Launching Spiking Ligands into a Protein鈥揚rotein Interface: A Promising Strategy To Destabilize and Break Interface Formation in a tRNA Modifying Enzyme
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- 作者：Florian Immekus ; Luzi Jakob Barandun ; Michael Betz ; Fran莽ois Debaene ; St茅phanie Petiot ; Sarah Sanglier-Cianferani ; Klaus Reuter ; Fran莽ois Diederich ; Gerhard Klebe
- 刊名：ACS Chemical Biology
- 出版年：2013
- 出版时间：June 21, 2013
- 年：2013
- 卷：8
- 期：6
- 页码：1163-1178
- 全文大小：706K
- 年卷期：v.8,no.6(June 21, 2013)
- ISSN：1554-8937
文摘
Apart from competitive active-site inhibition of protein function, perturbance of protein鈥損rotein interactions by small molecules in oligodomain enzymes opens new perspectives for innovative therapeutics. tRNA鈥揼uanine transglycosylase (TGT), a potential target to treat shigellosis, is active only as the homodimer. Consequently, disruption of the dimer interface by small molecules provides a novel inhibition mode. A special feature of this enzyme is the short distance between active site and rim of the dimer interface. This suggests design of expanded active-site inhibitors decorated with rigid, needle-type substituents to spike into potential hot spots of the interaction interface. Ligands with attached ethinyl-type substituents have been synthesized and characterized by Kd measurements, crystallography, noncovalent mass spectrometry, and computer simulations. In contrast to previously determined crystal structures with nonextended active-site inhibitors, a well-defined loop-helix motif, involved in several contacts across the dimer interface, falls apart and suggests enhanced flexibility once the spiking ligands are bound. Mass spectrometry indicates significant destabilization but not full disruption of the complexed TGT homodimer in solution. As directed interactions of the loop-helix motif obviously do not determine dimer stability, a structurally conserved hydrophobic patch composed of several aromatic amino acids is suggested as interaction hot spot. The residues of this patch reside on a structurally highly conserved helix-turn-helix motif, which remains unaffected by the bound spiking ligands. Nevertheless, it is shielded from solvent access by the loop-helix motif that becomes perturbed upon binding of the spiking ligands, which serves as a possible explanation for reduced interface stability.