Arginine: Its pKa value revisited

被引:296
作者
Fitch, Carolyn A. [1 ]
Platzer, Gerald [2 ,3 ]
Okon, Mark [2 ,3 ]
Garcia-Moreno E, Bertrand [1 ]
McIntosh, Lawrence P. [2 ,3 ]
机构
[1] Johns Hopkins Univ, Dept Biophys, Baltimore, MD 21218 USA
[2] Univ British Columbia, Dept Biochem & Mol Biol, Dept Chem, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Michael Smith Labs, Vancouver, BC V6T 1Z3, Canada
基金
奥地利科学基金会; 美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
protein electrostatics; pH titration; equilibrium acid dissociation constant; pKa value; guanidinium; tautomer; potentiometry; NMR spectroscopy; NUCLEAR-MAGNETIC-RESONANCE; APPARENT DISSOCIATION-CONSTANTS; N-15; CHEMICAL-SHIFTS; AMINO-ACIDS; NATURAL-ABUNDANCE; BACTERIORHODOPSIN PHOTOCYCLE; HYDROPHOBIC INTERIOR; IONIZABLE GROUPS; PROTON-TRANSFER; PH-DEPENDENCE;
D O I
10.1002/pro.2647
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
Using complementary approaches of potentiometry and NMR spectroscopy, we have determined that the equilibrium acid dissociation constant (pK(a) value) of the arginine guanidinium group is 13.8 +/- 0.1. This is substantially higher than that of approximate to 12 often used in structure-based electrostatics calculations and cited in biochemistry textbooks. The revised intrinsic pK(a) value helps explains why arginine side chains in proteins are always predominantly charged, even at pH values as great as 10. The high pK(a) value also reinforces the observation that arginine side chains are invariably protonated under physiological conditions of near neutral pH. This occurs even when the guanidinium moiety is buried in a hydrophobic micro-environment, such as that inside a protein or a lipid membrane, thought to be incompatible with the presence of a charged group.
引用
收藏
页码:752 / 761
页数:10
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