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Article
Effect of pH and ionic strength on μ- and m-calpain inhibition by calpastatin
Journal of Animal Science
  • K. R. Maddock, Iowa State University
  • Elisabeth J. Huff-Lonergan, Iowa State University
  • L. J. Rowe, Iowa State University
  • Steven M. Lonergan, Iowa State University
Document Type
Article
Publication Date
6-1-2005
Abstract

The objectives of this study were to determine the extent to which pH and ionic strength influence μ- and m-calpain activity and the inhibition of calpains by calpastatin. Calpastatin, μ-calpain, and m-calpain were purified from at-death porcine semimembranosus. μ-Calpain or m-calpain (0.45 U) were incubated with the calpain substrate Suc-Leu-Leu-Val-Tyr-7-amino-4-methyl coumarin in the presence of calpastatin (0, 0.15, or 0.30 U of calpain inhibitory activity) under the following pH and ionic strength conditions: pH 7.5 and 165 mM NaCl or 295 mM NaCl; pH 6.5 and 165 mM NaCl or 295 mM NaCl; and pH 6.0 and 165 mM NaCl or 295 mM NaCl. The reactions were initiated with addition of 100 μM (μ-calpain) or 1 mM CaCl2 (m-calpain), and calpain activity was recorded at 30 and 60 min. μ-Calpain had the greatest (P < 0.01) activity at pH 6.5 at each ionic strength. Higher ionic strength decreased μ-calpain activity (P< 0.01) at all pH conditions. Inhibition percent of μ-calpain by calpastatin was not affected by pH; however, it was influenced by ionic strength. Inhibition of μ-calpain by calpastatin was higher (P < 0.01) at 295 mM NaCl than at 165 mM NaCl when 0.3 units of calpastatin were included in the assay. Activity of m-calpain was greater (P < 0.01) at pH 7.5 than at pH 6.5. m-Calpain activity was not detected at pH 6.0. Inhibition of m-calpain was greater (P < 0.01) when 0.15 and 0.3 U calpastatin were added at pH 6.5 than 7.5 at 165 mM NaCl, whereas percentage inhibition of m-calpain was greater (P < 0.01) at 295 mM than 165 mM NaCl at pH 7.5 and 6.5. These observations provide new evidence that defines further the influence of pH decline and increased ionic strength on μ-calpain, m-calpain, and calpastatin activity, thereby helping to more accurately define a role for these enzymes in the process of postmortem tenderization.

Comments

This article is from Journal of Animal Science 83 (2005): 1370–1376. Posted with permission.

Copyright Owner
American Society of Animal Science
Language
en
Date Available
2014-02-24
File Format
application/pdf
Citation Information
K. R. Maddock, Elisabeth J. Huff-Lonergan, L. J. Rowe and Steven M. Lonergan. "Effect of pH and ionic strength on μ- and m-calpain inhibition by calpastatin" Journal of Animal Science Vol. 83 Iss. 6 (2005) p. 1370 - 1376
Available at: http://works.bepress.com/steven_lonergan/97/