The Binder of Rho GTPase protein family (BORG), also known as Cdc42 Effector Proteins, consists of five members (BORG1-5). Each member of this family is defined by a Cdc42/Rac Interactive Binding motif (CRIB) and BORG Homology domains, BH1, BH2, and BH3. BORG proteins are known to be the first regulators of the septin cytoskeleton in non-dividing mammal cells. Recent studies in CancerAssociated Fibroblasts (CAFs) have shown that BORG2 works with the septin cytoskeleton to stabilize actin filaments in stress fibers. Although, it is established that the BH3 domain of BORG proteins interacts with septin complexes, the region responsible for actin interaction is not clearly established. Here, we have designed an N-terminal and C-terminal series of BORG2 truncations based on conserved regions in the sequence. By employing Tetramethylrhodamine (TMR) maleimide labeling at a unique cysteine, we have developed a fluorescence anisotropy assay for actin binding. Using this assay, we have established the region necessary and sufficient for actin binding. Notably, this region differs from a previously proposed actin binding site and exists in other BORG proteins, suggesting that the actin interaction may be a widespread and previously unrecognized feature of the BORG protein family.
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Details
Title
Identification of the BORG2/Cdc42EP3 Actin Binding Element
Creators
Prajakta Dilipkumar Mehetre
Contributors
Shae B. Padrick (Advisor)
Awarding Institution
Drexel University
Degree Awarded
Master of Science (M.S.)
Publisher
Drexel University; Philadelphia, Pennsylvania
Number of pages
vii, 77 pages
Resource Type
Thesis
Language
English
Academic Unit
Biochemistry and Molecular Biology; College of Medicine; Drexel University
Other Identifier
991014833149504721
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