Chymotrypsin inhibitor from Erythrina uariegata seeds

Involvement of amino acid residues within the primary binding loop in potent inhibitory activity toward chymotrypsin

Shiroh Iwanaga, Nobuyuki Yamasaki, Makoto Kimura

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

The stoichiometry of the interaction between Erythrina variegata chymotrypsin inhibitor ECI and chymotrypsin was reinvestigated by analysis of their complex with ultracentrifugation and with amino acid analysis of the components separated. The amino acid analysis clearly showed that the stoichiometry of ECI and chymotrypsin was 1:1, though the apparent molecular mass of the complex was estimated to be 60 kDa. To examine the contribution of Leu64 (the P1 residue) to the inhibitory activity of ECI, a complete set of mutated inhibitors in which the amino acid at position 64 was replaced by 19 other amino acid residues was constructed by means of site-directed mutagenesis. Potent inhibitory activities (K(i), 1.3-4.6 x 10-8 M) exceeding that of the wild-type ECI (K(i), 9.8 x 10-8 M) were present in the mutant proteins L64F, L64M, L64W, and L64Y. The inhibitory activity of the mutant L64R was practically identical to that of the wild-type ECI. All other mutants exhibited slightly decreased inhibitory activities with K(i) values of 1.9-4.6 x 10-7 M. These results indicate that ECI-chymotrypsin interaction involves not only the P1 site residue but also other residue(s) of ECI. A series of individual alanine mutations was then constructed in residues Gln62 (P3), Phe63 (P2), Ser65 (P1'), Thr66 (P2'), and Phe67 (P3') in order to evaluate the contribution of each residue in the primary binding loop to the inhibitory activity. Replacement of Gln62, Phe63, and Phe67 with Ala residues decreased the inhibitory activity, the K(i) values being increased by approximately 3-4-fold; but replacement of Ser65 and Thr66 had relatively little effect. This suggests that the P2, P3, and P3' residues, together with the P1 residue, in the primary binding loop play an important role in the inhibitory activity toward chymotrypsin.

Original languageEnglish
Pages (from-to)663-669
Number of pages7
JournalJournal of Biochemistry
Volume124
Issue number3
DOIs
Publication statusPublished - Jan 1 1998

Fingerprint

Erythrina
Chymotrypsin
Seed
Seeds
Amino Acids
Stoichiometry
Mutagenesis
Ultracentrifugation
Molecular mass
Mutant Proteins
Site-Directed Mutagenesis
Alanine
Mutation

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology

Cite this

Chymotrypsin inhibitor from Erythrina uariegata seeds : Involvement of amino acid residues within the primary binding loop in potent inhibitory activity toward chymotrypsin. / Iwanaga, Shiroh; Yamasaki, Nobuyuki; Kimura, Makoto.

In: Journal of Biochemistry, Vol. 124, No. 3, 01.01.1998, p. 663-669.

Research output: Contribution to journalArticle

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abstract = "The stoichiometry of the interaction between Erythrina variegata chymotrypsin inhibitor ECI and chymotrypsin was reinvestigated by analysis of their complex with ultracentrifugation and with amino acid analysis of the components separated. The amino acid analysis clearly showed that the stoichiometry of ECI and chymotrypsin was 1:1, though the apparent molecular mass of the complex was estimated to be 60 kDa. To examine the contribution of Leu64 (the P1 residue) to the inhibitory activity of ECI, a complete set of mutated inhibitors in which the amino acid at position 64 was replaced by 19 other amino acid residues was constructed by means of site-directed mutagenesis. Potent inhibitory activities (K(i), 1.3-4.6 x 10-8 M) exceeding that of the wild-type ECI (K(i), 9.8 x 10-8 M) were present in the mutant proteins L64F, L64M, L64W, and L64Y. The inhibitory activity of the mutant L64R was practically identical to that of the wild-type ECI. All other mutants exhibited slightly decreased inhibitory activities with K(i) values of 1.9-4.6 x 10-7 M. These results indicate that ECI-chymotrypsin interaction involves not only the P1 site residue but also other residue(s) of ECI. A series of individual alanine mutations was then constructed in residues Gln62 (P3), Phe63 (P2), Ser65 (P1'), Thr66 (P2'), and Phe67 (P3') in order to evaluate the contribution of each residue in the primary binding loop to the inhibitory activity. Replacement of Gln62, Phe63, and Phe67 with Ala residues decreased the inhibitory activity, the K(i) values being increased by approximately 3-4-fold; but replacement of Ser65 and Thr66 had relatively little effect. This suggests that the P2, P3, and P3' residues, together with the P1 residue, in the primary binding loop play an important role in the inhibitory activity toward chymotrypsin.",
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