The paper reports a 73-fold purification of rabbit serum paraoxonase/arylesterase with 31% recovery through four column steps (Cibacron Blue 3GA-agarose, Sephadex G-75, DEAE-Trisacryl M, second G-75), yielding two active bands at 35,000 and 38,000 Da. Upon electroelution and re-analysis, higher molecular weight inactive bands appeared at 43,000 and 48,000 Da, yet all four bands shared an identical amino-terminal sequence (AKLTALTLLGLGLALFDGQK), supporting unfolding rather than distinct protein species as the explanation .
A central contribution was refuting Mackness et al.'s claim that human serum contains separate paraoxonases and arylesterases. Using activity stains for both paraoxon and β-naphthylacetate after gel electrophoresis, the authors showed the same protein bands hydrolyze both substrates, consistent with Gan et al. (1991) and Smolen et al. (1991) . This resolution proved pivotal for the field, since later reviews confirm PON1's paraoxonase, arylesterase, and lactonase activities share a single active site .
Strengths: The renaturation-and-activity-staining strategy after SDS-PAGE was innovative and enabled direct confirmation that sequenced bands were catalytically active PON. Identical N-terminal sequences across four bands plus matching amino acid compositions (consistent with the concurrent rabbit cDNA from Hassett et al., 1991) provide strong identity evidence. Human PON purification achieved a non-blocked N-terminus, a practical advantage over Gan et al.'s preparation.
Limitations: (1) The molecular-weight shift upon re-electrophoresis was interpreted as unfolding or loss of associated material, but the mechanism was left unresolved — the authors explicitly state the reason is unknown. Glycosylation differences (5 potential N-sites in rabbit, 4 in human) were proposed but not tested. (2) Only single serum sources were characterized; the genetically determined human PON1 polymorphism was acknowledged but not addressed at the protein-purification level. (3) No yield is reported for the human purification beyond a 62-fold/18% endpoint, and the preparative gel approach is inherently low-yield. (4) The physiological substrate remained unknown — a point still flagged decades later . (5) Human PON activity-staining after SDS-PAGE was only occasionally successful, limiting cross-species generalization of the renaturation method.
This work directly enabled PON1 cloning (companion Hassett et al. paper) and oligonucleotide probe design. The observation that the hydrophobic N-terminus is a secreted-protein leader sequence retained after secretion — proposed as an HDL anchor — anticipated the now-established PON1–HDL association. However, the paper did not test whether the 35/38 kDa doublet reflects differential glycosylation versus proteolysis, did not sequence internal peptides, and relied on the assumption that identical N-termini imply identical proteins (now known insufficient given isoform complexity). Confidence in the core purification claims is high; confidence in the unfolding explanation is moderate and remains mechanistically unresolved.
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