Abstract
Trichosanthin (TCS) is a type-I ribosome-inactivating protein (RIP) with wide spectrum of biological and pharmacological activities. In the present study, a potential site on the TCS molecule (position 120–123) is identified which may be important for the biological activities of TCS. By using site-directed mutagenesis, position 120–123 of TCS was either deleted or changed from LysIle-Arg-Glu (hydrophilic) to Ser-Ala-Gly-Gly (hydrophobic). Deletion of these residues rendered a TCS molecule completely deprived of ribosome inactivating activity, while hydrophobic replacement caused 4000-fold decrease in ribosome inactivating activity. The abortifacient activity of these two mutants was retained with decreased potency. This implies that position 120–123 of the native TCS molecule plays a critical role in maintaining its biological activity.
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