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  3. Isolation, N-glycosylations and Function of a Hyaluronidase-Like Enzyme from the Venom of the Spider Cupiennius salei.
 

Isolation, N-glycosylations and Function of a Hyaluronidase-Like Enzyme from the Venom of the Spider Cupiennius salei.

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BORIS DOI
10.7892/boris.74980
Date of Publication
2015
Publication Type
Article
Division/Institute

Departement für Chemi...

Institut für Ökologie...

Contributor
Biner, Olivier Felixorcid-logo
Departement für Chemie und Biochemie (DCB)
Trachsel, Christian
Departement für Chemie und Biochemie (DCB)
Moser, Aline
Institut für Ökologie und Evolution (IEE)
Kopp, Lukas
Departement für Chemie und Biochemie (DCB)
Langenegger, Nicolas
Institut für Ökologie und Evolution (IEE)
Kämpfer, Urs
Departement für Chemie und Biochemie (DCB)
von Ballmoos, Christophorcid-logo
Departement für Chemie und Biochemie (DCB)
Nentwig, Wolfgang
Institut für Ökologie und Evolution (IEE)
Schürch, Stefan
Departement für Chemie und Biochemie (DCB)
Schaller, Johann
Departement für Chemie und Biochemie (DCB)
Kuhn-Nentwig, Lucia Gerda
Institut für Ökologie und Evolution (IEE)
Subject(s)

500 - Science::540 - ...

500 - Science::570 - ...

500 - Science::590 - ...

Series
PLoS ONE
ISSN or ISBN (if monograph)
1932-6203
Publisher
Public Library of Science
Language
English
Publisher DOI
10.1371/journal.pone.0143963
PubMed ID
26630650
Description
STRUCTURE OF CUPIENNIUS SALEI VENOM HYALURONIDASE

Hyaluronidases are important venom components acting as spreading factor of toxic compounds. In several studies this spreading effect was tested on vertebrate tissue. However, data about the spreading activity on invertebrates, the main prey organisms of spiders, are lacking. Here, a hyaluronidase-like enzyme was isolated from the venom of the spider Cupiennius salei. The amino acid sequence of the enzyme was determined by cDNA analysis of the venom gland transcriptome and confirmed by protein analysis. Two complex N-linked glycans akin to honey bee hyaluronidase glycosylations, were identified by tandem mass spectrometry. A C-terminal EGF-like domain was identified in spider hyaluronidase using InterPro. The spider hyaluronidase-like enzyme showed maximal activity at acidic pH, between 40-60°C, and 0.2 M KCl. Divalent ions did not enhance HA degradation activity, indicating that they are not recruited for catalysis.

FUNCTION OF VENOM HYALURONIDASES

Besides hyaluronan, the enzyme degrades chondroitin sulfate A, whereas heparan sulfate and dermatan sulfate are not affected. The end products of hyaluronan degradation are tetramers, whereas chondroitin sulfate A is mainly degraded to hexamers. Identification of terminal N-acetylglucosamine or N-acetylgalactosamine at the reducing end of the oligomers identified the enzyme as an endo-β-N-acetyl-D-hexosaminidase hydrolase. The spreading effect of the hyaluronidase-like enzyme on invertebrate tissue was studied by coinjection of the enzyme with the Cupiennius salei main neurotoxin CsTx-1 into Drosophila flies. The enzyme significantly enhances the neurotoxic activity of CsTx-1. Comparative substrate degradation tests with hyaluronan, chondroitin sulfate A, dermatan sulfate, and heparan sulfate with venoms from 39 spider species from 21 families identified some spider families (Atypidae, Eresidae, Araneidae and Nephilidae) without activity of hyaluronidase-like enzymes. This is interpreted as a loss of this enzyme and fits quite well the current phylogenetic idea on a more isolated position of these families and can perhaps be explained by specialized prey catching techniques.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/137353
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journal.pone.0143963.pdftextAdobe PDF2.96 MBpublishedOpen
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