As a first step in the biochemical and biomedical analyses of flagella
from Trichomonas vaginalis the flagella were isolated, purified, and
analyzed. The flagella were detached by mechanical shearing and a crud
e flagellar preparation was obtained by low-speed differential centrif
ugation. The crude flagellar preparation was subjected to further puri
fication by discontinuous sucrose density-gradient centrifugation. Ele
ctron micrographs (EM) of the purified flagella showed the typical 9 2 axonemal arrangement. The structural integrity and the flagellar me
mbrane were not destroyed by the deflagellation method or the purifica
tion scheme employed. The flagellar preparations were resolved by sodi
um dodecyl sulfate-polyacrylamide gel electrophoresis. The purified pr
eparation contained many flagellar enriched proteins ranging from 20 t
o 120 kDa. Three major proteins of 65 kDa and a doublet of about 50-58
kDa were observed. The protein patterns and EM appearance of the frac
tions were highly reproducible.