The Carbohydrate-Binding Site in Galectin-3 Is Preorganized To Recognize a Sugarlike Framework of Oxygens: Ultra-High-Resolution Structures and Water Dynamics
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- 作者：Kadhirvel Saraboji ; Maria H氓kansson ; Samuel Genheden ; Carl Diehl ; Johan Qvist ; Ulrich Weininger ; Ulf J. Nilsson ; Hakon Leffler ; Ulf Ryde ; Mikael Akke ; Derek T. Logan
- 刊名：Biochemistry
- 出版年：2012
- 出版时间：January 10, 2012
- 年：2012
- 卷：51
- 期：1
- 页码：296-306
- 全文大小：432K
- 年卷期：v.51,no.1(January 10, 2012)
- ISSN：1520-4995
文摘
The recognition of carbohydrates by proteins is a fundamental aspect of communication within and between living cells. Understanding the molecular basis of carbohydrate鈥損rotein interactions is a prerequisite for the rational design of synthetic ligands. Here we report the high- to ultra-high-resolution crystal structures of the carbohydrate recognition domain of galectin-3 (Gal3C) in the ligand-free state (1.08 脜 at 100 K, 1.25 脜 at 298 K) and in complex with lactose (0.86 脜) or glycerol (0.9 脜). These structures reveal striking similarities in the positions of water and carbohydrate oxygen atoms in all three states, indicating that the binding site of Gal3C is preorganized to coordinate oxygen atoms in an arrangement that is nearly optimal for the recognition of 尾-galactosides. Deuterium nuclear magnetic resonance (NMR) relaxation dispersion experiments and molecular dynamics simulations demonstrate that all water molecules in the lactose-binding site exchange with bulk water on a time scale of nanoseconds or shorter. Nevertheless, molecular dynamics simulations identify transient water binding at sites that agree well with those observed by crystallography, indicating that the energy landscape of the binding site is maintained in solution. All heavy atoms of glycerol are positioned like the corresponding atoms of lactose in the Gal3C complexes. However, binding of glycerol to Gal3C is insignificant in solution at room temperature, as monitored by NMR spectroscopy or isothermal titration calorimetry under conditions where lactose binding is readily detected. These observations make a case for protein cryo-crystallography as a valuable screening method in fragment-based drug discovery and further suggest that identification of water sites might inform inhibitor design.