The process of cell organization underlies fundamental biological processes ranging from polarized growth to multicellular development. The long-term goal of the Goodson laboratory is to understand the origins of this organization. Because many aspects of cell organization depend on the microtubule cytoskeleton, a major part of this initally diffuse problem can be reduced to two questions:: a) How is the microtubule cytoskeleton itself morphologically defined? b) How do other cellular components interact with microtubules? To answer these questions requires knowledge of the proteins that control microtubule (MT) dynamics and mediate cargo-MT interactions. This proposal focuses on CLIP-170, an evolutionarily conserved MT-binding protein that is involved in both processes. CLIP-170 also has the intriguing property of localizing dynamically to growing MT plus ends. The goal of this proposal is to define interactions between CLIP-170 and MTs how CLIP-170 associates with MTs, the mechanism and significance of its dynamic plus-end tracking behavior, and the precise effects it has on MT dynamics. This knowledge will establish CLIP-170 function and mechanism, aid in understanding other MT plus-end tracking proteins, and help define the regulation of MT growth.
Our Specific Aims are to: 1. Determine the affinity of CLIP-170 for different conformational states of tubulin/MTs by biophysical techniques including MT cosedimentation, fluorescence anisotropy, and surface plasmon resonance. This work will establish which interactions are physiologically relevant and test plus-end tracking mechanisms. 2. Define the effect of CLIP-170 on MT dynamics by performing in vitro MT dynamic instability assays in purified systems and in Xenopus extracts. This will define CLIP-170 activity and establish a system for further study of CLIP-170 regulation and protein partners. 3. Define the minimal plus-end tracking domain by transiently transfecting tagged CLIP-170 fragments into tissue culture cells and assaying their ability to track MT plus ends in vivo. This will allow us to establish the relationships between CLIP-170 structure, plus end tracking activity, and effects on MT dynamics, and will provide a simplified system for dissecting regulation involved in plus end tracking behavior.
| Gupta, Kamlesh K; Li, Chunlei; Duan, Aranda et al. (2013) Mechanism for the catastrophe-promoting activity of the microtubule destabilizer Op18/stathmin. Proc Natl Acad Sci U S A 110:20449-54 |
| Margolin, Gennady; Goodson, Holly V; Alber, Mark S (2011) Mean-field study of the role of lateral cracks in microtubule dynamics. Phys Rev E Stat Nonlin Soft Matter Phys 83:041905 |
| Skube, Susan B; Chaverri, José M; Goodson, Holly V (2010) Effect of GFP tags on the localization of EB1 and EB1 fragments in vivo. Cytoskeleton (Hoboken) 67:1-12 |
| Gupta, Kamlesh K; Joyce, Michelle V; Slabbekoorn, Aranda R et al. (2010) Probing interactions between CLIP-170, EB1, and microtubules. J Mol Biol 395:1049-62 |
| Zhu, Zhiqing C; Gupta, Kamlesh K; Slabbekoorn, Aranda R et al. (2009) Interactions between EB1 and microtubules: dramatic effect of affinity tags and evidence for cooperative behavior. J Biol Chem 284:32651-61 |
| Gupta, Kamlesh K; Paulson, Benjamin A; Folker, Eric S et al. (2009) Minimal plus-end tracking unit of the cytoplasmic linker protein CLIP-170. J Biol Chem 284:6735-42 |
| Gardner, Melissa K; Hunt, Alan J; Goodson, Holly V et al. (2008) Microtubule assembly dynamics: new insights at the nanoscale. Curr Opin Cell Biol 20:64-70 |
| Miller, Rita K; D'Silva, Sonia; Moore, Jeffrey K et al. (2006) The CLIP-170 orthologue Bik1p and positioning the mitotic spindle in yeast. Curr Top Dev Biol 76:49-87 |
| Margolin, Gennady; Gregoretti, Ivan V; Goodson, Holly V et al. (2006) Analysis of a mesoscopic stochastic model of microtubule dynamic instability. Phys Rev E Stat Nonlin Soft Matter Phys 74:041920 |
| Gregoretti, Ivan V; Margolin, Gennady; Alber, Mark S et al. (2006) Insights into cytoskeletal behavior from computational modeling of dynamic microtubules in a cell-like environment. J Cell Sci 119:4781-8 |
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