Salivary histatin 5 is a potent competitive inhibitor of the cysteine proteinase clostripain

被引:25
作者
Gusman, H
Grogan, J
Kagan, HM
Troxler, RF
Oppenheim, FG
机构
[1] Boston Univ, Goldman Sch Dent Med, Dept Periodontol & Oral Biol, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
关键词
histatin; 5; saliva; clostripain; cysteine proteinase inhibition; leupeptin; Clostridium histolyticum;
D O I
10.1016/S0014-5793(01)02077-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Histatin 5 is a low molecular weight salivary protein which is known to exhibit inhibitory activity against several proteinases, including the cysteine proteinases gingipains. The purpose of this study was to characterize the effect of salivary histatin on the proteolytic activity of the cysteine proteinase clostripain derived from the pathogen Clostridium histolyticum. Using a synthetic nitroanilide substrate, we studied in detail the inhibition of clostripain by histatin 5 and compared the effect of this peptide to that of leupeptin, a known competitive inhibitor of clostripain, It was found that the concentration of histatin 5 required to inhibit 50% of clostripain activity was 23.6 +/- 1.6 nM. Kinetic analysis revealed that histatin 5 is a competitive inhibitor of clostripain with an inhibition constant (K-i) of 10 nM. The K-i for the inhibition of clostripain activity against nitroanilide substrate by leupeptin was found to be 60 nM, significantly higher than that of histatin 5, Thus, histatin 5 inhibits clostripain more effectively than leupeptin and other cysteine protease inhibitors studied here. No significant proteolysis of histatin 5 was observed when histatin 5 was incubated at physiologic concentrations with clostripain, The potent inhibition of clostripain by histatin 5 points towards the possibility that this protein may prevent establishment of clostridial infections and therefore may have significant potential for the treatment of diseases associated with this enzyme. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 100
页数:4
相关论文
共 19 条
[1]  
Basak A, 1997, J PEPT RES, V49, P596
[2]  
GILLES AM, 1979, J BIOL CHEM, V254, P1462
[3]  
Hammes G, 1982, Enzyme catalysis and regulation
[4]   SEQUENCE-ANALYSIS AND CHARACTERIZATION OF THE PORPHYROMONAS-GINGIVALIS PRTC GENE, WHICH EXPRESSES A NOVEL COLLAGENASE ACTIVITY [J].
KATO, T ;
TAKAHASHI, N ;
KURAMITSU, HK .
JOURNAL OF BACTERIOLOGY, 1992, 174 (12) :3889-3895
[5]   CLOSTRIPAIN - CHARACTERIZATION OF THE ACTIVE-SITE [J].
KEMBHAVI, AA ;
BUTTLE, DJ ;
RAUBER, P ;
BARRETT, AJ .
FEBS LETTERS, 1991, 283 (02) :277-280
[6]  
LEPOW IH, 1952, J IMMUNOL, V69, P435
[7]   GROWTH-INHIBITORY AND BACTERICIDAL EFFECTS OF HUMAN-PAROTID SALIVARY HISTIDINE-RICH POLYPEPTIDES ON STREPTOCOCCUS-MUTANS [J].
MACKAY, BJ ;
DENEPITIYA, L ;
IACONO, VJ ;
KROST, SB ;
POLLOCK, JJ .
INFECTION AND IMMUNITY, 1984, 44 (03) :695-701
[8]  
MACLENNAN JD, 1958, J GEN MICROBIOL, V18, P1
[9]  
Mathews C K., 1996, Biochemistry
[10]  
Mitchell W M, 1977, Methods Enzymol, V47, P165