ABSTRACT. Phagotrophic protists are major consumers of microbial biomass in aquatic ecosystems. However, biochemical mechanisms underlying prey recognition and phagocytosis by protists are not well understood. We investigated the potential roles of cell signaling mechanisms in chemosensory response to prey, and in capture of prey cells, by a marine ciliate (Uronema sp.) and a heterotrophic dinoflagellate (Oxyrrhis marina). Inhibition of protein kinase signal transduction biomolecules caused a decrease in both chemosensory response and predation. Inhibition of G-protein coupled receptor signaling pathways significantly decreased chemosensory response but had no effect on prey ingestion. Inhibitor compounds did not appear to affect general cell health, but had a targeted effect. These results support the idea that cell signaling pathways known in other eukaryotic organisms are involved in feeding behavior of free-living protists.Key Words. Cell signaling, chemosensory response, heterotrophic protist, Oxyrrhis marina, prey ingestion, Uronema sp.R ESPONSE of free-living phagotrophic protists to potential prey can be complex, resulting in selective ingestion or avoidance of prey cells (Boenigk and Arndt 2000a, b;Fenchel 1987;Strom 2000;Verity 1991;Wolfe 2000). Phagotrophic protists also exhibit chemosensory response to prey cells or to attractant/repellant compounds (Fenchel and Blackburn 1999;Fenchel and Jonsson 1988;Sibbald, Albright, and Sibbald 1987). However, little is known regarding specific biochemical mechanisms underlying protistan feeding behavior.At the cellular level, prey selection or chemosensory response is likely to be based on cell signaling events initiated by binding of specific ligand compounds to receptor molecules associated with cell membranes. Ligand-receptor binding at the cell surface can activate intracellular signal transduction, in which phosphorylation of specific proteins (e.g. G proteins or protein kinases) leads to processes in the cell that can result in changes in cell behavior, such as change in motility or phagocytosis of a prey cell. Phosphorylation of specific proteins is known to be a widely used molecular mechanism involved in switch-like outputs in cell behavior (Alberts et al. 2002;Gomperts, Kramer, and Tatham 2004;Hunter 2000;Rasmussen et al. 1996). Tyrosine kinase proteins in particular are important in phagocytosis in both animal and protist cells (King, Hittinger, and Caroll 2003;Renaud et al. 2004;Rosales 2005).G-protein coupled receptors (GPCRs) are a ubiquitous part of the cellular machinery in a range of eukaryotes, including protists (Van Haastert and Devreotes 2004). GPCRs have been show to be part of the chemosensory machinery used by immune cells in mammalian systems (Devreotes and Janetopoulos 2003;Haribabu et al. 1999) and in the slime mold Dictyostelium discoideum (Manahan et al. 2004;Traynor et al. 2000). Components of G-protein and tyrosine kinase signaling pathways appear highly conserved from sponges to vertebrates, and have been found in choanoflagellate...