Acid-base chemistry of frustrated water at protein interfaces

被引:1
|
作者
Fernandez, Ariel [1 ,2 ]
机构
[1] Natl Res Council CONICET, Argentine Inst Math IAM, RA-1083 Buenos Aires, DF, Argentina
[2] Coll Basilea, Inst Adv Study, Basel, Switzerland
关键词
anticontacts; hydrogen-bond frustration; interfacial physics; molecular biophysics; protein-water interface; structural biology; EGFR KINASE; ONCOGENIC MUTATIONS; RECOGNITION; MECHANISM; INSIGHTS; DOMAIN;
D O I
10.1002/1873-3468.12047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Water molecules at a protein interface are often frustrated in hydrogen-bonding opportunities due to subnanoscale confinement. As shown, this condition makes them behave as a general base that may titrate side-chain ammonium and guanidinium cations. Frustration-based chemistry is captured by a quantum mechanical treatment of proton transference and shown to remove same-charge uncompensated anticontacts at the interface found in the crystallographic record and in other spectroscopic information on the aqueous interface. Such observations are untenable within classical arguments, as hydronium is a stronger acid than ammonium or guanidinium. Frustration enables a directed Grotthuss mechanism for proton transference stabilizing same-charge anticontacts.
引用
收藏
页码:215 / 223
页数:9
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