Analysis of glycolytic enzyme co-localization in Drosophila flight muscle
David T. Sullivan1,*,
R. MacIntyre2,
N. Fuda1,
J. Fiori1,
J. Barrilla1 and
L. Ramizel1
1 Department of Biology, Syracuse University, Syracuse, NY 13224,
USA
2 Department of Genetics and Molecular Biology, Cornell University, Ithaca,
NY 14853, USA

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Fig. 1. Glycerol-3-phosphate dehydrogenase (GPDH) localization in antibody-stained
myofibrils. Myofibrils were isolated from wild-type Drosophila
muscles and reacted with anti-GPDH serum and then reacted with fluorescein
isothiocyanate-labeled goat anti-rabbit serum and visualized as described in
Materials and methods.
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Fig. 2. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and aldolase localization
in antibody-stained myofibrils, as in Fig.
1.
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Fig. 3. Triose phosphate isomerase (TPI), phosphoglycerate kinase (PGK) and
phosphoglycerol mutase (PGLYM) localization in antibody-stained myofibrils, as
in Fig. 1.
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Fig. 4. A comparison between (A) phalloidin and (B) anti-glycerol-3-phosphate
dehydrogenase (GPDH) doubly stained myofibrils. Note that the thin Z-discs and
the broader M-lines in the phalloidin-stained myofibril coincide with fainter
anti-GPDH stained and brighter stained corresponding bands, respectively.
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Fig. 5. Myofibrils from wild-type Drosophila muscles incubated for 5 min
in contraction buffer and stained for glycerol-3-phosphate dehydrogenase
(GPDH). Note the reduced staining at the M-lines as compared with
Fig. 1.
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Fig. 6. Myofibrils from wild-type Drosophila muscles incubated in
contraction buffer for 20 min and simultaneously stained using
anti-glycerol-3-phosphate dehydrogenase (GPDH) and phalloidin. Note the
correspondence of the brightly fluorescent GPDH signal with the very faint,
narrow dark bands on the phalloidin-stained myofibril.
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Fig. 7. Glycerol-3-phosphate dehydrogenase (GPDH), glyceraldehyde-3-phosphate
dehydrogenase (GAPDH) and aldolase in antibody-stained myofibrils prepared
from GPDH null mutant flies. Visualized as in
Fig. 1. The exposure has been
extended so that an image of the weakly fluorescent myofibril would be
evident.
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Fig. 8. Triose phosphate isomerase (TPI), phosphoglycerate kinase (PGK) and
phosphoglycerol mutase (PGLYM) in antibody-stained myofibrils prepared from
glycerol-3-phosphate dehydrogenase (GPDH) null mutant flies. Visualized as in
Fig. 1. The exposure has been
extended so that an image of weakly fluorescent myofibril would be
evident.
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© The Company of Biologists Ltd 2003