Versatile synthesis of probes for high-throughput enzyme activity screening
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Mass spectrometry based technologies are promising as generalizable high-throughput assays for enzymatic activity. In one such technology, a specialized enzyme substrate probe is presented to a biological mixture potentially exhibiting enzymatic activity, followed by an in situ enrichment step using fluorous interactions and nanostructure-initiator mass spectrometry. This technology, known as Nimzyme, shows great potential but is limited by the need to synthesize custom substrate analogs. We describe a synthetic route that simplifies the production of these probes by fashioning their perfluorinated invariant portion as an alkylating agent. This way, a wide variety of compounds can be effectively transformed into enzyme activity probes. As a proof of principle, a chloramphenicol analog synthesized according to this methodology was used to detect chloramphenicol acetyltransferase activity in cell lysate. This verifies the validity of the synthetic strategy employed and constitutes the first reported application of Nimzyme to a non-carbohydrate-active enzyme. The simplified synthetic approach presented here may help advance the application of mass spectrometry to high-throughput enzyme activity determination.
KeywordsEnzyme assays High-throughput Nimzyme Nanostructure-initiator mass spectrometry Chloramphenicol acetyltransferase
Given the biochemical and biotechnological significance of enzymes, high-throughput assays for the detection of enzymatic activity are in high demand. High-throughput enzyme activity assays are critical in the drug and biomarker discovery processes and can be a valuable tool for functional gene annotation. They figure prominently in directed evolution experiments, where libraries of enzyme variants are screened for improved substrate specificity, thermal stability, or other beneficial properties.
Nimzyme is a nanostructure-initiator mass spectrometry (NIMS)-based analytical technique that can detect enzymatic activity in complex mixtures such as crude cell lysate [1, 2, 3]. It circumvents time-intensive chromatographic separations by means of an in situ fluorous affinity purification (Fig. 1b). This, in combination with acoustic sample deposition , shows potential as a high-throughput enzyme activity assay.
Currently, two hurdles limit the applications of Nimzyme. First, the technique requires the chemical synthesis of a specialized analog for each substrate of interest . Second, all reported applications of Nimzyme thus far have been on enzymes acting on carbohydrates [1, 2, 3, 4]. Hence, the generalizability of the technique has yet to be demonstrated.
Here, we report a synthetic route towards Nimzyme probes in which the substrate moiety is introduced towards the end of the synthesis. Accordingly, the invariant portion of these compounds needs to be synthesized only once. By fashioning this fragment as an alkylating agent, a variety of synthetically and biologically significant molecules can be readily transformed into Nimzyme probes. We also show that a chloramphenicol analog synthesized according to this methodology is effective in detecting chloramphenicol acetyltransferase (CAT) activity in crude cell lysate.
General synthetic remarks and materials
Moisture-free conditions were employed only where indicated. Reagents and solvents were purchased from TCI America, ChemPep, Alfa Aesar, BDH, and Sigma-Aldrich, anhydrous whenever possible, and were used as received unless otherwise indicated. FluoroFlash fluorous solid-phase extraction cartridges were purchased from Fluorous Technologies Incorporated.
Design of alkylating agents
A generalized structure of Nimzyme-amenable substrate analogs as prepared in this manuscript is shown in Fig. 1c. A perfluoroalkanoyl moiety imparts the required fluorophilic character to allow for on-chip purification, and an arginine moiety ensures high ionization efficiency in NIMS . Avoiding reliance on the substrate moiety to impart ionizability also allows for direct comparison of NIMS peak heights to determine relative abundance of chemical species. A tri(ethylene glycol) linker was installed to improve enzyme–substrate accessibility and enhance the probe's solubility in water.
Nucleophilic substitution chemistry was chosen to couple substrates of interest to the probe's invariant portion because many biologically relevant substrates possess nucleophilic functional groups. Hence, we incorporated a p-toluenesulfonate ester (tosylate) leaving group into the invariant portion of the Nimzyme probe, resulting in alkylating agents 1 and 2 (Fig. 1d).
Synthesis of alkylating agents
A synthetic route to 1 and 2 was devised, which starts from readily available starting materials. A synthetic scheme, detailed synthetic protocols, and spectral data of all intermediates are reported in the Electronic Supplementary Material (Scheme S1 and S2 and Figs. S1–S11). Briefly, 2-(2-(2-aminoethoxy)ethoxy)ethanol—obtained by means of a Gabriel synthesis from 2-(2-(2-chloroethoxy)ethoxy)ethanol—was coupled to Fmoc-Arg(Pbf)-OH using conventional solution-phase peptide synthesis methodology. The Fmoc group was removed with diethylamine and the resulting amine was acylated with perfluorooctanoyl chloride under Schotten–Baumann conditions. The resulting alcohol was tosylated to afford 1 in 26 % yield with respect to Fmoc-Arg(Pbf)-OH (four steps). Lastly, the Pbf protecting group was removed with 90:10 TFA/MeOH to afford 2.
9—Ibuprofen Nz ester
Into a borosilicate test tube with stir bar, 5.7 mg ibuprofen sodium salt (25 μmol, 50 eq), 10 μL 50 mM Nz-OTs (2) in DMF, and 490 μL DMF were added. The mixture was stirred at 70 °C for 3 h. After cooling to room temperature (RT), 5 mL 1 M aqueous NaOH was added, the resulting solution was extracted with 3 × 5 mL chloroform, and each of the extracts was in turn washed with another 5 mL 1 M aqueous NaOH. A few crystals of NH3Cl were added to the chloroform extracts, which were filtered and evaporated in vacuo to yield a colorless residue which was taken up in MeOH 78 % yield.
Into a borosilicate test tube with stir bar, 50 μL 100 mM Nz(Pbf)-OTs (1) in DMF, 200 μL more DMF, and 53.1 mg (250 μmol, 50 eq) (1R,2R)-2-amino-1-(4-nitrophenyl)-1,3-propanediol were added. The mixture was stirred at 110 °C for 2 h, cooled to RT, and F-SPE purified. The eluent was evaporated in vacuo, redissolved in 2 mL 90:10 TFA/MeOH, and left to stir at RT for 12 h. The TFA/MeOH was evaporated under a gentle stream of nitrogen, leaving a white residue which was taken up in MeOH 45 % yield.
NIMS surface fabrication
The production of NIMS chips has been described elsewhere . Briefly, a silicon wafer is cleaned thoroughly with methanol, followed by anodic etching with 25 % hydrofluoric acid (w/v) in ethanol in a custom-made Teflon etching chamber using a current of 2.4 A for 15 min. Next, the chips are coated by adding the perfluorinated initiator liquid bis(heptadecafluoro-1,1,2,2-tetrahydrodecyl)tetramethyl-disiloxane for 20 min. Excess initiator is blown off with nitrogen.
Enzymatic activity assay
Overnight cultures of Escherichia coli DH1 harboring either pBbB8k-GFP or pBbB8k-CAT (the construction of these is described in the ESM) were diluted 1:10 in LB with 50 μg mL−1 kanamycin, and grown for 1 h at 37 °C, after which they were induced with 0.2 % (w/v) arabinose. After 2 h of growth, 0.5 mL of the culture was centrifuged at ∼12,000×g for 1 min, the pellet was resuspended in 0.25 mL aqueous 50 mM sodium phosphate (pH 7.5), and sonicated for 30 s. Acetyl-CoA was added to a final concentration of 2 mM and 11 to a final concentration of 0.5 mM. The mixture was mixed and incubated at room temperature for 5 min and subsequently quenched with an equal volume of methanol. A 0.3-μL droplet of the mixture was spotted onto a NIMS chip and the excess liquid removed 5 s later by touching it with a Kimwipe (Kimberly-Clark). The spotted area was washed with 2 × 1 μL deionized water. The NIMS chip was taped to a modified standard matrix-assisted laser desorption/ionization (MALDI) plate, which was then loaded into an Applied Biosystems 4800 MALDI time of flight (TOF)/TOF mass spectrometer. Agilent ESI-L Low Concentration Tuning Mix was spotted nearby on the NIMS chip to allow for mass calibration of the instrument. Spectra were acquired in manual mode and positive polarity.
We investigated the capability of 1 and 2 to react with a number of biologically relevant nucleophiles (Fig. 2a). It was found that 1 was able to alkylate alcohols by means of a Williamson ether synthesis, forming Nimzyme probes 3 and 4. Amines were likewise readily alkylated by 1 to form 5 and 6, provided the free base form was used. We used excess nucleophile to drive the reactions and to avoid over-alkylation of amines. The alkylated intermediates could be recovered using F-SPE, circumventing cumbersome chromatographic purifications. Subsequent deprotection of the Pbf group affords the desired Nimzyme probes in good yield. Alkylating agent 2 was found to react readily with carboxylate salts and phenolates to directly form Nimzyme probes 7–10. We were unable to find conditions under which these could be purified by F-SPE, and hence, we chose to remove excess nucleophile using basic aqueous washes.
Detection of chloramphenicol acetyltransferase activity
To verify that the substrate analogs synthesized according to the described methodology could be used to detect enzymatic activity in a Nimzyme assay, we synthesized chloramphenicol analog 11 as a probe for CAT activity (Fig. 2b, c). CAT catalyzes the transfer of an acetyl group from acetyl-CoA to O 3 of chloramphenicol . When 11 is exposed to a control E. coli cell lysate, Nimzyme reveals a clean mass peak corresponding to this substrate (Fig. 2d). When instead 11 is exposed to lysate from E. coli overexpressing CAT, the peak shifts by 42 mass units, as expected from monoacetylation (Fig. 2e). This result verifies the validity of the synthetic strategy employed and furthermore comprises the first reported application of Nimzyme to a non-carbohydrate-active enzyme.
In summary, we present the synthesis of a pair of alkylating agents and conditions under which they can be used to transform a wide range of structures into Nimzyme probes. The alkylation reactions and subsequent purifications are undemanding, such that an inexperienced chemist can perform them with minimal effort. One probe synthesized according to this methodology, a chloramphenicol analog, could serve to detect CAT activity in cell lysate, verifying the synthetic approach and broadening the scope of the Nimzyme technology. The other synthesized probes were not tested in enzymatic reactions in this work.
The strategy described here allows for the construction of libraries of Nimzyme substrates without the need to repeatedly re-synthesize the invariable portion of the probes. By streamlining access to compatible enzyme substrates, and by showing that Nimzyme can be applied to non-carbohydrate-active enzymes, we hope to have cleared two of the barriers to the widespread adoption of this technology for high-throughput enzyme characterization. Certain drawbacks remain to be solved, such as the possibility that the modifications required of substrates to be compatible with Nimzyme affect enzyme–substrate binding interactions. While this has been shown not to be the case for β-glycosidases , enzymes with sufficiently buried active sites may or may not accept the probes presented here as substrates. Work to overcome these shortcomings is currently ongoing.
This publication was made possible by grant number 1RC1GM090980-01 from the National Institutes of Health. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. This work was part of the DOE Joint BioEnergy Institute (http://www.jbei.org), supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research, through contract DE-AC02-05CH11231 between Lawrence Berkeley National Laboratory and the U.S. Department of Energy.
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