FEBS Letters
Volume 582, Issue 16 , Pages 2382-2386, 9 July 2008

Human neprilysin-2 (NEP2) and NEP display distinct subcellular localisations and substrate preferences

Edited by Ned Mantei

Proteolysis Research Group, Institute of Molecular and Cellular Biology, University of Leeds, Leeds LS2 9JT, UK

Received 14 May 2008; received in revised form 28 May 2008; accepted 29 May 2008. published online 06 June 2008.

Abstract 

Neprilysin-2 (NEP2) is a novel metallopeptidase homologous to neprilysin (NEP), an enzyme involved in regulation of neuropeptide signalling. NEP2 exists as two alternatively spliced isoforms, NEP2 and NEP2Δ. In this study, we cloned and expressed both human isoforms. Human NEP2 exists as a membrane-bound and soluble enzyme, whereas human NEP2Δ exists as two membrane-bound glycoforms, localised to the ER and plasma membrane. Surprisingly, NEP2 substrate specificity and inhibitor binding was distinct from that of human NEP, suggesting that NEP and NEP2 play distinct physiological roles in humans, and human NEP2 differs markedly from its rodent homologues.

Keywords: Neprilysin, Neprilysin-2, M13 metallopeptidase, Thiorphan, Phosphoramidon

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PII: S0014-5793(08)00476-6

doi:10.1016/j.febslet.2008.05.046

FEBS Letters
Volume 582, Issue 16 , Pages 2382-2386, 9 July 2008