Fluoromethylated derivatives of carnitine biosynthesis intermediates – synthesis and applications †

A convenient method for the synthesis of fluoromethylated carnitine biosynthesis intermediates, i

Carnitine, an essential metabolite in humans and other eukaryotes, is vital for the transport of long chain fatty acids into mitochondria. 13][4] The first and last steps in the pathway are catalysed by trimethyllysine hydroxylase (TMLH) and g-butyrobetaine hydroxylase (BBOX), both of which belong to the 2-oxoglutarate (2OG) dependent oxygenase superfamily.TMLH and BBOX catalyse the hydroxylation of N e -trimethyllysine (TML, (1)) and g-butyrobetaine (GBB, (3)) respectively (Scheme 1A). 5,6The inhibition of human carnitine biosynthesis reduces fatty acid metabolism and has been targeted for the treatment of cardiovascular diseases. 7,8With respect to efforts aimed at understanding biological roles of 2OG dependent oxygenases in carnitine metabolism, 9,10 we are interested in developing reagents that enable assays for carnitine biosynthesis enzyme activities, both in vitro 11 and in more biologically representative systems.Given that the monofluoromethyl group is similar in size to the methyl group, we envisioned fluoromethylated GBB (9) and TML (11) analogues as potentially useful tool compounds for monitoring carnitine biosynthesis.
Organofluorine compounds have substantial applications in chemistry and chemical biology; their applications include the modification of physicochemical and conformational properties of small molecules, and use as tracers in radiomedicine 12 or labels in NMR studies. 13,14 19F NMR is emerging as a valuable tool for studying biochemical processes in vitro and in vivo. 15The principle advantage of 19 F NMR is that the absence of endogenous fluorinated species in most living organisms eliminates the problem of background interference and signal overlap.However, the use of 19 F NMR is often limited by the availability of appropriately labeled fluorinated compounds.
Various approaches for the incorporation of fluorine into small molecules are available, but reagents for electrophilic monofluoromethylation are limited. 16Prakash et al. reported an air and moisture stable electrophilic fluoromethylation reagent (7) that reacts under mild conditions 17 with various nucleophiles, including amines. 17,18The reported preparation of ( 7) required This journal is © The Royal Society of Chemistry 2014 the use of liquefied CH 2 FCl, which can be inconvenient.We therefore employed a route where chloromethylphenyl sulphide (5) was converted to the corresponding fluoride by reaction with caesium fluoride 19 and then directly oxidised with aqueous N-bromosuccinimide to yield fluoromethylsulphinyl benzene (6) -a known intermediate in the synthesis of the fluoromethylating reagent (7) (Scheme 1B).We then used (7) to efficiently prepare N-CH 2 F modified derivatives of GBB (3) and TML (1) in 2 or 3 steps, respectively, starting from appropriately protected N,N-dimethylated precursors (Scheme 1C).
The fluoromethylated GBB analogue (GBBNF, ( 9)) was evaluated in reaction with the purified recombinant human BBOX (hBBOX) in vitro.GBBNF ( 9) was found to be a hBBOX substrate as demonstrated by 1 H NMR analyses (Fig. S1, ESI †) undergoing hydroxylation at the C3 position to give a fluoromethylated carnitine analogue (CARNF) (14) (Fig. 1C; for NMR assignment of the product see Fig. S2-S4, ESI †), in an analogous manner to hBBOX catalysed GBB hydroxylation (Fig. 1A).We have reported the synthesis of another fluorinated analogue of GBB -(3S)-fluoro-GBB (GBBF, ( 12)), C-3 hydroxylation of which leads to fluoride release concomitant with ketone ( 13) formation (Fig. 1B). 11In NMR assays we did not observe fluoride release in reaction of GBBNF (9) with hBBOX, indicating that the fluoromethylated quaternary ammonium group is stable under the assay conditions.Comparison of the initial rates of hydroxylation of GBB (3), GBBNF (9) and GBBF ( 12) by hBBOX revealed that GBBNF ( 9) is a better substrate than GBBF (12) (Table 1, Fig. 1).The initial hydroxylation rate of GBBNF ( 9) is B65% of the initial hydroxylation rate of GBB (3), while GBBF ( 12) is hydroxylated at B20% of the initial rate of GBB (3).The K M and k cat values also reveal that the properties of GBBNF (9) as a substrate are closer to those of GBB (3) than GBBF (12) (Table 1).Some 2OG dependent oxygenases catalyse turnover of 2OG independent of substrate transformation (uncoupled 2OG turnover) 5 which can manifest with a poor substrate. 20We examined levels of uncoupled turnover when GBB (3) and its fluorinated analogues were used, by comparing rates of succinate formation to that of hydroxylation.The results showed GBBNF (9) to be similar to GBB (3) (ratio of succinate formation to hydroxylation 1.1 for GBB vs. 1.3 for GBBNF), while in the case of GBBF (12), the ratio was B2 : 1 (Table 1 and Fig. S5,  ESI †).Note that, as for GBB (3), GBBF (12) displays substantial substrate inhibition (apparently K i values in micromolar rangesee Table 1).Interestingly, the extent of substrate inhibition by GBBNF ( 9) was much less than for GBB (3) or GBBF (12) (Fig. S6,  ESI †).The mechanism of substrate inhibition of hBBOX is unknown, but is of interest as it may be involved in regulating carnitine biosynthesis in cells.
hBBOX catalysed GBBNF (9) hydroxylation can be followed by 19 F NMR, because the fluorine shift of the product is distinctively different from a shift of the substrate (Fig. 2A).In these compounds the 19 F resonance appears with a 1 : 1 : 1 triplet fine structure, not as a singlet.This structure arises from coupling of the fluorine to the adjacent quadrupolar 14 N nucleus (I = 1, 99.6% abundance) and is Fig. 1 Reactions catalysed by BBOX.GBBNF is a BBOX substrate and undergoes hydroxylation in a position analogous to GBB hydroxylation.Time dependent product formation reveals that GBBNF is a better substrate than GBBF.apparent because the highly symmetrical tetrahedral environment of the 14 N centre suppresses rapid quadrupolar relaxation that, in less symmetrical environments, leads to loss of coupling fine structure. 19F NMR can also be employed for IC 50 measurements (Fig. 2B).We investigated hBBOX inhibition by Mildronate, 7 which is an inhibitor and a competitive substrate for hBBOX. 9,10The obtained IC 50 value (82 mM) is similar to that obtained by 1 H NMR (34 mM) and fluoride release (65 mM) assays. 11The differences likely reflect the different assay conditions used.Thus, 19 F NMR assay employing GBBNF (9) as a substrate is useful for in vitro activity studies.An advantage of the GBBNF (9) based system is its ability to monitor specific hBBOX turnover without the interference of any other non-fluorinated components, making it suitable for biologically relevant assay conditions.
To test the turnover of fluorinated analogues in cells we used E. coli BL21 cells producing a prokaryotic BBOX homologue from Pseudomonas sp.AK1 (psBBOX).We observed that GBBNF (9) is converted to CARNF (14) in crude cell lysates, provided that 2OG was added to the reaction mixture, and that the turnover level is dependent on 2OG concentration (Fig. S7, ESI †).The extent of GBBNF (9) turnover is dependent on the amount of psBBOX present in the extracts (Fig. 2C and Fig. S8, ESI †).Thus, 19 F NMR can be used to estimate psBBOX activities in cell lysates.
In addition to the use as a label for 19 F NMR studies, fluorine is a convenient marker for small molecules in MS based studies.We therefore investigated the metabolism of TMLNF (11) in human embrionic kidney cells (HEK 293T cells) using LC-MS.HEK 293T cells were grown either with or without TML (1) or TMLNF (11) added to the growth media.Cells were harvested, lysed and analysed for the carnitine related metabolites (Fig. 3), using appropriate standards (Fig. S10, ESI †).In none of the samples could TML (1) or TMLNF (11) be detected.In the sample treated with TML (1), elevated levels of GBB (3) were observed, indicating that TML (1) penetrates cell membranes and is converted to GBB (3).Cells treated with TMLNF (11) contained lower amounts of GBB (3) than controls and substantial levels of GBBNF (9), which can only be formed from TMLNF (11), demonstrating that TMLNF (11) is carried through the first enzyme catalysed step of carnitine biosynthesis.All of the samples contained similar levels of carnitine (within error), but no CARNF (14) was observed in the TMLNF (11)   treated sample; this result may reflect the differences in affinities of GBB (3) and GBBNF (11) to hBBOX, as observed by in vitro kinetic data (Table 1).
In conclusion we have described an efficient procedure for the synthesis of the electrophilic monofluoromethylation reagent 17  (7) that enables convenient preparation of fluoromethylated quaternary ammonium derivatives, e.g.trimethyllysine and carnitine related compounds.The utility of these compounds in enzymatic assays was demonstrated employing 19 F NMR with recombinant hBBOX and crude cell lysates.LC-MS studies enabled tracking of fluorinated intermediates in human cells.Quaternary ammonium derivatives have widespread pharmaceutical and industrial applications e.g. as antimicrobial agents 21 or phase transfer catalysts in organic chemistry. 22They are also a ubiquitous class of metabolites, present in all living organisms. 23In humans and animals N-methylated lysine, arginine and nucleic acid compounds play crucial roles in epigenetic regulation.We hope that the development of appropriate fluorinated small molecules will enable work aimed at understanding the role of methylation in epigenetics.

FluoromethylatedF
derivatives of carnitine biosynthesis intermediates -synthesis and applications † Anna M. Rydzik, a Ivanhoe K. H. Leung, a Armin Thalhammer, a Grazyna T. Kochan, ‡ b Timothy D. W. Claridge a and Christopher J. Schofield* a A convenient method for the synthesis of fluoromethylated carnitine biosynthesis intermediates, i.e. fluorinated derivatives of c-butyrobetaine and trimethyllysine, is described.The fluoromethylated probes were useful in both in vitro and cell based assays employing 19 NMR and LC-MS analyses.

Fig. 2
Fig.2Applications of GBBNF(9).A -conversion of GBBNF to CARNF by psBBOX can be followed by19 F NMR. B -19 F NMR based assay enables determination of dose-response curves for potential inhibitors, exemplified with the hBBOX inhibitor Mildronate.C -SDS-PAGE gel shows lysate samples from cells harvested at various times after IPTG induction (lanes 4-8).Molecular weight marker (lane 1), BBOX sample (lane 2) and uninduced cells harvested after 24 h (lane 3) are shown.BBOX activity in cell lysates can be quantified by19 F NMR.

Table 1
Kinetic properties of fluorinated GBB analogues