12-Bromododecanoic acid binds inside the calyx of bovine beta-lactoglobulin

FEBS Lett. 1998 Nov 6;438(3):272-8. doi: 10.1016/s0014-5793(98)01199-5.

Abstract

The X-ray structure of bovine beta-lactoglobulin with the ligand 12-bromododecanoic acid as a model for fatty acids has been determined at a resolution of 2.23 A in the trigonal lattice Z form. The ligand binds inside the calyx, resolving a long-standing controversy as to where fatty-acid like ligands bind. The carboxylate head group lies at the surface of the molecule, and the lid to the calyx is open at the pH of crystallization (pH 7.3), consistent with the conformation observed in ligand-free bovine beta-lactoglobulin in lattice Z at pH 7.1 and pH 8.2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Cattle
  • Crystallography, X-Ray
  • Fatty Acids, Nonesterified / chemistry
  • Fatty Acids, Nonesterified / metabolism
  • Female
  • Hydrogen-Ion Concentration
  • Lactoglobulins / chemistry*
  • Lactoglobulins / metabolism
  • Lauric Acids / chemistry*
  • Ligands
  • Milk / chemistry
  • Models, Molecular
  • Protein Conformation*
  • Protein Structure, Secondary
  • Reproducibility of Results
  • Software

Substances

  • Fatty Acids, Nonesterified
  • Lactoglobulins
  • Lauric Acids
  • Ligands
  • 12-bromododecanoic acid