Substrate specificity of human kallikrein 2 (hK2) as determined by phage display technology

• Published in: European journal of biochemistry Vol. 269; no. 11; pp. 2747 - 2754
• Main Authors: Cloutier, Sylvain M., Chagas, Jair Ribeiro, Mach, Jean‐Pierre, Gygi, Christian M., Leisinger, Hans‐Jurg, Deperthes, David
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science, Ltd 01-06-2002
• Subjects: cyan fluorescent protein; Green Fluorescent Proteins; human kallikrein; Humans; Kinetics; Luminescent Proteins; Peptide Library; phage display; prostate cancer; substrate; Substrate Specificity - genetics; Tissue Kallikreins - genetics; Tissue Kallikreins - metabolism
• ISSN: 0014-2956; 1432-1033
• DOI: 10.1046/j.1432-1033.2002.02960.x

Human glandular kallikrein 2 (hK2) is a trypsin‐like serine protease expressed predominantly in the prostate epithelium. Recently, hK2 has proven to be a useful marker that can be used in combination with prostate specific antigen for screening and diagnosis of prostate cancer. The cleavage by hK2 of certain substrates in the proteolytic cascade suggest that the kallikrein may be involved in prostate cancer development; however, there has been very little other progress toward its biochemical characterization or elucidation of its true physiological role. In the present work, we adapt phage substrate technology to study the substrate specificity of hK2. A phage‐displayed random pentapeptide library with exhaustive diversity was generated and then screened with purified hK2. Phages displaying peptides susceptible to hK2 cleavage were amplified in eight rounds of selection and genes encoding substrates were transferred from the phage to a fluorescent system using cyan fluorescent protein (derived from green fluorescent protein) that enables rapid determination of specificity constants. This study shows that hK2 has a strict preference for Arg in the P1 position, which is further enhanced by a Ser in P′1 position. The scissile bonds identified by phage display substrate selection correspond to those of the natural biological substrates of hK2, which include protein C inhibitor, semenogelins, and fibronectin. Moreover, three new putative hK2 protein substrates, shown elsewhere to be involved in the biology of the cancer, have been identified thus reinforcing the importance of hK2 in prostate cancer development.