The mechanism for pistol ribozyme was deduced through the identification of the products of the self-cleaving reaction. Through mass spectrometry, it was found that the products contain 5'-hydroxyl and 2',3'-cyclic phosphate functional groups. Reaction mechanism was concluded to involve 2'-OH nucleophilic attack by G53 on the phosphate bond connecting G53-U54. The process involves a trigonal bipyramidal penta-coordinated phosphorus center. N1 on G40 acts a general base in which it activates the nucleophile 2'-OH on G53. G32 acts as a general acid in which it neutralizes the developing negative charge on the intermediate.[2]
Under physiological pH and magnesium ion concentration, the rate constant of pistol ribozyme self-cleaving reaction was observed to be > 10 min−1. Under optimum condition (pH = 7.0 - 9.0, and magnesium concentration above 50 mM), the rate constant detected to be > 100 min−1. As magnesium concentration increases, the rate of reaction increases but starts to plateau around 50 mM.[2]
Self-cleaving reactions were observed in the presence of 0.1 mM of various monovalent and divalent metal ions such as magnesium, manganese, calcium, cobalt, nickel, cadmium, barium, sodium, and lithium. This implies that pistol ribozyme possess no specificity in the metal ion required in catalysis.[2]