Purification of carboxyl ester lipase from human pancreas and the amino acid sequence of the N-terminal region

Biochem Biophys Res Commun. 1988 Sep 15;155(2):950-5. doi: 10.1016/s0006-291x(88)80588-6.

Abstract

A procedure for the purification of carboxyl ester lipase from human pancreas has been developed. The determined N-terminal 10 amino acid residues of the purified enzyme, NH2-Ala-Lys-Leu-Gly-Ala-Val-Tyr-Thr-Glu-Gly, was identical to the terminal of human milk bile salt-activated lipase. The human pancreatic carboxyl ester lipase has an apparent molecular weight slightly smaller than that of human milk bile salt-activated lipase (105,000 vs 125,000) as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Thus, it is possible that the human pancreatic carboxyl ester lipase and human milk bile salt-activated lipase could be produced by the same gene by a different splice or post-translational modification. Alternatively, they could simply be the products of two closely related but separate genes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Carboxylesterase
  • Carboxylic Ester Hydrolases / isolation & purification*
  • Humans
  • Milk, Human / enzymology
  • Molecular Sequence Data
  • Molecular Weight
  • Pancreas / enzymology*
  • Substrate Specificity

Substances

  • Carboxylic Ester Hydrolases
  • Carboxylesterase