Enzymatic activity of toxic and non-toxic type 2 ribosome-inactivating proteins

Ribosome-inactivating proteins (RIPs) display adenine polynucleotide glycosylase activity on different nucleic acid substrates, which at the ribosomal level is responsible for the arrest of protein synthesis. Some type 2 RIPs, namely ricin and related proteins, are extremely toxic to mammalian cells...

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Veröffentlicht in:FEBS letters 2004-04, Vol.563 (1), p.219-222
Hauptverfasser: Barbieri, Luigi, Ciani, Marialibera, Girbés, Tomás, Liu, Wang-yi, Van Damme, Els J.M, Peumans, Willy J, Stirpe, Fiorenzo
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Sprache:eng
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Zusammenfassung:Ribosome-inactivating proteins (RIPs) display adenine polynucleotide glycosylase activity on different nucleic acid substrates, which at the ribosomal level is responsible for the arrest of protein synthesis. Some type 2 RIPs, namely ricin and related proteins, are extremely toxic to mammalian cells and animals whilst other type 2 RIPs (non-toxic type 2 RIPs) display three to four logs less toxicity. We studied whether a correlation exists between toxicity on cells and enzymatic activity on nucleic acids. All type 2 RIPs differ in their depurinating activity on the different substrates with differences of up to one to two logs. The toxicity of type 2 RIPs is independent of their enzymatic activity on nucleic acids or on ribosomes.
ISSN:0014-5793
1873-3468
DOI:10.1016/S0014-5793(04)00286-8