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Volume 271,
Number 14,
Issue of April 5, 1996 pp. 8502-8508
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
The Peripheral
Complex of the Tobacco Hornworm V-ATPase Contains a Novel 13-kDa
Subunit G
(Received for publication, November 9, 1995; and in revised form, January 12,
1996)
Alexandra
Lepier
,
Ralph
Gräf
, ,
Masaaki
Azuma ,
Hans
Merzendorfer
,
William R.
Harvey
,
Helmut
Wieczorek
A prominent 16-kDa protein copurifies with the V-ATPase isolated
from both posterior midgut and Malpighian tubules of Manduca sexta larvae and thus was believed to represent a V-ATPase subunit.
[ C]N,N`-dicyclohexylcarbodiimide
labeling and its position on SDS-electrophoresis gels revealed that
this protein was different from the 17-kDa proteolipid. A cDNA clone
encoding a highly hydrophilic protein with a calculated molecular mass
of 13,692 Da was obtained by immunoscreening. Monospecific antibodies,
affinity-purified to the 13-kDa recombinant protein expressed in Escherichia coli, specifically recognized the 16-kDa protein
of the purified V-ATPase, confirming that a cDNA encoding this protein
had been cloned. In vitro translation of the cRNA showed that
the cloned 13-kDa subunit behaved like a 16-kDa protein on
SDS-electrophoresis gels. The cloned protein showed 37% amino acid
sequence identity to the 13-kDa V-ATPase subunit Vma10p recently cloned
from yeast and some similarity to subunit b of bacterial F-ATPases. In
contrast to the Vma10p protein, which behaved like a V subunit, the M. sexta 13-kDa protein behaved like a
V subunit, since it could be stripped from the membrane by
treatment with the chaotropic salt KI and by cold inactivation. When KI
dissociated V-ATPase subunits were reassociated by dialysis that
removed the KI, a soluble, 450-kDa complex of the M. sexta V-ATPase could be purified by gel chromatography. This V complex consisted of subunits A, B, E, and the 13-kDa subunit,
confirming that the cloned protein is a new V-ATPase subunit and a
member of the peripheral V complex of the V-ATPase. We
designate this new V component subunit G.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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