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Full-Text Articles in Biology

An Essential Role For Endocytosis Of Rhodopsin Through Interaction Of Visual Arrestin With The Ap-2 Adaptor, Nicholas R. Orem, Luxi Xia, Patrick J. Dolph May 2006

An Essential Role For Endocytosis Of Rhodopsin Through Interaction Of Visual Arrestin With The Ap-2 Adaptor, Nicholas R. Orem, Luxi Xia, Patrick J. Dolph

Dartmouth Scholarship

Previously, we have identified a class of retinal degeneration mutants in Drosophila in which the normally transient interaction between arrestin2 (Arr2) and rhodopsin is stabilized and the complexes are rapidly internalized into the cell body by receptor-mediated endocytosis. The accumulation of protein complexes in the cytoplasm eventually results in photoreceptor cell death. We now show that the endocytic adapter protein AP-2 is essential for rhodopsin endocytosis through an Arr2-AP-2beta interaction, and mutations in Arr2 that disrupt its interaction with the beta subunit of AP-2 prevent endocytosis-induced retinal degeneration. We further demonstrate that if the interaction between Arr2 and AP-2 is …


A Kinesin-Like Calmodulin-Binding Protein In Chlamydomonas: Evidence For A Role In Cell Division And Flagellar Functions, Erin E. Dymek, Daniel Goduti, Tal Kramer, Elizabeth F. Smith May 2006

A Kinesin-Like Calmodulin-Binding Protein In Chlamydomonas: Evidence For A Role In Cell Division And Flagellar Functions, Erin E. Dymek, Daniel Goduti, Tal Kramer, Elizabeth F. Smith

Dartmouth Scholarship

Kinesin-like calmodulin-binding protein, KCBP, is a novel member of the C-kinesin superfamily first discovered in flowering plants. This minus-end-directed kinesin exhibits Ca(2+)-calmodulin-sensitive motor activity in vitro and has been implicated in trichome morphogenesis and cell division. A homologue of KCBP is also found in the unicellular, biflagellate green alga Chlamydomonas reinhardtii (CrKCBP). Unlike plant cells, Chlamydomonas cells do not form trichomes and do not assemble a phragmoplast before cell division. To test whether CrKCBP is involved in additional microtubule-based processes not observed in plants, we generated antibodies against the putative calmodulin-binding domain and used these antibodies in biochemical and localization …