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Volume 271,
Number 15,
Issue of April 12, 1996 pp. 8925-8935
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Characterization
of a Major Peritrophic Membrane Protein, Peritrophin-44, from the
Larvae of Lucilia cuprina cDNA AND DEDUCED AMINO ACID SEQUENCES
(Received for publication, December 22, 1995)
Chris M.
Elvin,
Tony
Vuocolo ,
Roger D.
Pearson,
Iain J.
East,
George
A.
Riding,
Craig H.
Eisemann,
Ross
L.
Tellam
The peritrophic membrane is a semi-permeable chitinous matrix
lining the gut of most insects and is thought to have important roles
in the maintenance of insect gut structure, facilitation of digestion,
and protection from invasion by microrganisms and parasites. Proteins
are integral components of this matrix, although the structures and
functions of these proteins have not been characterized in any detail.
The peritrophic membrane from the larvae of the fly Lucilia
cuprina, the primary agent of cutaneous myiasis in sheep, was
shown to contain six major integral peritrophic membrane proteins. Two
of these proteins, a 44-kDa glycoprotein (peritrophin-44) and a 48-kDa
protein (peritrophin-48) together represent >70% of the total mass
of the integral peritrophic membrane proteins. Peritrophin-44 was
purified and its complete amino acid sequence was determined by cloning
and sequencing the DNA complementary to its mRNA. The deduced amino
acid sequence codes for a protein of 356 amino acids containing an
amino-terminal signal sequence followed by five similar but
nonidentical domains, each of approximately 70 amino acids and
characterized by a specific register of 6 cysteines. One of these
domains was also present in the noncatalytic regions of chitinases from Brugia malayi, Manduca sexta, and Chelonus.
Peritrophin-44 has a uniform distribution throughout the larval
peritrophic membrane. Reverse transcriptase-polymerase chain reaction
detected the expression of peritrophin-44 in all three larval instars
but only trace levels in adult L. cuprina. The protein binds
specifically to tri-N-acetyl chitotriose and reacetylated
chitosan in vitro. It is concluded that the multiple
cysteine-rich domains in peritrophin-44 are responsible for binding to
chitin, the major constituent of peritrophic membrane. Peritrophin-44
probably has roles in the maintenance of peritrophic membrane structure
and in the determination of the porosity of the peritrophic membrane.
This report represents the first characterization of an insect
peritrophic membrane protein.

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