Title
Molecular cloning, expression and immunological properties of LiD1, a protein from the dermonecrotic family of Loxosceles intermedia spider venom
Date Issued
01 December 2002
Access level
metadata only access
Resource Type
journal article
Author(s)
Kalapothakis E.
Araujo S.C.
De Castro C.S.
Mendes T.M.
Gomez M.V.
Mangili O.C.
Gubert I.C.
Universidade Federal de Minas Gerais
Abstract
The present report describes the identification and molecular characterization of LiD1, a protein expressed in the venom gland of the brown spider Loxosceles intermedia. LiD1 belongs to a family of proteins with dermonecrotic activity and members of this family have been found in spiders from the genus Loxosceles. The necrotic lesions caused by this group of proteins may lead to serious socio-economic problems such as surgical tissue reconstitution and even patient death. LiD1 was cloned using a cDNA library constructed from the venom gland of L. intermedia and antibodies against proteins with dermonecrotic activity isolated from the crude venom of this spider. The amino acid sequence deduced from the cDNA revealed a mature protein of approximately 31kDa, with a pI of 7.37. The cDNA also revealed the existence of a signal peptide, a propeptide and also an untranslated 3′ region with 218 nucleotides. LiD1 was expressed as a protein fused with β-galactoside protein using the vector pBK-CMV, resulting in the recombinant protein recLiD1 with important immunological properties. recLiD1 was strongly recognised by anti-dermonecrotic antibodies and was also able to generate reactive antibodies against native dermonecrotic proteins isolated from the venom of L. intermedia. © 2002 Elsevier Science Ltd. All rights reserved.
Start page
1691
End page
1699
Volume
40
Issue
12
Language
English
OCDE Knowledge area
Toxicología
Subjects
Scopus EID
2-s2.0-0036891354
PubMed ID
Source
Toxicon
ISSN of the container
00410101
Sponsor(s)
Funding text
This research was supported by grants from PADCT, PRONEX, CAPES and CNPq. We thank Dr Michael Richardson for critical comments and editorial assistance. The technical assistance of Dário José de Sousa with the in vivo assays is gratefully acknowledged. E. Kalapothakis and C. Chávez-Olórtegui are recipients of CNPq fellowships.
Sources of information:
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