[en] Background: Thiamine diphosphate (ThDP), an indispensable cofactor for oxidative energy metabolism, is syn- thesized through the reaction thiamine + ATP ⇆ ThDP + AMP, catalyzed by thiamine pyrophosphokinase 1 (TPK1), a cytosolic dimeric enzyme. It was claimed that the equilibrium of the reaction is in favor of the for- mation of thiamine and ATP, at odds with thermodynamic calculations. Here we show that this discrepancy is due to feedback inhibition by the product ThDP.
Methods: We used a purified recombinant mouse TPK1 to study reaction kinetics in the forward (physiological) and for the first time also in the reverse direction.
Results: Keq values reported previously are strongly underestimated, due to the fact the reaction in the forward direction rapidly slows down and reaches a pseudo-equilibrium as ThDP accumulates. We found that ThDP is a potent non-competitive inhibitor (Ki ≈ 0.4 μM) of the forward reaction. In the reverse direction, a true equi- librium is reached with a Keq of about 2 × 10− 5, strongly in favor of ThDP formation. In the reverse direction, we found a very low Km for ThDP (0.05 μM), in agreement with a tight binding of ThDP to the enzyme.
General significance: Inhibition of TPK1 by ThDP explains why intracellular ThDP levels remain low after administration of even very high doses of thiamine. Understanding the consequences of this feedback inhibition is essential for developing reliable methods for measuring TPK activity in tissue extracts and for optimizing the therapeutic use of thiamine and its prodrugs with higher bioavailability under pathological conditions.
Research Center/Unit :
Giga-Neurosciences - ULiège
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Sambon, Margaux
Pavlova, Oleksandra
Alhama-Riba, Judit
Wins, Pierre
Brans, Alain ; Université de Liège - ULiège > Département des sciences de la vie > Centre d'ingénierie des protéines
F.R.S.-FNRS - Fonds de la Recherche Scientifique FRIA - Fonds pour la Formation à la Recherche dans l'Industrie et dans l'Agriculture Erasmus+ Fonds Léon Fredericq
Funding text :
Experimental Scholarship for Central & Eastern Europe from the FEBS
scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.
Hasnain, G., Roje, S., Sa, N., Zallot, R., Ziemak, M.J., de Crécy-Lagard, V., Gregory, J.F., Hanson, A.D., Bacterial and plant HAD enzymes catalyse a missing phosphatase step in thiamin diphosphate biosynthesis. Biochem. J. 473 (2016), 157–166.
Kaziro, Y., Tanaka, R., Mano, Y., Shimazono, N., On the mechanism of transpyrophosphorylation in the biosynthesis of thiamine diphosphate. J. Biochem. Tokyo 49 (1961), 472–476.
Thomé-Beau, F., Lan, L.Thi, Olomucki, A., Thoai, N.Van, ATP:thiamine pyrophosphotransferase Purification and a study of the reaction mechanism. Biochim. Biophys. Acta 185 (1969), 111–121.
Mano, Y., Studies on enzymatic synthesis of cocarboxylase in animal tissue III purification and properties of thiaminokinase from rat liver. J. Biochem. Tokyo 47 (1960), 283–289.
Johnson, L.R., Gubler, C.J., Studies on the physiological functions of thiamine 3 the phosphorylation of thiamine in brain. Biochim. Biophys. Acta 156 (1968), 85–96.
Mitsuda, H., Takii, Y., Iwami, K., Yasumoto, K., Purification and properties of thiamine pyrophosphokinase from parsley leaf. J. Nutr. Sci. Vitaminol. (Tokyo) 21 (1975), 103–115.
Sanemori, H., Kawasaki, T., Purification and properties of thiamine pyrophosphokinase in paracoccus denitrificans. J. Biochem. Tokyo 88 (1980), 223–230.
Peterson, J.W., Gubler, C.J., Kuby, S.A., Partial purification and properties of thiamine pyrophosphokinase from pig brain. Biochim. Biophys. Acta 397 (1975), 377–394.
Onozuka, M., Nosaka, K., Steady-state kinetics and mutational studies of recombinant human thiamin pyrophosphokinase. J. Nutr. Sci. Vitaminol. Tokyo 49 (2003), 156–162.
Voskoboyev, A.I., Ostrovsky, Y.M., Thiamin pyrophosphokinase: structure, properties, and role in thiamin metabolism. Ann. N. Acad. Sci. 378 (1982), 161–176.
Artsukevich, I.M., Nucleotide specificity of rat liver thiamine pyrophosphokinase. Biokhimiya Mosc. 44 (1979), 543–547.
Nosaka, K., Kaneko, Y., Nishimura, H., Iwashima, A., Isolation and characterization of a thiamin pyrophosphokinase gene, THI80, from Saccharomyces cerevisiae. J. Biol. Chem. 268 (1993), 17440–17447.
Nosaka, K., Onozuka, M., Nishino, H., Nishimura, H., Kawasaki, Y., Ueyama, H., Molecular cloning and expression of a mouse thiamin pyrophosphokinase cDNA. J. Biol. Chem. 274 (1999), 34129–34133.
Bellyei, S., Szigeti, A., Boronkai, A., Szabo, Z., Bene, J., Janaky, T., Barna, L., Sipos, K., Minik, O., Kravjak, A., Ohmacht, R., Melegh, B., Zavodszky, P., Than, G.N., Sumegi, B., Bohn, H., Than, N.G., Cloning, sequencing, structural and molecular biological characterization of placental protein 20(PP20)/human thiamin pyrophosphokinase (hTPK). Placenta 26 (2005), 34–46.
Baker, L.J., Dorocke, J.A., Harris, R.A., Timm, D.E., The crystal structure of yeast thiamin pyrophosphokinase. Structure 9 (2001), 539–546.
Timm, D.E., Liu, J.Y., Baker, L.J., Harris, R.A., Crystal structure of thiamin pyrophosphokinase. J. Mol. Biol. 310 (2001), 195–204.
Liu, J.Y., Timm, D.E., Hurley, T.D., Pyrithiamine as a substrate for thiamine pyrophosphokinase. J. Biol. Chem. 281 (2006), 6601–6607.
Mitsuda, H., Takii, Y., Iwami, K., Yasumoto, K., Mechanism and regulation of thiamine pyrophosphokinase from parsley leaf. J. Nutr. Sci. Vitaminol. (Tokyo) 21 (1975), 189–198.
Ajjawi, I., Rodriguez Milla, M.A., Cushman, J., Shintani, D.K., Thiamin pyrophosphokinase is required for thiamin cofactor activation in arabidopsis. Plant Mol. Biol. 65 (2007), 151–162.
Nosaka, K., Onozuka, M., Kakazu, N., Hibi, S., Nishimura, H., Nishino, H., Abe, T., Isolation and characterization of a human thiamine pyrophosphokinase cDNA. Biochim. Biophys. Acta 1517 (2001), 293–297.
Rüsch, C.T., Wortmann, S.B., Kovacs-Nagy, R., Grehten, P., Häberle, J., Latal, B., Stettner, G.M., Thiamine pyrophosphokinase deficiency due to mutations in the TPK1 gene: a rare, treatable neurodegenerative disorder. Neuropediatrics 52 (2021), 126–132.
Eckenweiler, M., Mayr, J.A., Grünert, S., Abicht, A., Korinthenberg, R., Thiamine treatment and favorable outcome in an infant with biallelic TPK1 variants. Neuropediatrics 52 (2020), 123–125.
Mayr, J.A., Freisinger, P., Schlachter, K., Rolinski, B., Zimmermann, F.A., Scheffner, T., Haack, T.B., Koch, J., Ahting, U., Prokisch, H., Sperl, W., Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway. Am. J. Hum. Genet. 89 (2011), 806–812.
Fraser, J.L., Vanderver, A., Yang, S., Chang, T., Cramp, L., Vezina, G., Lichter-Konecki, U., Cusmano-Ozog, K.P., Smpokou, P., Chapman, K.A., Zand, D.J., Thiamine pyrophosphokinase deficiency causes a Leigh disease like phenotype in a sibling pair: identification through whole exome sequencing and management strategies. Mol. Genet. Metab. Rep. 1 (2014), 66–70.
Marcé-Grau, A., Martí-Sánchez, L., Baide-Mairena, H., Ortigoza-Escobar, J.D., Pérez-Dueñas, B., Genetic defects of thiamine transport and metabolism: a review of clinical phenotypes, genetics, and functional studies. J. Inherit. Metab. Dis. 42 (2019), 581–597.
Banka, S., de Goede, C., Yue, W.W., Morris, A.A., von Bremen, B., Chandler, K.E., Feichtinger, R.G., Hart, C., Khan, N., Lunzer, V., Matakovic, L., Marquardt, T., Makowski, C., Prokisch, H., Debus, O., Nosaka, K., Sonwalkar, H., Zimmermann, F.A., Sperl, W., Mayr, J.A., Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations. Mol. Genet. Metab. 113 (2014), 301–306.
Bugiardini, E., Pope, S., Feichtinger, R.G., Poole, O.V., Pittman, A.M., Woodward, C.E., Heales, S., Quinlivan, R., Houlden, H., Mayr, J.A., Hanna, M.G., Pitceathly, R.D.S., Utility of whole blood thiamine pyrophosphate evaluation in TPK1-related diseases. J. Clin. Med., 8, 2019, 991.
Zhu, B., Wu, J., Chen, G., Chen, L., Yao, Y., Whole exome sequencing identifies a novel mutation of TPK1 in a chinese family with recurrent ataxia. J. Mol. Neurosci. 70 (2020), 1237–1243.
Peterson, G.L., A simplification of the protein assay method of Lowry et al. which is more generally applicable. Anal. Biochem. 83 (1977), 346–356.
Bettendorff, L., Mastrogiacomo, F., Kish, S.J., Grisar, T., Thiamine, thiamine phosphates, and their metabolizing enzymes in human brain. J. Neurochem. 66 (1996), 250–258.
Bettendorff, L., Peeters, M., Jouan, C., Wins, P., Schoffeniels, E., Determination of thiamin and its phosphate esters in cultured neurons and astrocytes using an ion-pair reversed-phase high-performance liquid chromatographic method. Anal. Biochem. 198 (1991), 52–59.
Gangolf, M., Wins, P., Thiry, M., El Moualij, B., Bettendorff, L., Thiamine triphosphate synthesis in rat brain occurs in mitochondria and is coupled to the respiratory chain. J. Biol. Chem. 285 (2010), 583–594.
Bettendorff, L., Goessens, G., Sluse, F., Wins, P., Bureau, M., Laschet, J., Grisar, T., Thiamine deficiency in cultured neuroblastoma cells: effect on mitochondrial function and peripheral benzodiazepine receptors. J. Neurochem. 64 (1995), 2013–2021.
Sambon, M., Napp, A., Demelenne, A., Vignisse, J., Wins, P., Fillet, M., Bettendorff, L., Thiamine and benfotiamine protect neuroblastoma cells against paraquat and β-amyloid toxicity by a coenzyme-independent mechanism. Heliyon, 5, 2019, e01710.
O'Sullivan, W.J., Smithers, G.W., Stability constants for biologically important metal-ligand complexes. Methods Enzymol. 63 (1979), 294–336.
Veloso, D., Guynn, R.W., Oskarsson, M., Veech, R.L., The concentrations of free and bound magnesium in rat tissues relative constancy of free mg 2+ concentrations. J. Biol. Chem. 248 (1973), 4811–4819.
Schoenmakers, T.J., Visser, G.J., Flik, G., Theuvenet, A.P., CHELATOR: an improved method for computing metal ion concentrations in physiological solutions. BioTechniques 12:870–874 (1992), 876–879.
Voet, D., Voet, J.G., Pratt, C.W., Principles of Biochemistry. 2013, John Wiley & Sons, Singapore.
Makarchikov, A.F., Lakaye, B., Gulyai, I.E., Czerniecki, J., Coumans, B., Wins, P., Grisar, T., Bettendorff, L., Thiamine triphosphate and thiamine triphosphatase activities: from bacteria to mammals. Cell. Mol. Life Sci. 60 (2003), 1477–1488.
Barchi, R.L., Viale, R.O., Membrane-associated thiamin triphosphatase II activation by divalent cations. J. Biol. Chem. 251 (1976), 193–197.
Volvert, M.L., Seyen, S., Piette, M., Evrard, B., Gangolf, M., Plumier, J.C., Bettendorff, L., Benfotiamine, a synthetic S-acyl thiamine derivative, has different mechanisms of action and a different pharmacological profile than lipid-soluble thiamine disulfide derivatives. BMC Pharmacol., 8, 2008, 10.
Sambon, M., Gorlova, A., Demelenne, A., Alhama-Riba, J., Coumans, B., Lakaye, B., Wins, P., Fillet, M., Anthony, D.C., Strekalova, T., Bettendorff, L., Dibenzoylthiamine has powerful antioxidant and anti-inflammatory properties in cultured cells and in mouse models of stress and neurodegeneration. Biomedicines, 8, 2020, 361.
Bettendorff, L., The compartmentation of phosphorylated thiamine derivatives in cultured neuroblastoma cells. Biochim. Biophys. Acta 1222 (1994), 7–14.
Bettendorff, L., Wins, P., Lesourd, M., Subcellular localization and compartmentation of thiamine derivatives in rat brain. Biochim. Biophys. Acta 1222 (1994), 1–6.
Casirola, D., Patrini, C., Ferrari, G., Rindi, G., Thiamin transport by human erythrocytes and ghosts. J. Membr. Biol. 118 (1990), 11–18.
Bettendorff, L., Wins, P., Mechanism of thiamine transport in neuroblastoma cells inhibition of a high affinity carrier by sodium channel activators and dependence of thiamine uptake on membrane potential and intracellular ATP. J. Biol. Chem. 269 (1994), 14379–14385.
Wakabayashi, Y., Iwashima, A., Nose, Y., Affinity chromatography of thiamin pyrophosphokinase of rat brain. Biochim. Biophys. Acta 429 (1976), 1085–1087.
Switzer, R.L., Regulation and mechanism of phosphoribosylpyrophosphate synthetase I purification and properties of the enzyme from salmonella typhimurium. J. Biol. Chem. 244 (1969), 2854–2863.
Yoshioka, H., Nishino, K., Miyake, T., Ohshio, G., Kimura, T., Hamashima, Y., Immunohistochemical localization of a new thiamine diphosphate-binding protein in the rat nervous system. Neurosci. Lett. 77 (1987), 10–14.
Neet, K.E., Cooperativity in enzyme function: equilibrium and kinetic aspects. Methods Enzymol. 249 (1995), 519–567.
Artsukevich, I.M., Voskoboev, A.I., Ostrovskii, I.U.M., Purification and several properties of thiamine pyrophosphokinase from rat liver. Vopr. Med. Khim 23 (1977), 203–210.
Molin, W.T., Fites, R.C., Isolation and characterization of thiamin pyrophosphotransferase from Glycine max seedlings. Plant Physiol. 66 (1980), 308–312.
Rapala-Kozik, M., Golda, A., Kujda, M., Enzymes that control the thiamine diphosphate pool in plant tissues properties of thiamine pyrophosphokinase and thiamine-(di)phosphate phosphatase purified from zea mays seedlings. Plant Physiol. Biochem. 47 (2009), 237–242.
Liu, J.Y., Hurley, T.D., A new crystal form of mouse thiamin pyrophosphokinase. Int. J. Biochem. Mol. Biol. 2 (2011), 111–118.
Xie, F., Cheng, Z., Li, S., Liu, X., Guo, X., Yu, P., Gu, Z., Pharmacokinetic study of benfotiamine and the bioavailability assessment compared to thiamine hydrochloride. J. Clin. Pharmacol. 54 (2014), 688–695.
Gibson, G.E., Luchsinger, J.A., Cirio, R., Chen, H., Franchino-Elder, J., Hirsch, J.A., Bettendorff, L., Chen, Z., Flowers, S., Gerber, L., Grandville, T., Schupf, N., Xu, H., Stern, Y., Habeck, C., Jordan, B., Fonzetti, P., Benfotiamine and cognitive decline in Alzheimer's disease: results of a randomized placebo-controlled phase IIa clinical trial. J. Alzheimers Dis. 78 (2020), 989–1010.
Sheng, L., Cao, W., Lin, P., Chen, W., Xu, H., Zhong, C., Yuan, F., Chen, H., Li, H., Liu, C., Yang, M., Li, X., Safety, tolerability and pharmacokinetics of single and multiple ascending doses of benfotiamine in healthy subjects. Drug Des. Devel. Ther. 15 (2021), 1101–1110.
Gangolf, M., Czerniecki, J., Radermecker, M., Detry, O., Nisolle, M., Jouan, C., Martin, D., Chantraine, F., Lakaye, B., Wins, P., Grisar, T., Bettendorff, L., Thiamine status in humans and content of phosphorylated thiamine derivatives in biopsies and cultured cells. PLoS One, 5, 2010, e13616.
Similar publications
Sorry the service is unavailable at the moment. Please try again later.
This website uses cookies to improve user experience. Read more
Save & Close
Accept all
Decline all
Show detailsHide details
Cookie declaration
About cookies
Strictly necessary
Performance
Strictly necessary cookies allow core website functionality such as user login and account management. The website cannot be used properly without strictly necessary cookies.
This cookie is used by Cookie-Script.com service to remember visitor cookie consent preferences. It is necessary for Cookie-Script.com cookie banner to work properly.
Performance cookies are used to see how visitors use the website, eg. analytics cookies. Those cookies cannot be used to directly identify a certain visitor.
Used to store the attribution information, the referrer initially used to visit the website
Cookies are small text files that are placed on your computer by websites that you visit. Websites use cookies to help users navigate efficiently and perform certain functions. Cookies that are required for the website to operate properly are allowed to be set without your permission. All other cookies need to be approved before they can be set in the browser.
You can change your consent to cookie usage at any time on our Privacy Policy page.