Ricin uses arginine 235 as an anchor residue to bind to P-proteins of the ribosomal stalk.

ABSTRACT: Ricin toxin A chain (RTA) binds to stalk P-proteins to reach the α-sarcin/ricin loop (SRL) where it cleaves a conserved adenine. Arginine residues at the RTA/RTB interface are involved in this interaction. To investigate the individual contribution of each arginine, we generated single, double and triple arginine mutations in RTA. The R235A mutation reduced toxicity and depurination activity more than any other single arginine mutation in yeast. Further reduction in toxicity, depurination activity and ribosome binding was observed when R235A was combined with a mutation in a nearby arginine. RTA interacts with the ribosome via a two-step process, which involves slow and fast interactions. Single arginine mutations eliminated the fast interactions with the ribosome, indicating that they inc

SUBMITTER: Zhou Y 

PROVIDER: S-EPMC5322317 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature