Tautomerism of histidine 64 associated with proton transfer in catalysis of carbonic anhydrase. 2007

Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
Center for Nano Materials and Technology, Japan Advanced Institute of Science and Technology, Nomi, Ishikawa 923-1211; Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871; Institute for Protein Research, Osaka University, Suita, Osaka 565-0871; Osaka University of Pharmaceutical Sciences, Takatsuki, Osaka 569-1094, Japan.

The imidazole (15)N signals of histidine 64 (His(64)), involved in the catalytic function of human carbonic anhydrase II (hCAII), were assigned unambiguously. This was accomplished by incorporating the labeled histidine as probes for solution NMR analysis, with (15)N at ring-N(delta1) and N(epsilon2), (13)Cat ring-Cepsilon1, (13)C and (15)N at all carbon and nitrogen, or (15)N at the amide nitrogen and the labeled glycine with (13)C at the carbonyl carbon. Using the pH dependence of ring-(15)N signals and a comparison between experimental and simulated curves, we determined that the tautomeric equilibrium constant (K(T)) of His(64) is 1.0, which differs from that of other histidine residues. This unique value characterizes the imidazole nitrogen atoms of His(64) as both a general acid (a) and base (b): its epsilon2-nitrogen as (a) releases one proton into the bulk, whereas its delta1-nitrogen as (b) extracts another proton from a water molecule within the water bridge coupling to the zinc-bound water inside the cave. This accelerates the generation of zinc-bound hydroxide to react with the carbon dioxide. Releasing the productive bicarbonate ion from the inside separates the water bridge pathway, in which the next water molecules move into beside zinc ion. A new water molecule is supplied from the bulk to near the delta1-nitrogen of His(64). These reconstitute the water bridge. Based on these features, we suggest here a catalytic mechanism for hCAII: the tautomerization of His(64) can mediate the transfers of both protons and water molecules at a neutral pH with high efficiency, requiring no time- or energy-consuming processes.

UI MeSH Term Description Entries
D007536 Isomerism The phenomenon whereby certain chemical compounds have structures that are different although the compounds possess the same elemental composition. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Isomerisms
D011522 Protons Stable elementary particles having the smallest known positive charge, found in the nuclei of all elements. The proton mass is less than that of a neutron. A proton is the nucleus of the light hydrogen atom, i.e., the hydrogen ion. Hydrogen Ions,Hydrogen Ion,Ion, Hydrogen,Ions, Hydrogen,Proton
D002256 Carbonic Anhydrases A family of zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide. They play an important role in the transport of CARBON DIOXIDE from the tissues to the LUNG. EC 4.2.1.1. Carbonate Dehydratase,Carbonic Anhydrase,Anhydrases, Carbonic,Dehydratase, Carbonate
D002384 Catalysis The facilitation of a chemical reaction by material (catalyst) that is not consumed by the reaction. Catalyses
D004735 Energy Transfer The transfer of energy of a given form among different scales of motion. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed). It includes the transfer of kinetic energy and the transfer of chemical energy. The transfer of chemical energy from one molecule to another depends on proximity of molecules so it is often used as in techniques to measure distance such as the use of FORSTER RESONANCE ENERGY TRANSFER. Transfer, Energy
D004926 Escherichia coli A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc. Alkalescens-Dispar Group,Bacillus coli,Bacterium coli,Bacterium coli commune,Diffusely Adherent Escherichia coli,E coli,EAggEC,Enteroaggregative Escherichia coli,Enterococcus coli,Diffusely Adherent E. coli,Enteroaggregative E. coli,Enteroinvasive E. coli,Enteroinvasive Escherichia coli
D006639 Histidine An essential amino acid that is required for the production of HISTAMINE. Histidine, L-isomer,L-Histidine,Histidine, L isomer,L-isomer Histidine
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006863 Hydrogen-Ion Concentration The normality of a solution with respect to HYDROGEN ions; H+. It is related to acidity measurements in most cases by pH pH,Concentration, Hydrogen-Ion,Concentrations, Hydrogen-Ion,Hydrogen Ion Concentration,Hydrogen-Ion Concentrations
D001665 Binding Sites The parts of a macromolecule that directly participate in its specific combination with another molecule. Combining Site,Binding Site,Combining Sites,Site, Binding,Site, Combining,Sites, Binding,Sites, Combining

Related Publications

Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
November 1988, Biochemistry,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
August 2007, Accounts of chemical research,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
August 1992, Biochimica et biophysica acta,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
February 2010, Biochimica et biophysica acta,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
July 1990, Biochemistry,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
May 2005, Archives of biochemistry and biophysics,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
January 1999, Archives of biochemistry and biophysics,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
August 2006, Biopolymers,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
January 2013, Biochemistry,
Hideto Shimahara, and Takuya Yoshida, and Yasutaka Shibata, and Masato Shimizu, and Yoshimasa Kyogoku, and Fumio Sakiyama, and Takashi Nakazawa, and Shin-Ichi Tate, and Shin-Ya Ohki, and Takeshi Kato, and Hozumi Moriyama, and Ken-Ichi Kishida, and Yasuo Tano, and Tadayasu Ohkubo, and Yuji Kobayashi
May 1998, Biochemistry,
Copied contents to your clipboard!