Several mycoplasma species are known to glide in the direction of the membrane protrusion (head-like structure), but the mechanism underlying this movement is entirely unknown. To identify proteins involved in the gliding mechanism, protein fractions of Mycoplasma mobile were analyzed for 10 gliding mutants isolated previously. One large protein (Gli349) was observed to be missing in a mutant m13 deficient in hemadsorption and glass binding. The predicted amino acid sequence indicated a 348,758-Da protein that was truncated at amino acid residue 1257 in the mutant. Immunofluorescence microscopy with a monoclonal antibody showed that Gli349 is localized at the head-like protrusion's base, which we designated the cell neck, and immunoelectron microscopy established that the Gli349 molecules are distributed all around this neck. The number of Gli349 molecules on a cell was estimated by immunoblot analysis to be 450 ؎ 200. The antibody inhibited both the hemadsorption and glass binding of M. mobile. When the antibody was used to treat gliding mycoplasmas, the gliding speed and the extent of glass binding were inhibited to similar extents depending on the concentration of the antibody. This suggested that the Gli349 molecule is involved not only in glass binding for gliding but also in movement. To explain the present results, a model for the mechanical cycle of gliding is discussed.Mycoplasmas are parasitic, small-genome bacteria that lack a peptidoglycan layer (28). Several mycoplasma species, including Mycoplasma pneumoniae, M. genitalium, M. pulmonis, M. gallisepticum, and M. mobile, have distinct cell polarity and exhibit gliding motility, a smooth translocation of cells across solid surfaces in the direction of the tapered end (17,22,36). The gliding motility of mycoplasmas is believed to be involved in pathogenicity, but the mechanisms underlying gliding motility have not been investigated well (19). Mycoplasmas have no surface structures, such as flagella or pili, or any homologs of genes that encode such structures. Neither do they have genes related to other bacterial motility systems or to eukaryotic motor proteins (5,11,13,21). These facts suggest that mycoplasmas glide by an entirely unknown mechanism.M. mobile, isolated in the early 1980s from the gills of a freshwater fish, is the fastest-gliding mycoplasma (18). M. mobile glides on glass in the direction of its tapered end, where its so-called head-like structure is. Its average speed is 2.0 to 4.5 m/s, about 3 to 7 times its cell length per second (32), and its maximum force can reach as high as 27 pN (23). It binds easily to glass and glides smoothly without pausing regardless of its growth stage. These distinct characteristics have allowed for detailed analyses of its gliding (9, 23-25, 32, 33) as well as for the isolation of gliding mutants, which are characterized by reduced or deficient gliding or by enhanced speed (26). However, no proteins related to gliding have been identified. In this study, we identified a huge protein that is truncated i...