Hexokinase II explained

Hexokinase II, also known as Hexokinase B and HK2, is an enzyme which in humans is encoded by the HK2 gene on chromosome 2.[1] [2] Hexokinases phosphorylate glucose to produce glucose 6-phosphate, the first step in most glucose metabolism pathways. Hexokinase II is the predominant hexokinase form found in skeletal muscle. It localizes to the outer membrane of mitochondria. Expression of the HK2 gene is insulin-responsive, and studies in rat suggest that it is involved in the increased rate of glycolysis seen in rapidly growing cancer cells. [provided by RefSeq, Apr 2009][2]

Structure

Hexokinase II is one of four homologous hexokinase isoforms in mammalian cells.[3] [4] [5] [6] [7]

Gene

The HK2 gene spans approximately 50 kb and consists of 18 exons. There is also an HK2 pseudogene integrated into a long interspersed nuclear repetitive DNA element located on the X chromosome. Though its DNA sequence is similar to the cDNA product of the actual HK2 mRNA transcript, it lacks an open reading frame for gene expression.[6]

Protein

This gene encodes a 100-kDa, 917-residue enzyme with highly similar N-terminal and C-terminal domains that each form half of the protein.[6] [8] This high similarity, along with the existence of a 50-kDa hexokinase (HK4), suggests that the 100-kDa hexokinases originated from a 50-kDa precursor via gene duplication and tandem ligation.[6] [7] Both N- and C-terminal domains possess catalytic ability and can be inhibited by glucose 6-phosphate, though the C-terminal domain demonstrates lower affinity for ATP and is only inhibited at higher concentrations of glucose 6-phosphate.[6] Despite there being two binding sites for glucose, it is proposed that glucose binding at one site induces a conformational change which prevents a second glucose from binding the other site.[9] Meanwhile, the first 12 amino acids of the highly hydrophobic N-terminal serve to bind the enzyme to the mitochondria, while the first 18 amino acids contribute to the enzyme’s stability.[5] [7]

Function

As an isoform of hexokinase and a member of the sugar kinase family, hexokinase II catalyzes the rate-limiting and first obligatory step of glucose metabolism, which is the ATP-dependent phosphorylation of glucose to glucose 6-phosphate.[7] Physiological levels of glucose 6-phosphate can regulate this process by inhibiting hexokinase II as negative feedback, though inorganic phosphate (Pi) can relieve glucose 6-phosphate inhibition.[4] [6] [7] Pi can also directly regulate hexokinase II, and the double regulation may better suit its anabolic functions.[4] By phosphorylating glucose, hexokinase II effectively prevents glucose from leaving the cell and, thus, commits glucose to energy metabolism.[6] [8] Moreover, its localization and attachment to the OMM promotes the coupling of glycolysis to mitochondrial oxidative phosphorylation, which greatly enhances ATP production to meet the cell’s energy demands.[10] [11] Specifically, hexokinase II binds VDAC to trigger opening of the channel and release mitochondrial ATP to further fuel the glycolytic process.[4] [11]

Another critical function for OMM-bound hexokinase II is mediation of cell survival.[4] [5] Activation of Akt kinase maintains HK2-VDAC coupling, which subsequently prevents cytochrome c release and apoptosis, though the exact mechanism remains to be confirmed.[4] One model proposes that hexokinase II competes with the pro-apoptotic proteins BAX to bind VDAC, and in the absence of hexokinase II, BAX induces cytochrome c release.[4] [11] In fact, there is evidence that hexokinase II restricts BAX and BAK oligomerization and binding to the OMM. In a similar mechanism, the pro-apoptotic creatine kinase binds and opens VDAC in the absence of hexokinase II.[4] An alternative model proposes the opposite, that hexokinase II regulates binding of the anti-apoptotic protein Bcl-Xl to VDAC.[11]

In particular, hexokinase II is ubiquitously expressed in tissues, though it is majorly found in muscle and adipose tissue.[4] [6] [11] In cardiac and skeletal muscle, hexokinase II can be found bound to both the mitochondrial and sarcoplasmic membrane.[12] HK2 gene expression is regulated by a phosphatidylinositol 3-kinaselp70 S6 protein kinase-dependent pathway and can be induced by factors such as insulin, hypoxia, cold temperatures, and exercise.[6] [13] Its inducible expression indicates its adaptive role in metabolic responses to changes in the cellular environment.[13]

Clinical significance

Cancer

Hexokinase II is highly expressed in several cancers, including breast cancer and colon cancer.[5] [11] [14] Its role in coupling ATP from oxidative phosphorylation to the rate-limiting step of glycolysis may help drive the tumor cells’ growth.[11] Notably, inhibition of hexokinase II has demonstrably improved the effectiveness of anticancer drugs.,[14] Thus, hexokinase II stands as a promising therapeutic target, though considering its ubiquitous expression and crucial role in energy metabolism, a reduction rather than complete inhibition of its activity should be pursued.[11] [14]

Non-insulin-dependent diabetes mellitus

A study on non-insulin-dependent diabetes mellitus (NIDDM) revealed low basal glucose 6-phosphate levels in NIDDM patients that failed to increase with the addition of insulin. One possible cause is decreased phosphorylation of glucose due to a defect in hexokinase II, which was confirmed in further experiments. However, the study could not establish any links between NIDDM and mutations in the HK2 gene, indicating that the defect may lie in hexokinase II regulation.[6]

Interactions

HK2 is known to interact with:

See also

Further reading

Notes and References

  1. Lehto M, Xiang K, Stoffel M, Espinosa R, Groop LC, Le Beau MM, Bell GI . Human hexokinase II: localization of the polymorphic gene to chromosome 2 . Diabetologia . 36 . 12 . 1299–302 . Dec 1993 . 8307259 . 10.1007/BF00400809 . free .
  2. Web site: Entrez Gene: HK2 hexokinase 2 .
  3. Murakami K, Kanno H, Tancabelic J, Fujii H . Gene expression and biological significance of hexokinase in erythroid cells . Acta Haematologica . 108 . 4 . 204–9 . 2002 . 12432216 . 10.1159/000065656. 23521290 .
  4. Okatsu K, Iemura S, Koyano F, Go E, Kimura M, Natsume T, Tanaka K, Matsuda N . Mitochondrial hexokinase HKI is a novel substrate of the Parkin ubiquitin ligase . Biochemical and Biophysical Research Communications . 428 . 1 . 197–202 . Nov 2012 . 23068103 . 10.1016/j.bbrc.2012.10.041 .
  5. Schindler A, Foley E . Hexokinase 1 blocks apoptotic signals at the mitochondria . Cellular Signalling . 25 . 12 . 2685–92 . Dec 2013 . 24018046 . 10.1016/j.cellsig.2013.08.035 .
  6. Printz RL, Osawa H, Ardehali H, Koch S, Granner DK . Hexokinase II gene: structure, regulation and promoter organization . Biochemical Society Transactions . 25 . 1 . 107–12 . Feb 1997 . 9056853 . 10.1042/bst0250107.
  7. Ahn KJ, Kim J, Yun M, Park JH, Lee JD . Enzymatic properties of the N- and C-terminal halves of human hexokinase II . BMB Reports . 42 . 6 . 350–5 . Jun 2009 . 19558793 . 10.5483/bmbrep.2009.42.6.350. free .
  8. Aleshin AE, Zeng C, Bourenkov GP, Bartunik HD, Fromm HJ, Honzatko RB . The mechanism of regulation of hexokinase: new insights from the crystal structure of recombinant human brain hexokinase complexed with glucose and glucose-6-phosphate . Structure . 6 . 1 . 39–50 . Jan 1998 . 9493266 . 10.1016/s0969-2126(98)00006-9. free .
  9. Cárdenas. ML. Athel Cornish-Bowden. Cornish-Bowden. A. Ureta. T. Evolution and regulatory role of the hexokinases.. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 5 March 1998. 1401. 3. 242–64. 9540816. 10.1016/s0167-4889(97)00150-x. free.
  10. Shan D, Mount D, Moore S, Haroutunian V, Meador-Woodruff JH, McCullumsmith RE . Abnormal partitioning of hexokinase 1 suggests disruption of a glutamate transport protein complex in schizophrenia . Schizophrenia Research . 154 . 1–3 . 1–13 . Apr 2014 . 24560881 . 10.1016/j.schres.2014.01.028 . 4151500.
  11. Palmieri D, Fitzgerald D, Shreeve SM, Hua E, Bronder JL, Weil RJ, Davis S, Stark AM, Merino MJ, Kurek R, Mehdorn HM, Davis G, Steinberg SM, Meltzer PS, Aldape K, Steeg PS . Analyses of resected human brain metastases of breast cancer reveal the association between up-regulation of hexokinase 2 and poor prognosis . Molecular Cancer Research . 7 . 9 . 1438–45 . Sep 2009 . 19723875 . 10.1158/1541-7786.MCR-09-0234 . 2746883.
  12. Reid. S. Masters. C. On the developmental properties and tissue interactions of hexokinase.. Mechanisms of Ageing and Development. 1985. 31. 2. 197–212. 4058069. 10.1016/s0047-6374(85)80030-0. 40877603.
  13. Wyatt. E. Wu. R. Rabeh. W. Park. HW. Ghanefar. M. Ardehali. H. Regulation and cytoprotective role of hexokinase III.. PLOS ONE. 3 November 2010. 5. 11. e13823. 21072205. 10.1371/journal.pone.0013823. 2972215. 2010PLoSO...513823W. free.
  14. Peng Q, Zhou J, Zhou Q, Pan F, Zhong D, Liang H . Silencing hexokinase II gene sensitizes human colon cancer cells to 5-fluorouracil . Hepato-Gastroenterology . 56 . 90 . 355–60 . 2009 . 19579598 .

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Hexokinase II".

Except where otherwise indicated, Everything.Explained.Today is © Copyright 2009-2025, A B Cryer, All Rights Reserved. Cookie policy.