4EAM

1.70A resolution structure of apo beta-glycosidase (W33G) from sulfolobus solfataricus

4EAM の概要

• エントリーDOI: 10.2210/pdb4eam/pdb
• 関連するPDBエントリー: 4EAN
• 分子名称: Beta-galactosidase, CHLORIDE ION, (4S)-2-METHYL-2,4-PENTANEDIOL, ... (5 entities in total)
• 機能のキーワード: glycoside hydrolase, chemical biology, allosteric activation, switchable enzyme, chemical rescue, hydrolase
• 由来する生物種: Sulfolobus solfataricus P2
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 114426.51

構造登録者

Lovell, S.,Battaile, K.P.,Deckert, K.,Brunner, L.C.,Budiardjo, S.J.,Karanicolas, J. (登録日: 2012-03-22, 公開日: 2012-06-13, 最終更新日: 2023-09-13)

主引用文献

Deckert, K.,Budiardjo, S.J.,Brunner, L.C.,Lovell, S.,Karanicolas, J.
Designing allosteric control into enzymes by chemical rescue of structure.
J.Am.Chem.Soc., 134:10055-10060, 2012

PubMed Abstract: Ligand-dependent activity has been engineered into enzymes for purposes ranging from controlling cell morphology to reprogramming cellular signaling pathways. Where these successes have typically fused a naturally allosteric domain to the enzyme of interest, here we instead demonstrate an approach for designing a de novo allosteric effector site directly into the catalytic domain of an enzyme. This approach is distinct from traditional chemical rescue of enzymes in that it relies on disruption and restoration of structure, rather than active site chemistry, as a means to achieve modulate function. We present two examples, W33G in a β-glycosidase enzyme (β-gly) and W492G in a β-glucuronidase enzyme (β-gluc), in which we engineer indole-dependent activity into enzymes by removing a buried tryptophan side chain that serves as a buttress for the active site architecture. In both cases, we observe a loss of function, and in both cases we find that the subsequent addition of indole can be used to restore activity. Through a detailed analysis of β-gly W33G kinetics, we demonstrate that this rescued enzyme is fully functionally equivalent to the corresponding wild-type enzyme. We then present the apo and indole-bound crystal structures of β-gly W33G, which together establish the structural basis for enzyme inactivation and rescue. Finally, we use this designed switch to modulate β-glycosidase activity in living cells using indole. Disruption and recovery of protein structure may represent a general technique for introducing allosteric control into enzymes, and thus may serve as a starting point for building a variety of bioswitches and sensors.

PubMed: 22655749
DOI: 10.1021/ja301409g

実験手法

X-RAY DIFFRACTION (1.7 Å)