eprintid: 22344
rev_number: 12
eprint_status: archive
userid: 1589
dir: disk0/00/02/23/44
datestamp: 2016-12-15 13:44:24
lastmod: 2024-03-10 21:24:23
status_changed: 2016-12-15 13:44:24
type: article
metadata_visibility: show
creators_name: Kiani, Farooq Ahmad
creators_name: Fischer, Stefan
title: Effects of protonation on the hydrolysis of triphosphate in vacuum and the implications for catalysis by nucleotide hydrolyzing enzymes
subjects: 540
subjects: 570
divisions: 708000
abstract: Background: Nucleoside triphosphate (NTP) hydrolysis is a key reaction in biology. It involves breaking two very stable bonds (one P–O bond and one O–H bond of water), in either a concurrent or a sequential way. Here, we systematically examine how protonation of the triphosphate affects the mechanism of hydrolysis.   Results: The hydrolysis reaction of methyl triphosphate in vacuum is computed with protons in various numbers and position on the three phosphate groups. Protonation is seen to have a strong catalytic effect, with the reaction mechanism depending highly on the protonation pattern.   Conclusion: This dependence is apparently complicated, but is shown to obey a well-defined set of rules: Protonation of the α- and β-phosphate groups favors a sequential hydrolysis mechanism, whereas γ-protonation favors a concurrent mechanism, the two effects competing with each other in cases of simultaneous protonation. The rate-limiting step is always the breakup of the water molecule while it attacks the γ-phosphorus, and its barrier is lowered by γ-protonation. This step has significantly lower barriers in the sequential reactions, because the dissociated γ-metaphosphate intermediate (PγO3 −) is a much better target for water attack than the un-dissociated γ-phosphate (−PγO4 2−). The simple chemical logic behind these rules helps to better understand the catalytic strategy used by NTPase enzymes, as illustrated here for the catalytic pocket of myosin. A set of rules was determined that describes how protonating the phosphate groups affects the hydrolysis mechanism of methyl triphosphate: Protonation of the α- and/or β- phosphate groups promotes a sequential mechanism in which P-O bond breaking precedes the breakup of the attacking water, whereas protonation of the γ-phosphate promotes a concurrent mechanism and lowers the rate-limiting barrier of water breakup. The role played by individual protein residues in the catalytic pocket of triphosphate hydrolysing enzymes can be assigned accordingly.
date: 2016
publisher: BioMed Central; Springer
id_scheme: DOI
ppn_swb: 1655722670
own_urn: urn:nbn:de:bsz:16-heidok-223444
language: eng
bibsort: KIANIFAROOEFFECTSOFP2016
full_text_status: public
publication: BMC Biochemistry
volume: 17
number: 12
place_of_pub: London; Berlin; Heidelberg
pagerange: 1-13
issn: 1471-2091
citation:   Kiani, Farooq Ahmad ; Fischer, Stefan  (2016) Effects of protonation on the hydrolysis of triphosphate in vacuum and the implications for catalysis by nucleotide hydrolyzing enzymes.  BMC Biochemistry, 17 (12).  pp. 1-13.  ISSN 1471-2091     
document_url: https://archiv.ub.uni-heidelberg.de/volltextserver/22344/1/12858_2016_Article_68.pdf