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7EKA

crystal structure of epigallocatechin binding with alpha-lactalbumin

Summary for 7EKA
Entry DOI10.2210/pdb7eka/pdb
DescriptorAlpha-lactalbumin, 2-(3,4,5-TRIHYDROXY-PHENYL)-CHROMAN-3,5,7-TRIOL (3 entities in total)
Functional Keywordsalpha-lactalbumin, epigallocatechin; epigallocatechin, ligase
Biological sourceBos taurus (cattle)
Total number of polymer chains1
Total formula weight14265.98
Authors
Ma, J.,Yao, Q.,Chen, X.,Zang, J. (deposition date: 2021-04-05, release date: 2023-11-08, Last modification date: 2024-11-13)
Primary citationMa, J.,Yao, Q.,Chen, X.,Lv, C.,Zang, J.,Zhao, G.
Weak Binding of Epigallocatechin to alpha-Lactalbumin Greatly Improves Its Stability and Uptake by Caco-2 Cells.
J.Agric.Food Chem., 69:8482-8491, 2021
Cited by
PubMed Abstract: Improving the stability and bioavailability of catechins is of great importance. Epigallocatechin (EGC), the major catechin in green tea, is a potent antioxidant with numerous attributed health benefits. However, the low permeability and stability limit its enrichment in the diet for preventive medicine. In this study, we explored the interaction of EGC and α-lactalbumin by spectroscopic, thermodynamic, and crystallographic methods. The isothermal titration calorimetry experiments elucidated that α-lactalbumin binds to EGC at a ratio of 1:1 with a low affinity of (4.01 ± 0.11) × 10 M. A crystal structure solved at a high resolution (1.2 Å) provided direct evidence for the weak interaction between EGC and α-lactalbumin at an atomic level. The novel binding site was discovered at the exterior surface of α-lactalbumin for the first time, supporting a new binding behavior. Consequently, our results demonstrated that the binding of α-lactalbumin to EGC could protect EGC against light-induced, thermal-induced, and pH-induced damage. More importantly, the formed complex has better bioaccessibility than unbound EGC, which was approved by a cell absorption experiment. Such research is beneficial for designing protein-based nanocarriers for polyphenols.
PubMed: 34286590
DOI: 10.1021/acs.jafc.1c03427
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.2 Å)
Structure validation

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