic Structure/Function and Dynamics Study Section (NCSD)
Program Officer
Ainsztein, Alexandra M
Project Start
2002-05-01
Project End
2021-04-30
Budget Start
2019-05-01
Budget End
2021-04-30
Support Year
17
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Brandeis University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
616845814
City
Waltham
State
MA
Country
United States
Zip Code
02453
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Goode, Bruce L; Sweeney, Meredith O; Eskin, Julian A (2018) GMF as an Actin Network Remodeling Factor. Trends Cell Biol 28:749-760
Hatano, Tomoyuki; Alioto, Salvatore; Roscioli, Emanuele et al. (2018) Rapid production of pure recombinant actin isoforms in Pichia pastoris. J Cell Sci 131:
Guo, Siyang; Sokolova, Olga S; Chung, Johnson et al. (2018) Abp1 promotes Arp2/3 complex-dependent actin nucleation and stabilizes branch junctions by antagonizing GMF. Nat Commun 9:2895
Howard, Nicole C; Marin, Nancy D; Ahmed, Mushtaq et al. (2018) Publisher Correction: Mycobacterium tuberculosis carrying a rifampicin drug resistance mutation reprograms macrophage metabolism through cell wall lipid changes. Nat Microbiol 3:1327
Johnston, Adam B; Hilton, Denise M; McConnell, Patrick et al. (2018) A novel mode of capping protein-regulation by twinfilin. Elife 7:
Wrasman, Kristie; Alioto, Salvatore L; Zhang, Yorke et al. (2018) A Flow Cytometry-Based Phenotypic Screen To Identify Novel Endocytic Factors in Saccharomyces cerevisiae. G3 (Bethesda) 8:1497-1512
Sokolova, Olga S; Chemeris, Angelina; Guo, Siyang et al. (2017) Structural Basis of Arp2/3 Complex Inhibition by GMF, Coronin, and Arpin. J Mol Biol 429:237-248
Mohapatra, Lishibanya; Goode, Bruce L; Jelenkovic, Predrag et al. (2016) Design Principles of Length Control of Cytoskeletal Structures. Annu Rev Biophys 45:85-116
Chin, Samantha M; Jansen, Silvia; Goode, Bruce L (2016) TIRF microscopy analysis of human Cof1, Cof2, and ADF effects on actin filament severing and turnover. J Mol Biol 428:1604-16

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