Difference between revisions of "Monocarboxylate (Lactate) transporter"
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− | *Monocarboxylate transporter (MCT) 4 is the major monocarboxylate transporter isoform present in white skeletal muscle and is responsible for the efflux of lactic acid produced by glycolysis <ref name="manning_2000">Manning Fox JE ''et. al.'' (2000). ''Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle''. J Physiol 529(Pt2):285-293</ref>. In animals, L-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation. Therefore in this model the Km value for L-Lactate is only considered. By characterizing MCT4 expressed in Xenopus oocytes the <math>Km_{Lactate_{in}}</math> is defined as <math>28 \pm 4</math> and <math>V_{mf} = 2.5 \pm 0.2</math> <ref name="manning_2000">. | + | *Monocarboxylate transporter (MCT) 4 is the major monocarboxylate transporter isoform present in white skeletal muscle and is responsible for the efflux of lactic acid produced by glycolysis <ref name="manning_2000">Manning Fox JE ''et. al.'' (2000). ''Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle''. J Physiol 529(Pt2):285-293</ref>. In animals, L-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation. Therefore in this model the Km value for L-Lactate is only considered. By characterizing MCT4 expressed in Xenopus oocytes the <math>Km_{Lactate_{in}}</math> is defined as <math>28 \pm 4</math> and <math>V_{mf} = 2.5 \pm 0.2</math> <ref name="manning_2000"></ref>. |
Revision as of 15:56, 2 May 2014
Monocarboxylate transporters,[1] or MCTs, constitute a family of proton-linked plasma membrane transporters that carry molecules having one carboxylate group (monocarboxylates), such as lactate and pyruvate.
Contents
Chemical equation
![Lactate_{in} \rightleftharpoons Lactate_{out}](/wiki/images/math/9/4/7/9473e479aa23c3e2aa5b6b08d60ad0d7.png)
Rate equation
Reversible Michaelis-Menten rate law is used
Parameter values
Parameter | Value | Units | Organism | Remarks |
---|---|---|---|---|
![]() |
2.5 [2] | ![]() |
Human tumor cells | |
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2.4 [3] | ![]() |
Rat liver cells | |
![]() |
4.5 [3] | mM | Rat liver cell | |
![]() |
4.54 [2] | mM | Human tumor cells |
Parameters with uncertainty
- Monocarboxylate transporter (MCT) 4 is the major monocarboxylate transporter isoform present in white skeletal muscle and is responsible for the efflux of lactic acid produced by glycolysis [2]. In animals, L-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation. Therefore in this model the Km value for L-Lactate is only considered. By characterizing MCT4 expressed in Xenopus oocytes the
is defined as Failed to parse (Cannot store math image on filesystem.): 28 \pm 4 and Failed to parse (Cannot store math image on filesystem.): V_{mf} = 2.5 \pm 0.2 [2].
Parameter | Value | Units | Organism | Remarks |
---|---|---|---|---|
![]() |
Failed to parse (Cannot store math image on filesystem.): 2.5 \pm 0.2 | ![]() |
Human tumor cells | |
![]() |
2.4 [3] | ![]() |
Rat liver cells | |
![]() |
Failed to parse (Cannot store math image on filesystem.): 28 \pm 4 (6) | mM | Rat liver cell | |
![]() |
4.54 [2] | mM | Human tumor cells |
References
- ↑ Halestrap AP, Meredith D (2004). The SLC16 gene family-from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond. Pflugers Arch. 447 (5): 619–28 (doi)
- ↑ 2.0 2.1 2.2 2.3 2.4 Manning Fox JE et. al. (2000). Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle. J Physiol 529(Pt2):285-293
- ↑ 3.0 3.1 3.2 Jackson VN, Halestrap AP (1996) The kinetics, substrate, and inhibitor specificity of the monocarboxylate (lactate) transporter of rat liver cells determined using the fluorescent intracellular pH indicator, 2’,7’-bis(carboxyethyl)-5(6)-carboxyfluorescein. J Biol Chem 271:861–868