Barbieri Luigi, Ciani Marialibera, Girbés Tomás, Liu Wang-Yi, Van Damme Els J M, Peumans Willy J, Stirpe Fiorenzo
Dipartimento di Patologia Sperimentale, Università di Bologna, I-40126 Bologna, Italy.
FEBS Lett. 2004 Apr 9;563(1-3):219-22. doi: 10.1016/S0014-5793(04)00286-8.
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.
核糖体失活蛋白(RIPs)在不同的核酸底物上表现出腺嘌呤多核苷酸糖基化酶活性,在核糖体水平上,这种活性会导致蛋白质合成的停滞。一些2型RIPs,即蓖麻毒素和相关蛋白,对哺乳动物细胞和动物具有极高的毒性,而其他2型RIPs(无毒2型RIPs)的毒性则低三到四个数量级。我们研究了细胞毒性与核酸酶活性之间是否存在相关性。所有2型RIPs在不同底物上的脱嘌呤活性不同,差异高达一到两个数量级。2型RIPs的毒性与其对核酸或核糖体的酶活性无关。