Perforin (P1) is a cytolytic protein with similarity to complement component C9. P1 has been described as a unique component of murine cytolytic T-cell and rat natural killer cell granules Previous studies indicated that human granules and P1 differed from murine granules and P1 in that they appeared to be cytolytically less active and lacked the haemolytic activity characteristic of P1. It has been suggested that P1, like C9, is under the control of the homologous restriction factor. Here we determine the primary structure of human P1, re-examine its functional properties, and address the question of homologous restriction.

The nucleotide sequence coding for the cytotoxic T-lymphocyte (CTL) protein perforin 1 (P1) has been determined and the corresponding protein sequence has been derived. Murine CTL cDNA libraries contained in the vector Agtll were screened by using a monospecific antiserum to purified P1. Three recombinant phages were isolated and their cDNA inserts were sequenced. The derived protein sequence contains 554 amino acids and displays, as expected, considerable homology with certain functional domains in the complement components C9, C8a, C8fi, and C7. The identity of P1 cDNA clones was verified by prokaryotic expression and the reactivities of antisera produced to the expressed proteins. In addition, antisera were produced to two synthetic peptides located in the center and C-terminal portions of P1. AU antisera reacted with purified P1. In Northern blot analyses, P1 cDNA probes recognized a 2.9-kilobase mRNA only in CTL. Perforin mRNA was found in all cloned CTL and in all mixed lymphocyte reactions that gave rise to cytotoxic cells. Perforin mRNA was also detected in virus-specific CTL that had been generated in vivo and isolated from liver tissue of mice infected with lymphocytic choriomeningitis virus. The cell-specific expression of perforin is consistent with its postulated role in cytolysis.

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A hemolytic activity associated with postnuclear supernatant fractions of Naegleriafowkri has been partially characterized in an attempt to isolate cytolytic molecules that may participate in naeglerial cytopathogenicity. Hemolysis by naeglerial postnuclear supernatant fractions was sensitive to heat and trypsin hydrolysis, and was inhibited by divalent cations. The m,%jority of the hemolytic activity was nonlatent and associated with a particle fraction sedimenting at 48,000 x g (maximum) for 1 h. This particle-associated hemolytic activity appears to be membrane associated, as high salt concentration, chelating agents, and pH extremes were ineffective in solubilizing the hemolytic activity, whereas treatment with 0.15% Zwittergent 3-12, a dipolar ionic detergent, results in 98% release of the sedimentable hemolysin. The sigmoidal nature of the progress curve of postnuclear supernatant hemolysis, as well as synergistic interactions between fractions of amoebal whole cell extracts, suggests that the hemolytic activity has a multicomponent nature, with at least two and possibly three components participating in the hemolytic event. The significance of these findings in the context of naeglerial cytopathogenicity is discussed.

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