T h e c h a r a c t e r i s t i c s p i n e s o n t h e s u r f a c e o f t h e s c h i s t o s o m e f l a t w o r m t e g u m e n t c o n s i s t o f h e x a g o n a l l y p a c k e d a c t i n f i l a m e n t s . E l e c t r o n m i c r o s c o p y o f i s o l a t e d s p i n e s s h o w s t h a t t h e i r s t r u c t u r e is v e r y s i m i l a r t o t h a t o f o t h e r b u n d l e s o f a c t i n c r o s s -l i n k e d w i t h an a d d i t i o n a l p r o t e i n .One of the most severe and widespread of human diseases is caused by the parasitic schistosome flatworm. The life cycle of this blood fluke involves asexual larval reproduction in an intermediate snail host, giving rise to the infectious free-swimming cercarial form. After penetrating the human tissue, the worms develop into adults that become situated in the gut or bladder veins; the female generally lodges--in permanent copulation-in the ventral groove of the male worm. The surface of the male is studded with prominent rigid intracellular spines that may be critical in attachment.Our attention was drawn to these structures by the report that they consist of a "crystalline protein" (sic) (l). The size of the male worm (1-1.5 cm long and 1-mm thick) and the size of the spines (-2.5-3 #m in length) make it feasible to examine these structures by negative staining in the electron microscope. Scraping the surface with a sharp blade readily produces spines--often, however, in low yield. When negatively stained with uranyl acetate, these structures are seen to be comprised ofactin filaments aligned in register axially and spaced laterally in a regular array. The axial period is 385 A, and is divided into three bands (Fig. I a, c). This image is, in fact, very similar to that given by other actin bundles in a variety of systems. [1,0] view, the axial repeat shows two weak stain-excluding stripes due to protein cross-bridges between actin filaments, and one bright node (where the bridge is obscured by a filament lying directly over it). In the [1,1] view, three equivalent stripes are seen in each axial repeat (see reference 3 for details). The projected lateral repeat in the spine ( a ) is ~100 ,g, corresponding to a spacing between filaments of 100(2/~/3) = 116 g,. Insert in a shows the optical diffraction pattern of the lower portion of the spine in a. The pattern shows off meridional reflections on the 1st, 6th, and 7th layer lines characteristic of the actin helix. An additional meridional reflection is present on the 3rd layer line due to the crossbridges. Note that additional actin layer lines (generally not seen) are present. They are due to the contribution of the cross-bridges. Other weak reflections midway between layer lines indicate a longer true repeat of the structure. The actin bundles in the spines could be preserved by freezing the worms in liquid nitrogen in a mixture of 50% glycerol, 50% actin buffer (5 mM NaPO4, pH 7.4, 50 mM NaCl, 0.5 mM ATP.Na2, 0.5 mM CaCI2, 3 mM NAN3). Specimens negatively stained with 1% uranyl ace...