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Carboxy-terminal truncation of oryzacystatin II by oryzacystatin-insensitive insect digestive proteinases.
Arch Biochem Biophys. 1995 Oct 01; 322(2):469-74.AB

Abstract

The biochemical interactions between digestive proteinases of the Coleoptera pest black vine weevil (Otiorynchus sulcatus) and two plant cysteine proteinase inhibitors, oryzacystatin I (OCI) and oryzacystatin II (OCII), were assessed using gelatin-polyacrylamide gel electrophoresis, OCI-affinity chromatography, and recombinant forms of the two plant inhibitors. The insect proteinases were resolved in gelatin-containing polyacrylamide gels as five major bands, only three of them being totally or partially inactivated by OCI and OCII. The maximal inhibitory effect of both OCs at pH 5.0 was estimated at 40% and the inhibition was stable with time despite the presence of OC-insensitive proteases, indicating the stability of the OCI and OCII effects. After removing OC-sensitive proteinases from the insect crude extract by OCI-affinity chromatography, the effects of the insect cystatin-insensitive proteases on the structural integrity of the free OCs were analyzed. While OCI remained stable, OCII was subjected to limited proteolysis leading to its gradual transformation into a approximately 10.5-kDa unstable intermediate, OCIIi. As shown by the degradation pattern of a glutathione S-transferase (GST)/OCII fusion protein, the appearance of OCIIi resulted from the C-terminal truncation of OCII. Either free or linked to GST, OCIIi was as active against papain and human cathepsin H as OCII, and the initial specificities of the inhibitor for these two cysteine proteinases were conserved after cleavage. Although these observations indicate the high conformational stability of OCII near its active (inhibitory) site, they also suggest a general conformational destabilization of this inhibitor following its initial cleavage, subsequently leading to its complete hydrolysis. This apparent susceptibility of OCII to proteolytic cleavage by the insect proteinases could have major implications when planning the use of this plant cystatin for insect pest control.

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Authors+Show Affiliations

Michaud D
Pacific Agriculture Research Centre, Agriculture and Agri-Food Canada, British Columbia.
Cantin L
No affiliation info available
Vrain TC
No affiliation info available

MeSH

AnimalsBinding SitesColeopteraCystatinsCysteine Proteinase InhibitorsDigestive SystemDose-Response Relationship, DrugElectrophoresis, Polyacrylamide GelEndopeptidasesGelatinHost-Parasite InteractionsPeptide FragmentsProtein ConformationRecombinant Fusion Proteins

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

7574723

Citation

Michaud, D, et al. "Carboxy-terminal Truncation of Oryzacystatin II By Oryzacystatin-insensitive Insect Digestive Proteinases." Archives of Biochemistry and Biophysics, vol. 322, no. 2, 1995, pp. 469-74.
Michaud D, Cantin L, Vrain TC. Carboxy-terminal truncation of oryzacystatin II by oryzacystatin-insensitive insect digestive proteinases. Arch Biochem Biophys. 1995;322(2):469-74.
Michaud, D., Cantin, L., & Vrain, T. C. (1995). Carboxy-terminal truncation of oryzacystatin II by oryzacystatin-insensitive insect digestive proteinases. Archives of Biochemistry and Biophysics, 322(2), 469-74.
Michaud D, Cantin L, Vrain TC. Carboxy-terminal Truncation of Oryzacystatin II By Oryzacystatin-insensitive Insect Digestive Proteinases. Arch Biochem Biophys. 1995 Oct 1;322(2):469-74. PubMed PMID: 7574723.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Carboxy-terminal truncation of oryzacystatin II by oryzacystatin-insensitive insect digestive proteinases. AU - Michaud,D, AU - Cantin,L, AU - Vrain,T C, PY - 1995/10/1/pubmed PY - 1995/10/1/medline PY - 1995/10/1/entrez SP - 469 EP - 74 JF - Archives of biochemistry and biophysics JO - Arch Biochem Biophys VL - 322 IS - 2 N2 - The biochemical interactions between digestive proteinases of the Coleoptera pest black vine weevil (Otiorynchus sulcatus) and two plant cysteine proteinase inhibitors, oryzacystatin I (OCI) and oryzacystatin II (OCII), were assessed using gelatin-polyacrylamide gel electrophoresis, OCI-affinity chromatography, and recombinant forms of the two plant inhibitors. The insect proteinases were resolved in gelatin-containing polyacrylamide gels as five major bands, only three of them being totally or partially inactivated by OCI and OCII. The maximal inhibitory effect of both OCs at pH 5.0 was estimated at 40% and the inhibition was stable with time despite the presence of OC-insensitive proteases, indicating the stability of the OCI and OCII effects. After removing OC-sensitive proteinases from the insect crude extract by OCI-affinity chromatography, the effects of the insect cystatin-insensitive proteases on the structural integrity of the free OCs were analyzed. While OCI remained stable, OCII was subjected to limited proteolysis leading to its gradual transformation into a approximately 10.5-kDa unstable intermediate, OCIIi. As shown by the degradation pattern of a glutathione S-transferase (GST)/OCII fusion protein, the appearance of OCIIi resulted from the C-terminal truncation of OCII. Either free or linked to GST, OCIIi was as active against papain and human cathepsin H as OCII, and the initial specificities of the inhibitor for these two cysteine proteinases were conserved after cleavage. Although these observations indicate the high conformational stability of OCII near its active (inhibitory) site, they also suggest a general conformational destabilization of this inhibitor following its initial cleavage, subsequently leading to its complete hydrolysis. This apparent susceptibility of OCII to proteolytic cleavage by the insect proteinases could have major implications when planning the use of this plant cystatin for insect pest control. SN - 0003-9861 UR - https://www.unboundmedicine.com/medline/citation/7574723/Carboxy_terminal_truncation_of_oryzacystatin_II_by_oryzacystatin_insensitive_insect_digestive_proteinases_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0003986185714907 DB - PRIME DP - Unbound Medicine ER -