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Essential Functional Interplay of the Catalytic Groups in Acid Phosphatase

Pfeiffer, Martin (författare)
Graz Univ Technol, Inst Biotechnol & Biochem Engn, A-8010 Graz, Austria.;Austrian Ctr Ind Biotechnol, A-8010 Graz, Austria.
Crean, Rory M. (författare)
Uppsala universitet,Biokemi,Science for Life Laboratory, SciLifeLab
Moreira, Catia (författare)
Uppsala universitet,Biokemi,Science for Life Laboratory, SciLifeLab
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Parracino, Antonietta (författare)
Uppsala universitet,Biokemi,Science for Life Laboratory, SciLifeLab
Oberdorfer, Gustav (författare)
Graz Univ Technol, Inst Biochem, A-8010 Graz, Austria.
Brecker, Lothar (författare)
Univ Vienna, Dept Organ Chem, A-1090 Vienna, Austria.
Hammerschmidt, Friedrich (författare)
Univ Vienna, Dept Organ Chem, A-1090 Vienna, Austria.
Kamerlin, Shina C. Lynn, 1981- (författare)
Uppsala universitet,Biokemi
Nidetzky, Bernd (författare)
Graz Univ Technol, Inst Biotechnol & Biochem Engn, A-8010 Graz, Austria.;Austrian Ctr Ind Biotechnol, A-8010 Graz, Austria.
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Graz Univ Technol, Inst Biotechnol & Biochem Engn, A-8010 Graz, Austria;Austrian Ctr Ind Biotechnol, A-8010 Graz, Austria. Biokemi (creator_code:org_t)
2022-02-28
2022
Engelska.
Ingår i: ACS Catalysis. - : American Chemical Society (ACS). - 2155-5435 .- 2155-5435. ; 12:6, s. 3357-3370
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The cooperative interplay between the functional devices of a preorganized active site is fundamental to enzyme catalysis. An in-depth understanding of this phenomenon is central to elucidating the remarkable efficiency of natural enzymes and provides an essential benchmark for enzyme design and engineering. Here, we study the functional interconnectedness of the catalytic nucleophile (His18) in an acid phosphatase by analyzing the consequences of its replacement with aspartate. We present crystallographic, biochemical, and computational evidence for a conserved mechanistic pathway via a phospho-enzyme intermediate on Asp18. Linear free-energy relationships for phosphoryl transfer from phosphomonoester substrates to His18/Asp18 provide evidence for the cooperative interplay between the nucleophilic and general-acid catalytic groups in the wild-type enzyme, and its substantial loss in the H18D variant. As an isolated factor of phosphatase efficiency, the advantage of a histidine compared to an aspartate nucleophile is similar to 10(4)-fold. Cooperativity with the catalytic acid adds >= 10(2)-fold to that advantage. Empirical valence bond simulations of phosphoryl transfer from glucose 1-phosphate to His and Asp in the enzyme explain the loss of activity of the Asp18 enzyme through a combination of impaired substrate positioning in the Michaelis complex, as well as a shift from early to late protonation of the leaving group in the H18D variant. The evidence presented furthermore suggests that the cooperative nature of catalysis distinguishes the enzymatic reaction from the corresponding reaction in solution and is enabled by the electrostatic preorganization of the active site. Our results reveal sophisticated discrimination in multifunctional catalysis of a highly proficient phosphatase active site.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Biokatalys och enzymteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Biocatalysis and Enzyme Technology (hsv//eng)

Nyckelord

functional cooperativity
enzyme catalysis
EVB simulations
linear free-energy relationship
nucleophilic catalysis
phosphate transfer

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