In the present study we characterize the properties of the potent MCT1 (monocarboxylate transporter 1) inhibitor AR-C155858. Inhibitor titrations of L-lactate transport by MCT1 in rat erythrocytes were used to determine the Ki value and number of AR-C155858-binding sites (Et) on MCT1 and the turnover number of the transporter (kcat). Derived values were 2.3±1.4 nM, 1.29±0.09 nmol per ml of packed cells and 12.2±1.1 s−1 respectively. When expressed in Xenopus laevis oocytes, MCT1 and MCT2 were potently inhibited by AR-C155858, whereas MCT4 was not. Inhibition of MCT1 was shown to be time-dependent, and the compound was also active when microinjected, suggesting that AR-C155858 probably enters the cell before binding to an intracellular site on MCT1. Measurement of the inhibitor sensitivity of several chimaeric transporters combining different domains of MCT1 and MCT4 revealed that the binding site for AR-C155858 is contained within the C-terminal half of MCT1, and involves TM (transmembrane) domains 7–10. This is consistent with previous data identifying Phe360 (in TM10) and Asp302 plus Arg306 (TM8) as key residues in substrate binding and translocation by MCT1. Measurement of the Km values of the chimaeras for L-lactate and pyruvate demonstrate that both the C- and N-terminal halves of the molecule influence transport kinetics consistent with our proposed molecular model of MCT1 and its translocation mechanism that requires Lys38 in TM1 in addition to Asp302 and Arg306 in TM8 [Wilson, Meredith, Bunnun, Sessions and Halestrap (2009) J. Biol. Chem. 284, 20011–20021].
There are 14 members of the MCT (monocarboxylate transporter) family (SLC16) encoded by the human and mouse genomes . Of these only MCT1, MCT2, MCT3 and MCT4 have been demonstrated to catalyse the bidirectional proton-linked transport of short-chain monocarboxylates such as L-lactate and pyruvate across the plasma membrane of mammalian cells [2–6]. MCT1 is expressed in most tissues and facilitates lactic acid uptake for oxidation in heart and red skeletal muscle, and for gluconeogenesis in the liver and kidney of some species [7–11]. MCT1 is also used for lactic acid efflux by some cells that are exclusively glycolytic, such as erythrocytes, and by all cells under hypoxic conditions [1,10,12]. MCT2 is a higher-affinity transporter  whose expression is more restricted and highly species-dependent . In some species it is the dominant MCT isoform in the kidney and liver where it facilitates lactic acid uptake for gluconeogenesis [9,13]. It is also expressed in neurons, especially at the post-synaptic density, and has been proposed to provide the uptake pathway for the oxidation of lactate produced by the more glycolytic astrocytes [14,15]. MCT3 expression is confined to the basal membrane of the retinal pigment epithelium and choroid plexus epithelia [16,17], but detailed information on its substrate and inhibitor specificity is lacking . MCT4 is a lower-affinity transporter [5,6] and is primarily expressed in highly glycolytic cells, such as white muscle fibres, where it is used to facilitate lactic acid efflux from the tissue [18,19]. Most cells can up-regulate MCT4 expression under hypoxic conditions when glycolytic flux is enhanced and this is mediated through transcriptional control by HIF-1α (hypoxia-inducible factor 1α) .
In view of the importance of plasma membrane lactic acid transport in metabolism, it would be desirable to have a specific inhibitor of each isoform that could probe their individual metabolic roles. A range of inhibitors of MCTs have been described, including the α-cyanocinnamate derivatives, stilbene disulfonates such as DIDS (di-isothiocyanostilbene disulfonate), phloretin, bioflavenoids such as quercetin and organomercurial reagents such as p-chlomercuribenzene sulfonate (see [1,21,22]). However, none of these is specific for inhibition of MCTs and thus they cannot be used with confidence in metabolic studies. This reservation applies particularly to α-cyano-4-hydroxycinnamate that some workers have used on the assumption that it is a specific MCT inhibitor (for example see [23–25]). However, this agent is at least two orders of magnitude more potent at inhibiting the mitochondrial pyruvate carrier than MCT1 [26–29]. Previously, a new class of specific and extremely high-affinity inhibitors of MCT1 have been discovered by AstraZeneca [30–32]. These compounds were originally identified as potent inhibitors of T-lymphocyte proliferation that act as immunosuppressants and were subsequently shown to bind to MCT1 and MCT2, but not MCT4 . Since T-lymphocyte activation and proliferation is accompanied by a large (up to 14-fold) stimulation of glycolysis, it would appear that inhibiting MCT1 and so preventing the efflux of the resulting lactic acid is responsible for the compounds' immunosuppressive activity .
In the present study we seek to characterize the mode of action of one of these potent MCT1 inhibitors, AR-C155858. We have studied the concentration dependency of AR-C155858 inhibition of lactate transport into rat erythrocytes mediated by endogenous MCT1, as well as its effects on the activity of MCT1, MCT2 and MCT4 expressed in Xenopus laevis oocytes. We show that AR-C155858 inhibits MCT1 and MCT2 with similar potency, but is inactive against MCT4, and that inhibition is exerted by the drug binding to a site on MCT1 accessible from the cytosol. The use of MCT1/MCT4 chimaeric transporters reveals that this binding site is contained within TM (transmembrane) helices 7–10 of MCT1. In rat erythrocytes a detailed analysis of the inhibition of lactate transport by AR-C155858 has enabled us to determine the turnover number (kcat) of MCT1 (12.2 s−1 at 6 °C) and the Ki value for AR-C155858 (2.3 nM).
X. laevis toads were obtained from Xenopus Express and oocytes were harvested as described previously . All reagents were obtained from Sigma unless otherwise stated. Polyclonal antibodies against the C-terminal 16 amino acids of rat MCT1, MCT2 and MCT4, and against a 17 amino acid sequence between TM7 and TM8 of MCT1 were raised in rabbits as described previously [9,18,34]. Anti-rabbit secondary antibodies for immunofluorescence microsocopy were from Jackson ImmunoResearch. L-[14C]Lactate was obtained from GE Healthcare and [14C]pyruvate was from PerkinElmer. AR-C155858 (whose structure is shown as an inset to Figure 1) was obtained from AstraZeneca and made up as a 10 mM stock in DMSO.
L-lactate uptake into rat erythrocytes by AR-C155858
Generation of MCT chimaeras of rat MCT1 and MCT4 was performed by PCR using pfu Taq polymerase (Roche). The two appropriate segments of MCT1 and MCT4 were produced with a region of overlapping sequence that was used to splice the two together to produce the desired chimaera. For the MCT1/4 and MCT4/1 chimaeras the switch occurs at the end of the loop between TMs 6 and 7 which contains the conserved sequence LDLS. For the MCT1/4TM11 and MCT4/1TM11 chimaera the switch occurs at the beginning of TM11 containing the conserved sequence FSSA. However, for the C-terminal chimaeras MCT1/4c and MCT4/1c, where the switch occurs at the beginning of the C-terminus, there is no conserved sequence and thus a region of complimentarity was manufactured using modified primers . A C-terminal truncation of MCT1 was produced using PCR to amplify the MCT1 sequence minus the C-terminus, and this was subsequently inserted into the oocyte expression vector pGHJ with the addition of a stop codon in the vector downstream of the MCT sequence. Sequences for all primers used are given in Supplementary Table S1 (at http://www.BiochemJ.org/bj/425/bj4250523add.htm) and were designed to be between 15 and 30 bases in length. Typically, for an MCT fragment, thermocycling was performed using the following parameters: 30 s at 95 °C, 30 s at 55 °C and a 1.5 min extension at 72 °C for 30 cycles. Subsequently, appropriate fragments of MCT1 and MCT4 with complimentary sequence in the cross-over region were combined using PCR with primers to the 5′- and 3′-UTR (untranslated region) of MCT1 and MCT4. Here, thermocycling was performed using the following parameters: 30 s at 95 °C, 30 s at 55 °C and a 1 min extension at 72 °C for 10 cycles followed by 30 s at 95 °C, 30 s at 50 °C and a 1 min extension at 72 °C for 25 cycles. The MCT chimaeras were subsequently ligated into the pGHJ oocyte expression vector. For the MCT1/4 and MCT4/1 C-terminal chimaeras, the C-terminal regions were brought into the correct reading frame by a single base deletion and addition respectively using site-directed mutagenesis with the QuikChange® kit (Stratagene) as described previously . Confirmation that chimaera constructs had been correctly engineered was provided by sequencing (The Sequencing Service, University of Dundee, Dundee, U.K.).
Measurement of MCT1 activity in rat erythrocytes
L-Lactate transport into rat erythrocytes was measured by monitoring the change in extracellular pH with a pH-sensitive electrode as described previously [37,38]. The cells were used at 3.5% or 7% haematocrit in lightly buffered saline medium supplemented with 5 μM DIDS and 100 μM acetazolamide to prevent bicarbonate/CO2-mediated proton movements [37,38]. The erythrocytes were pre-incubated for 1 h at room temperature (22–25 °C) with or without AR-C155858 at the required concentration prior to assaying lactate transport. This was performed at 6 °C with substrate uptake initiated by addition of 10 mM L-lactate. Initial rates of transport were calculated by first-order regression analysis of the time course of pH change and converted into nmol of H+ per min by determining the pH change induced by small additions of standardized NaOH.
Measurement of MCT transport activity in
cRNA was prepared by in vitro transcription from the appropriate linearized pGHJ plasmid (mMessage mMachine, Ambion) and injected into X. laevis oocytes as described previously . For most assays 20 ng of cRNA was injected, but for [14C] kinetic assays, injection quantity was adjusted to ensure that uptake was linear with time. Further details can be found in Supplementary Table S2 (at http://www.BiochemJ.org/bj/425/bj4250523add.htm). Controls received the equivalent volume (9.2 nl) of water. Oocytes were then cultured in OR3 medium for 72 h with fresh medium each day. Rates of L-lactate transport by wild-type or chimaeric MCTs were determined as described previously, either by following the change in intracellular pH using the ratiometric pH-sensitive fluorescent dye BCECF [2′-7′-bis(carboxyethyl)-5(6)-carboxyfluorescein] [6,38] or by measuring uptake of [14C] substrate (L-lactate or pyruvate) . For measurement of AR-C155858 sensitivity, ten oocytes were placed in a six-well plate containing 5 ml of uptake buffer [75 mM NaCl, 2 mM KCl, 0.82 mM MgCl2, 1 mM CaCl2 and 20 mM Mes (pH 6.0)] and allowed to pre-incubate for the required time (usually 45 min) with or without AR-C155858 as required. Five oocytes were removed and placed into 50 μl of uptake buffer containing L-[14C]lactate (0.5 mM, 7.4 MBq/ml) with or without AR-C155858 at the required concentration. Incubation at room temperature was continued for the period over which uptake was linear with time; this varied with the construct employed, as detailed in Supplementary Table S2. The oocytes were then rapidly washed five times with ice-cold uptake buffer and, after the final wash, each egg was transferred into a scintillation vial and homogenized in 100 μl of 2% (w/v) SDS by vigorous vortex-mixing. Scintillation fluid (10 ml of Emulsifier-Safe, PerkinElmer) was then added and [14C] assayed by scintillation counting.
For the determination of Km values for pyruvate and L-lactate, oocytes were equilibrated in incubation buffer [75 mM NaCl, 2 mM KCl, 0.82 mM MgCl2, 1 mM CaCl2 and 20 mM Tris/Hepes (pH 7.4)] for 5 min and then four oocytes incubated with 40 μl of uptake buffer containing [14C]-labelled L-lactate or pyruvate (7.4 MBq/ml) at a final concentration of 0.2, 0.5, 1, 2, 5, 20, 50 and 75 mM. Incubation was continued for the period over which uptake was linear with time (detailed in Supplementary Table S2), following which oocytes were washed and prepared for scintillation counting as above. Net MCT1-mediated uptake of L-lactate was determined by subtracting the uptake by water-injected oocytes determined at the same time.
Ki of AR-C155858 for MCT1 in rat erythrocytes
Rat erythrocytes support very rapid lactate transport that is mediated by three mechanisms. The majority is via MCT1, but a small proportion may occur via the anion exchanger AE1 and by free diffusion of the undissociated lactic acid [26,40]. Transport mediated by AE1 can be blocked by 5 μM DIDS, a concentration that has a minimal effect on MCT1 [37,38]. Using a pH electrode to determine the extracellular increase in pH that accompanies the proton-linked transport of 10 mM L-lactate into erythrocytes at 6 °C we have investigated the inhibition of MCT1 by AR-C155858. It was first established that inhibition by low (nanomolar) concentrations of AR-C155858 reached equilibrium within 30–45 min incubation at room temperature (results not shown). Thus for detailed inhibitor titrations with increasing concentrations of AR-C155858 we used 60 min incubation of erythrocytes at both 3.5 and 7% haematocrit. After incubation with inhibitor at room temperature, cell suspensions were cooled to 6 °C before measurement of L-lactate transport and determination of initial rates. In Figure 1 we show that the concentration-dependence of inhibition is almost linear up to 80% inhibition, as predicted for a very tight-binding inhibitor whose concentration is less than the concentration of the target protein (MCT1). By performing parallel experiments at two cell densities (3.5% and 7% haematocrit) the data can be fitted by non-linear regression analysis to the equation for a tight-binding non-competitive inhibitor using the total inhibitor concentration and the haematocrit as the two x-variables [41,42]. This allowed us to determine values (±S.E. for the fit shown) for the Ki (2.3±1.4 nM), the number of binding sites (Et) for AR-C155858 inhibition (1.29±0.09 nmol per ml of packed cells) and the turnover number (kcat) of MCT1 in rat erythrocytes (12.2±1.1 s−1).
Time- and concentration-dependence of MCT inhibition by AR-C155858 in
In order to perform accurate comparisons of the affinity of the different MCT isoforms towards AR-C155858 we expressed MCT1, MCT2 and MCT4 in X. laevis oocytes. It was first necessary to ensure that the time of incubation of oocytes with inhibitor was sufficient to allow compound binding to the MCT to reach equilibrium. In Figure 2 the rate of [14C]lactate uptake into MCT1-expressing oocytes was determined after incubation with 0.1 μM AR-C155858 for 15, 30, 45 and 60 min. For each time point, mean data (±S.E.M) for ten separate oocytes are presented. The data show that, as with the erythrocytes, 45 min incubation with inhibitor was sufficient to give maximal inhibition. As might be predicted, with 1 μM AR-C155858 inhibition occurred much more quickly and was almost maximal at 5 min. This was confirmed by BCECF assay of transport as shown in the inset to Figure 2. From these data we chose to use a 45 min incubation time for comparing the relative potency of AR-C155858 as an inhibitor of MCT1, MCT2 and MCT4. In Figure 3 we show that the concentration-dependence of MCT1 follows a linear trend up to 30 nM (70% inhibition) and then curves off towards 100% inhibition at 100 nM. Again, this behaviour is that predicted for a very high-affinity inhibitor and thus consistent with the Ki for AR-C155858 of 2.3 nM determined using rat erythrocytes. By contrast, oocytes expressing MCT4 at levels supporting similar rates of lactate transport revealed no significant inhibition by 1 μM AR-C155858, and even at 10 μM AR-C155858 inhibition was only approx. 20%. In oocytes expressing MCT2 the initial rate of transport was less than for MCT1 and MCT4, consistent with the poorer expression of MCT2 at the plasma membrane as reported previously . This is a consequence of MCT2 binding less well to the endogenous basigin expressed by Xenopus oocytes than does MCT1 and MCT4 [38,43]. Nevertheless, it is clear that MCT2 is potently inhibited by AR-C155858, and the 70% inhibition seen at 10 nM is followed by a gradually increasing inhibition which can only be explained by a Ki value of significantly less than 10 nM.
MCT1 expressed in
Xenopus oocytes is inhibited by AR-C155858 in a time- and concentration-dependent manner
When expressed in
Xenopus oocytes, MCT1 and MCT2, but not MCT4, are sensitive to inhibition by AR-C155858
Extrapolation of the linear portion of the plot shown for MCT1 inhibition to zero carrier-mediated rate (i.e. water-injected rate) provided an estimated concentration of MCT1 in the incubation of 40 nM. Each egg was incubated in 10 μl so this represents 0.4 pmol of MCT1 per egg. The rate of L-lactate uptake was approx. 95 pmol/egg per min which gives a turnover number of 4 s−1 for MCT1 in oocytes at 22 °C with 0.5 mM L-lactate. Since the initial slope of the inhibitor plot for MCT2 cannot be accurately determined, it is not possible to determine an accurate turnover number for this isoform. Nevertheless, linear extrapolation of the plot would give a maximal value for the concentration of MCT2 to be approx. 15 nM, corresponding to a maximal expression of MCT2 of 0.15 pmol per egg. This would yield a minimum estimate of the turnover number for MCT2 in oocytes at 22 °C with 0.5 mM L-lactate of 5 s−1, which is similar to MCT1.
AR-C155858 probably binds to MCT1 from the cytosolic side
The slow time-dependence of inhibition by AR-C155858 could reflect slow binding to a site on the external surface or perhaps, more likely, a slow permeation of the inhibitor into the cell where it binds to an internal site on MCT1. In order to discriminate between the two possibilities we microinjected 9.2 nl of 1 mM AR-C155858 into oocytes, corresponding to a total internal concentration of approx. 23 μM (assuming an internal volume of 0.4 μl per egg  and ignoring binding to intracellular components). Each oocyte (20 in total) was immediately transferred into 5 ml of pH 6 transport buffer and then left for 5 min prior to washing once and determining the rate of L-[14C]lactate uptake. As a control, the same quantity of inhibitor (184 nl corresponding to 20 oocytes worth of inhibitor) was added to 5 ml of buffer (36.8 nM final) prior to addition of 20 oocytes and 5 min incubation. These oocytes were subsequently washed and transport determined as for AR-C155858-injected oocytes. As an additional control, some oocytes were injected with 9.2 nl of DMSO. The results in Figure 4 show that the rate of L-lactate uptake was approx. 50% inhibited in the AR-C155858-injected oocytes, whereas the same quantity of inhibitor added outside was without effect. It might also be argued that the slow time course of inhibition could reflect internalization of MCT1. However, the immunofluorescence results in Figure 4 confirm that the expression of MCT1 at the plasma membrane was unchanged in oocytes incubated with 1 μM AR-C155858 for 1 h to give full inhibition of transport.
Microinjection of AR-C155858 inhibits MCT1 expressed in
AR-C155858 inhibition involves TM helices 7–10 in the C-terminal half of MCT1
Since MCT1 is inhibited by AR-C155858, whereas MCT4 is not, we made MCT1/4 chimaeras to establish the region on MCT1 to which the inhibitor binds. The structures of these MCT1/4 chimaeras are shown schematically in (A) of each relevant Figure. We first created chimaeras in which the N-terminal half and large intracellular loop were of MCT1 and the C-terminal half was from MCT4. This chimaera (MCT1/4) was expressed at the plasma membrane of oocytes and transported L-lactate, albeit at a greatly reduced rate (Figure 5B). However, like MCT4, it was insensitive to inhibition by AR-C155858 (Figure 5C). We also made the reverse chimaera MCT4/1. It too was expressed at the plasma membrane, although there appeared to be a significant amount of the chimaera that was in a vesicular compartment and not at the plasma membrane (Figure 5B). Nevertheless, this MCT4/1 chimaera showed a sensitivity to AR-C155858 similar to MCT1 (Figure 5C). Thus our results imply that the binding site of MCT1 for AR-C155858 is contained within the C-terminal half of the molecule, beyond the intracellular loop between TMs 6 and 7.
The binding site of MCT1 for AR-C155858 resides within the C-terminal half of the transporter
In order to define the binding site of the inhibitor more precisely we created additional chimaeras. We first made chimaeras in which either the C-terminal tail of MCT1 was removed or swapped for that of MCT4 as shown schematically in Figure 6(A). Both the MCT1trnc and MCT1/4c were expressed at the plasma membrane of oocytes, although a significant amount of MCT1trnc remained intracellular. Nevertheless, this chimaera still transported lactate with rates similar to that seen with normal MCT1 and MCT4. Although we did not perform detailed inhibitor titrations we showed that both the MCT1/4c chimaera and MCT1trnc were strongly inhibited by 0.1 μM AR-C155858, like MCT1 itself. These results imply that the binding site for AR-C155858 does not require the C-terminal tail of MCT1. In order to establish which of the C-terminal TM helices might be important for inhibitor binding we compared the C-terminal TM sequences of MCT1, MCT2 and MCT4 and found that it was within TM11 that MCT4 (inhibitor-insensitive) exhibited the greatest difference to MCT1 and MCT2 (inhibitor-sensitive). Thus we made chimaeras in which the switch between MCT1 and MCT4 was performed at the start of TM11. Unfortunately, as shown in the inset to Figure 7(B), the MCT1/4TM11 chimaera was not expressed properly at the plasma membrane and no enhancement of L-lactate transport over water-injected eggs was detected. However, the MCT4/1TM11 chimaera was expressed at the plasma membrane and did transport L-lactate, albeit very slowly (Figure 7B). Subtraction of the very low background rate of lactate transport by uninjected oocytes, which was inhibited by AR-C155858, revealed that the residual lactate transport activity mediated by MCT4/1TM11 was insensitive to inhibition by AR-C155858. This suggests that the binding site for AR-C155858 does not involve TMs 11 and 12 as we had initially reasoned and must therefore involve TMs 7–10.
The C-terminus of MCT1 is not involved in AR-C155858 sensitivity
A region within TMs 7–10 of MCT1 is required for sensitivity to AR-C155858
Kinetic properties of the MCT1/4 and MCT4/1 chimaeras
The relatively low rates of transport seen with the MCT4/1 and MCT1/4 chimaeras may reflect a high Km for L-lactate and thus low rates of transport when measured at 0.5 mM L-lactate. In order to investigate this possibility, and to provide some clues as to how the two halves of the MCT might be involved in substrate binding, the Km values of the chimaeras for L-lactate and pyruvate were determined (Table 1). The MCT4/1 chimaera exhibited a Km value for L-lactate of 15–25 mM, depending on whether the BCECF or radioactive assay was used, whereas both techniques gave a Km value for pyruvate of 8–9 mM. These Km values are similar to that of MCT4 in the case of L-lactate, but intermediate between MCT1 and MCT4 for pyruvate. In the case of the MCT4/1 chimaera, Km values were too high to be determined radioactively, but using BCECF they were found to be 209±72 mM for L-lactate and 27±5 mM for pyruvate. Thus with this chimaera also, the Km for pyruvate was intermediate between MCT1 and MCT4, whereas the Km for L-lactate was much higher than that for either isoform.
|Km value (mM) using [14C] substrate||Km value (mM) using BCECF|
|MCT1||5.7±1.2 (n=16)||1.2±0.2 (n=16)||3.5*||1*|
|MCT4||12.9±2 (n=16)||103±28 (n=24)||28*||150*|
|MCT1/4||26.5±5.7 (n=16)||8.9±2 (n=16)||15.8±2.6 (n=7)||8.5±1.9 (n=9)|
|MCT4/1||−||−||209.2±71.9 (n=7)||27.3±5.2 (n=8)|
|Km value (mM) using [14C] substrate||Km value (mM) using BCECF|
|MCT1||5.7±1.2 (n=16)||1.2±0.2 (n=16)||3.5*||1*|
|MCT4||12.9±2 (n=16)||103±28 (n=24)||28*||150*|
|MCT1/4||26.5±5.7 (n=16)||8.9±2 (n=16)||15.8±2.6 (n=7)||8.5±1.9 (n=9)|
|MCT4/1||−||−||209.2±71.9 (n=7)||27.3±5.2 (n=8)|
BCECF data for MCT1 and MCT4 are taken from .
Previously, a new class of specific and extremely potent inhibitors of MCT1 have been discovered by AstraZeneca that were reported to show no binding to MCT4 and exhibit lower-affinity binding to MCT2 [30–32]. The Kd values for these inhibitors binding to endogenous MCT1 in rat and human cells was found to be in the low nanomolar region or less, as was also found for MCT1 expressed in Ins-1 cells that contain little or no endogenous MCT1 [30,31]. Similar Kd values were determined for MCT1 expressed in yeast , and the Ki value of AR-C155858 for MCT1 we have determined in rat erythrocytes of 2.3±1.4 nM is entirely consistent with the Ki of 1.2 nM for binding of AR-C155858 to human erythrocyte MCT1 derived from radioligand-binding experiments .
The turnover number for MCT1 can be calculated using AR-C155858
The inhibitor titration in rat erythrocytes has allowed us to determine the concentration of MCT1 in these cells to be 1.29±0.09 nmol per ml of packed cells. Since the number of erythrocytes in 1 ml of packed blood is known to be approx. 1010  it is possible to calculate that there are approx. 80000 molecules of MCT1 per rat erythrocyte. This value is quite similar to the value of 46000±11000 determined previously by [3H] inhibitor binding  and represents approx. 8% of the value for the anion exchanger AE1 . Using the rate of L-lactate transport and the concentration of MCT1 we calculated the turnover number (kcat) to be 12.2±1.1 s−1 at 6 °C. Since we have previously determined the temperature-dependence of MCT1 , we are able to calculate that the rate of L-lactate transport by rat erythrocytes at room temperature will be approx. 7-fold higher than at 6 °C. This would bring the predicted turnover number for MCT1 in rat erythrocytes to approx. 85 s−1 which is similar to the value of 35 s−1 determined for the glucose transporter GLUT1 in rat erythrocytes at 20 °C [46,47], but approx. 5-fold less than the kcat determined for endogenous human GLUT1 in erythrocytes or when overexpressed in Xenopus oocytes .
When expressed in Xenopus oocytes, MCT1 also showed time-dependent inhibition by AR-C155858 (Figure 2) with the extent of inhibition being linear with respect to AR-C155858 concentrations up to approx. 70% inhibition (Figure 3). This is consistent with a very low (nanomolar) Ki value determined in erythrocytes. By extrapolation of the linear portion of the inhibitor titration we were able to estimate that the amount of MCT1 expressed at the plasma membrane was approx. 0.4 pmol per oocyte. From this value and the rate of lactate transport, the turnover number of MCT1 in oocytes at 22 °C was calculated to be 4 s−1. However, this value was determined at 0.5 mM L-lactate and thus cannot be compared directly with the value of 85 s−1 calculated for rat erythrocytes at 22 °C with 10 mM L-lactate. The Km for MCT1 in erythrocytes and oocytes is approx. 3.5 mM [6,29], and thus from Michaelis–Menten kinetics the rate of transport at 10 mM L-lactate would be predicted to be 6-fold higher than at 0.5 mM. This would increase the turnover number of MCT1 in oocytes to 24 s−1, which is approx. 30% of the value determined for MCT1 in erythrocytes. However, we have shown previously that the rate of L-lactate uptake by oocytes determined radioactively underestimates the true transport rate determined with BCECF . This is because of an unstirred layer effect that slows diffusion of L-[14C]lactate taken up into the body of the oocyte. Thus overall there is reasonable agreement between the values measured in erythrocytes and oocytes.
AR-C155858 is a potent inhibitor of MCT1 and MCT2, but not MCT4
In agreement with competition-binding studies of MCTs expressed in yeast for related compounds , we have shown that AR-C155858 inhibits both MCT1 and MCT2, but not MCT4 when expressed in oocytes (Figure 3). Although we were unable to determine an accurate Ki value for inhibition of MCT2 by AR-C155858, we can conclude from the shape of the inhibitor titration that the value must be significantly less than 10 nM. In previous studies of inhibitor binding to MCT1 and MCT2 expressed in yeast, Kd values of 4.9 and 100 nM respectively were determined (P. A. Rugman, A. P. Jackson and C. M. Murray, unpublished work). For MCT1 this represents a reasonable agreement with the Ki values for endogenous MCT1 in rat and human cells derived in the present study and previously . However, this is not the case for MCT2 where the yeast binding data suggest that the affinity of MCT2 for AR-C155858 is more than an order of magnitude less than for MCT1. One explanation for this difference may be the absence of either basigin or embigin when MCTs are expressed in yeast, and this might affect inhibitor binding. In this context it may be noted that inhibition of MCT1 and MCT2 by the organomercurial reagent p-chloromercuribenzene sulfonate also depends on the associated ancillary protein . Our results would also imply that interpretation of metabolic studies in which AR-C122982 has been used to discriminate between MCT1- and MCT2-mediated lactate transport  may not be straightforward.
The binding site for AR-C155858 involves TMs 7–10 of MCT1, and probably faces the cytosol
The use of MCT1/MCT4 chimaeric transporters reveals that the binding site for AR-C155858 is contained within the C-terminal half of the transporter. Thus MCT1/4, like MCT4, was insensitive to inhibition by AR-C155858, whereas MCT4/1 was inhibitor-sensitive, like MCT1 (Figure 5). The C-terminal tail of MCT1 appears to have no major effect on the sensitivity to inhibition by AR-C155858 since potent inhibition by AR-C155858 was still observed when it was either removed or replaced with the tail of MCT4 (Figure 6). However, the chimaera containing TMs 1–10 of MCT4 and TMs 11 and 12 plus the C-terminal tail of MCT1 was insensitive to AR-C155858 (Figure 7). These results demonstrate that the binding site for AR-C155858 is contained, at least in part, within TMs 7–10 of MCT1. The slow time-dependence of inhibition by AR-C155858 (Figure 2) could be explained either by the inhibitor having to enter the cell before binding to an intracellular site on MCT1 or by internalization of MCT1 upon inhibitor binding. However, we showed that no MCT1 internalization occurred, even at full inhibition, and that the inhibitor worked well if microinjected into oocytes (Figure 4). These results imply that the binding site for AR-C15585 probably faces the cytosol, where our molecular model of MCT1 predicts TMs 7 and 10 to form part of the inward facing substrate-binding pocket [33,36]. This is also consistent with earlier observations that Phe360 in TM10 is involved in substrate binding since its mutation to cysteine allows MCT1 to accommodate the larger monocarboxylate mevalonate [7,50]. Furthermore, we have previously shown that Asp302 and Arg306 in TM8 are critical residues in the translocation cycle. However, analysis of the kinetics of MCT1/4 and MCT4/1 chimaeras suggest that substrate binding may not be exclusively located within the C-terminal half of MCT1. Thus both the C- and N-terminal halves of the MCT influence the kinetics of transport (Table 1). This is entirely consistent with our recent molecular model of MCT1 which predicts that the substrate-binding pocket and translocation channel involve helices from both the C- and N-terminal domains with critical roles for Lys38 in TM1, and Asp302 plus Arg306 in TM8 [33,36].
Matthew Ovens performed the oocyte studies, Andrew Davies the erythrocyte work and Marieangela Wilson provided molecular biological expertise especially for the creation of chimaeric transporters. Clare Murray advised on the use of AR-C155858 whereas Andrew Halestrap directed the research and wrote the manuscript with assistance from Matthew Ovens and Clare Murray.
We thank Agnieszka Bierzynska for skilled technical support.
This work was supported by The Wellcome Trust [Project Grant number 079792/z/06/]; and the Medical Research Council (Ph.D. studentship to M.J.O.).