Characterising the association of latency with alpha sub(1)-antitrypsin polymerisation using a novel monoclonal antibody

alpha sub(1)-Antitrypsin is primarily synthesised in the liver, circulates to the lung and protects pulmonary tissues from proteolytic damage. The Z mutant (Glu342Lys) undergoes inactivating conformational change and polymerises. Polymers are retained within the hepatocyte endoplasmic reticulum (ER) in homozygous (PiZZ) individuals, predisposing the individuals to hepatic cirrhosis and emphysema. Latency is an analogous process of inactivating, intra-molecular conformational change and may co-occur with polymerisation. However, the relationship between latency and polymerisation remained unexplored in the absence of a suitable probe. We have developed a novel monoclonal antibody specific for latent alpha sub(1)-antitrypsin and used it in combination with a polymer-specific antibody, to assess the association of both conformers in vitro, in disease and during augmentation therapy. In vitro kinetics analysis showed polymerisation dominated the pathway but latency could be promoted by stabilising monomeric alpha sub(1)-antitrypsin. Polymers were extensively produced in hepatocytes and a cell line expressing Z alpha sub(1)-antitrypsin but the latent protein was not detected despite manipulation of the secretory pathway. However, alpha sub(1)-antitrypsin augmentation therapy contains latent alpha sub(1)-antitrypsin, as did the plasma of 63/274 PiZZ individuals treated with augmentation therapy but 0/264 who were not receiving this medication (p < 10 super(-14)). We conclude that latent alpha sub(1)-antitrypsin is a by-product of the polymerisation pathway, that the intracellular folding environment is resistant to formation of the latent conformer but that augmentation therapy introduces latent alpha sub(1)-antitrypsin into the circulation. A suite of monoclonal antibodies and methodologies developed in this study can characterise alpha sub(1)-antitrypsin folding and conformational transitions, and screen methods to improve augmentation therapy.