Ribonuclease A Catalysis: Difference between revisions
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[[Image:RNaseAII.PNG|300px|left|thumb|Figure I: Bovine Ribonuclease A. Colored residues are representative of amino acids important to both the acid base catalysis (Red: His12 and 119) and stabilization of the transition state (Blue: Lys41 and Phe120). Figure generated via ''Pymol'' ]] | [[Image:RNaseAII.PNG|300px|left|thumb|Figure I: Bovine Ribonuclease A. Colored residues are representative of amino acids important to both the acid base catalysis (Red: His12 and 119) and stabilization of the transition state (Blue: Lys41 and Phe120). Figure generated via ''Pymol'' ]] | ||
{{STRUCTURE_7rsa | PDB=7RSA | SCENE= | |||
{{STRUCTURE_7rsa | PDB=7RSA | SCENE= Sandbox_Reserved_193/His12/1 }} | |||
===Acid Base Catalysis=== | ===Acid Base Catalysis=== | ||
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| This Sandbox is Reserved from Feb 02, 2011, through Jul 31, 2011 for use by the Biochemistry II class at the Butler University at Indianapolis, IN USA taught by R. Jeremy Johnson. This reservation includes Sandbox Reserved 191 through Sandbox Reserved 200. |
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Ribonuclease A CatalysisRibonuclease A Catalysis
IntroductionIntroduction
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| 7rsa, resolution 1.26Å () | |||||||||
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| Ligands: | , | ||||||||
| Activity: | Pancreatic ribonuclease, with EC number 3.1.27.5 | ||||||||
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| Resources: | FirstGlance, OCA, RCSB, PDBsum | ||||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||||
Acid Base CatalysisAcid Base Catalysis
In organic chemistry acid/base catalysis is the addition of an acid or base to accelerate a chemical reaction. Ribonuclease A, (RNase A), also uses acid/base catatalysis to chemically change its substrates. Acidic or basic residues of the enzyme transfer protons to or from the reactant in order to stabilize the developing charges in the transition state. The transfer of protons usually creates better leaving groups, making the reaction more energetically favorable. Histidine is a very common amino acid residue involved in cataylsis, as histidine has a pKa value close to neutral, (pKa=6); therefore, histidine can both accept and donate protons at physiological pH.
Acid/base catalysis by an enzyme is dependent on the pH of the environment and the pKa's of their residues. The pKa value will increase for an acidic residue if the environment is hydrophobic or if the adjacent residues are of similar charges. In the same environmental conditions, a basic residue will decrease the pKa. Having the ability to alter the pKa of certain residues such as Histidine, increases the diversity of reactions that can take place (reword).
Active Site StructureActive Site Structure
RNase A uses acid/base catlysis to speed up RNA hydrolysis. This occurs in the active site which is found in the cleft of RNase A and is the location of the chemical change in bound substrates. Subsites lining the active site cleft are important to the binding of single stranded RNA. Large quantities of positively charged residues, such as Lys7 and Lys66 and Arg10, recognize the negative charge on the phosphate back bone of the RNA strand.
The active site for RNase A, although fairly nonspecific, has some specificity for sites RNA hydrolysis. Threonine 45, located next to the active site, will hydrogen bond to pyrimidine bases, but sterically hinder the binding of a purine on the 5' strand of OH. Thr45 significantly decreases the rate of hydrolysis of polymeric purine strands, such as poly A, by a thousand fold, as compared to polymeric pyrimidine strands.
Early studies on RNase A catalysis showed that alkylation of His12 and His119 significantly decreased its catalytic activity, prompting the hypothesis that these two histidines were the acid/base catalyst. Confirmation of this hypothesis came when these histidines were replaced with alanine and the reaction rates of either mutation dropped by ten-thousand fold.
Acid Base Catalysis by RNase AAcid Base Catalysis by RNase A
MechanismMechanism
catalyzes the cleavage of the Phosphodiester bonds in two steps: the formation of the pentavalent phosphate transition state and subsequent degradation of the 2’3’ cyclic phosphate intermediate. An important part of the reaction is the ability of histidine (His 12 and His119) to both accept and donate electrons, allowing these histidine to be an acid or a base, making the reaction pH dependent.
RNA hydrolysis begins when abstracts a proton from the 2’ OH group on RNA; thus, assisting in the nucleophilic attack of the 2’ oxygen on the electrophilic phosphorus atom. A transition state is then formed, having a pentavalent phosphate, which is stabilized by the positively charged amino group of and the main chain amide nitrogen of Phe120. then protonates the 5' oxygen on the ribose ring and the transition state falls to form a 2’3’cyclic phosphate intermediate.
In a secondary and separate reaction, the 2’,3’ cyclic phosphate is hydrolyzed to a mixture of 2'phosphate and 3' hydroxyl. His12 donates a proton to the leaving group of this reaction, the 3’ oxygen of the cyclic intermediate. Simultaneously, His-119 abstracts the proton from a water molecule, activating it for nucleophilic attack. The activated water molecule attacks the cyclic phosphate causing the cleavage of the 2'3’ cyclic phosphate intermediate. The truncated nucleotide is then released with a 3’ phosphate group.
InhibitorsInhibitors
Due to the highly catalytic nature of RNase A for RNA strands, mammalian cells have developed a protective inhibitor to prevent pancreatic ribonucleases from degrading cystolic RNA. Ribonuclease Inhibitor (RI) tightly associates to the active site due to its non-globular nature. I am waiting for a paper from nature that is pertinant to RIs. If any have to due with inhibition at the active site I thought this would be a good place to add. This is what I could get from the abstract.
Related SitesRelated Sites
Works CitedWorks Cited
1.Raines, R. Ribonuclease A. Chemistry Review: (1998) Vol. 98 pp. 1045-1068
2.Wlodrawer, A., Svensson, L., Sjohin, L., Gilliland, G. Structure of Phosphate-Free Ribonuclease A Refined at 1.26A. Biochemistry:(1988) Vol. 27 pp. 2705-2717