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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Anal Biochem. Author manuscript; available in PMC Apr 1, 2014.
Published in final edited form as:
PMCID: PMC3577954
NIHMSID: NIHMS425575

A Malachite Green-Based Assay to Assess Glucan Phosphatase Activity

Abstract

With the recent discovery of a unique class of dual-specificity phosphatases that dephosphorylate glucans, we report an in vitro assay tailored for the detection of phosphatase activity against phosphorylated glucans. We demonstrate that in contrast to a general phosphatase assay utilizing a synthetic substrate, only phosphatases that possess glucan phosphatase activity liberate phosphate from the phosphorylated glucan amylopectin using the described assay. This assay is simple and cost-effective, providing reproducible results that clearly establish the presence or absence of glucan phosphatase activity. The assay described will be a useful tool in characterizing emerging members of the glucan phosphatase family.

Keywords: Glucan, Phosphatase, Malachite green, Amylopectin, Glycogen, Starch

Glucan phosphatases are a unique class of recently discovered dual-specificity phosphatases (DSPs) present in the genomes of all mammals, some invertebrates, some protists, and all plants that remove phosphate from starch or glycogen [16]. DSPs are part of the larger protein tyrosine phosphatase (PTP) superfamily and include phosphatases with a heterogeneous array of substrates, including phosphoserine, threonine, and tyrosine residues of proteins as well as phosphatidylinositols, glycerophospholipids, mRNA, and glucans/carbohydrates [5,79]. As the PTPs play important roles in many cell-signaling events, the identification of physiological substrates for emerging DSPs is crucial. In vitro assays utilizing artificial substrates are useful for comparing enzyme kinetics, while biologically relevant substrates are necessary to compare activity within a phosphatase family (e.g. glucan phosphatases).

Many DSPs possess in vitro phosphatase activity towards phosphate esters of Ser, Thr, and Tyr of synthetic peptides [1012], as well as towards synthetic small molecule substrates such as para-nitrophenylphosphate (pNPP), 3-O-methylfluorescein phosphate (OMFP), fluorescein diphosphate (FDP), and 6,8-difluoro-4-methylumbellyferyl phosphate (DiFMUP) [10,12]. Hydrolysis of the aryl phosphate moiety from the small molecule pNPP converts this colorless substrate into para-nitrophenol, which reacts with a strong base to form the bright yellow phenolate ion that can be observed by reading the absorbance at 410 nm (Fig. 1A). Using a synthetic small molecule, one can determine the dephosphorylation kinetics and specificity constants/catalytic efficiencies of a phosphatase, and then compare these values to other phosphatases in the literature. This type of analysis can provide valuable insights into the substrate of the phosphatase. A prime example of this methodology was work on the tumor suppressor phosphatase and tensin homolog (PTEN). In vitro experiments using recombinant PTEN revealed it to be ~1000-fold less active against the phosphotyrosine analog para-nitrophenyl phosphate (pNPP) than typical tyrosine-specific PTPs. These results prompted the search for other substrates that ultimately led to the important discovery that PTEN is a phosphoinositide lipid phosphatase [13].

Figure 1
Experimental design of assays and phosphatases chosen for study

In addition to assays utilizing artificial substrates, there are in vitro assays that assess phosphatase activity against biologically relevant substrates [1,10,14,15]. Malachite green is a useful reagent in this regard, allowing colorimetric detection of picomolar amounts of inorganic phosphate due to the formation of a phosphomolybdate malachite green complex (Fig. 1B) [10,15,16]. In addition to the advantages of simplicity and sensitivity, malachite green assays have been utilized to detect phosphate released from an array of endogenous substrates such as proteins and lipids [10,14]. Herein, we describe a glucan phosphatase assay that utilizes malachite green in conjunction with the phosphorylated glucose polymer amylopectin. This assay effectively separates enzymes with glucan phosphatase activity from those that lack the activity.

First, we purified the following glucan phosphatases: human wild-type laforin and a catalytically inactive mutant serving as an experimental control (C266S), Arabidopsis thaliana Starch EXcess4 (SEX4), and Arabidopsis thaliana Like Sex Four2 (LSF2) as previously described [2,6]. We also purified or purchased phosphatases from a variety of different organisms and phosphatase families [1720]. We utilized the phosphoprotein phosphatase (PPP) family member Oryctolagus cuniculus protein phosphatase 1 (PP1) [5], the human aspartate-based phosphatase family member Dullard [5,21], and the Escherichia coli metallo-dependent protein phosphatase (PPM) family member alkaline phosphatase [22] (Fig 1C). We also employed enzymes from subfamilies within the PTP superfamily: classical PTPs such as human T-cell PTP (TCPTP) [5,23] and Yersinia pestis YopH [24,25], and dual-specificity phosphatases (DSPs) such as vaccinia virus VH1-related DSP (VHR) [2] and murine PTP localized to mitochondrion 1 (PTPMT1) [26] (Fig. 1C). These phosphatases have all previously been shown to possess phosphatase activity against substrates such as pNPP, phosphorylated peptides, phosphorylated glucans, or phospholipids [1,2,6,2124,26].

To ensure that each phosphatase we included in our work was active, we first performed phosphatase reactions with each using the small molecule pNPP (see Supplementary Material, Protocol #1). Aliquots of 5X assay buffer (100 mM sodium acetate, 50 mM Bis-Tris, 50 mM Tris) were prepared for each pH to be tested, and enzymes were diluted with 1X assay buffer containing 1 mM dithiothreitol (DTT) to a final enzyme concentration ranging from 50 to 1000ng/μl. Each reaction replicate (at least 3) was performed in a final volume of 50 μl, and consisted of 33 μl H2O, 10 μl 5X assay buffer at the optimal pH, 1 μl 100mM DTT, and 5 μl 0.5 M pNPP. We added 1 μl of diluted enzyme to each replicate tube, began timing the reaction, vortexed the tube, and then placed it at 37°C. We repeated this methodology every 15 seconds until enzyme was added to each replicate. After a reaction time of 10 minutes at 37°C, we added 200 μl of 0.25 N NaOH and vortexed the tubes to quench the reactions, and read the absorbance (A) of each replicate at 410 nm. We then utilized Beer’s Law (A=εlc, where the path length l = 1 cm) and the molar absorption coefficient (ε) of the phenolate ion under our reaction conditions (17,800 M−1 cm1) to determine the concentration in moles per liter (c) of phenolate ion generated per reaction and finally the activity of each enzyme, expressed as μmol phosphate released/min/μmol protein. Although it is common to report phosphatase activity in terms of total protein, when comparing phosphatases of different molecular weights one must compare moles of protein (Fig. 2A). However, we also provide our results in terms of total protein (Supp. Fig. 1A) for comparison with previously published activity data (Fig. 1C). All of the phosphatases tested exhibited activity against pNPP (Supp. Fig. 1A) that closely reflected previously published data at the optimal pH for each enzyme (Fig. 1C).

Figure 2
The pNPP and malachite green assays reveal specific glucan phosphatase activity only in glucan phosphatases

Next, we employed a malachite green assay to assess specific glucan phosphatase activity of the above enzymes at optimal pH using the phosphorylated glucan amylopectin as the substrate (see Supplementary Material, Protocol #2). First, we prepared the malachite green reagent. We began with 1 volume of 4.2% ammonium molybdate tetrahydrate in 4N HCl, added 3 volumes of 0.045% malachite green carbinol hydrochloride, stirred the solution for 30 minutes, filtered the solution with grade 5 Whatman filter paper, and then sterile-filtered the reagent. Prior to performing experiments with the reagent, a standard curve should be generated (see Supplementary Material, Protocol #2). Next, we prepared the amylopectin to be used as the phosphoglucan substrate. Amylopectin is largely water insoluble, therefore it must be solubilized via heating or ethanol. We prepared a suspension of 5 mg/mL of amylopectin in H2O, heated the suspension at 70°C for 30 minutes (the suspension will go from opaque to clear; vortexing aids solubility), and stored this solution at room temperature.

Before beginning the malachite green assay, we first added 0.01% (v/v) Tween 20 from a 10% stock to an aliquot of malachite green reagent. Tween 20 stabilizes the formation of the malachite green phosphomolybdate complex and prevents sedimentation of the complex for up to 48 hours [27]. We then prepared 5X assay buffer (100 mM sodium acetate, 50 mM Bis-Tris, 50 mM Tris) for each pH to be tested and diluted enzymes with 1X assay buffer with 1 mM dithiothreitol (DTT) added to a final enzyme concentration ranging from 50 to 1000ng/μl. Each reaction (at least 3 replicates) was then performed in a final volume of 20 μl consisting of 4 μl H2O, 4 μl 5X assay buffer at the optimal enzyme pH, 2 μl 100 mM of DTT, and 9 μl of 5 mg/mL amylopectin. We added 1 μl of diluted enzyme to each reaction tube, began timing the reaction, vortexed and then placed the tube at 37°C. This methodology was repeated every 15 seconds until enzyme was added to each replicate. The reactions were incubated at 37°C for 10 minutes before 20 μl 0.1M N-ethylmaleimide (NEM) was added to terminate all PTP reactions. NEM is a thiol-modifying reagent that irreversibly inhibits PTPs without affecting malachite green phosphomolybdate color formation [14]. For non-PTPs, addition of malachite green reagent was used to terminate the reaction [15]. Following NEM addition to the PTP reaction tubes, 80 μl of the malachite green reagent containing Tween20 was then added. After malachite green reagent was added to every reaction tube, the tubes were vortexed and placed at room temperature. All reactions were incubated for 40 minutes before measuring the absorbance at 620 nm [27] and calculating the pmoles of phosphate released/min/nmol protein using the standard curve.

Using the above methodology, we found that only wild-type laforin, SEX4, and LSF2 exhibited glucan phosphatase activity, while all other phosphatases that we tested possessed very little to no activity (Fig. 2B and Supp. Fig. 1B). To assess the relative activity of the phosphatases tested towards amylopectin, we compared phosphate liberation from amylopectin to pNPP activity and found that only the glucan phosphatases were effective at dephosphorylating amylopectin, with laforin being the most efficient (Fig. 2B and Supp. Fig. 1B, numbers above bars). Thus, only the glucan phosphatases possess the ability to release phosphate from amylopectin. The phosphatase assay described in this work is a simple method to characterize additional emerging members of the unique and growing family of glucan phosphatases, as has been done with the recently characterized glucan phosphatase LSF2.

Supplementary Material

01

Supplementary Figure 1pNPP and malachite green assay results reported using total protein:

A. pNPP activity. The activity of each phosphatase utilized in our study against the synthetic substrate pNPP in μmol phosphate released per minute per mg protein.

B. Glucan phosphatase activity. The specific activity of the same phosphatases against phosphorylated amylopectin in pmol phosphate released per minute per μg protein.

Acknowledgments

This work was supported by National Institutes of Health Grants R00NS061803, P20RR020171, and R01NS070899 and University of Kentucky College of Medicine startup funds to M.S.G. This publication was also supported by grant number TL1 RR033172 from the National Center for Research Resources (NCRR), funded by the Office of the Director, National Institutes of Health (NIH) and supported by the NIH Roadmap for Medical Research. The content is solely the responsibility of the authors and does not necessarily represent the official views of NCRR and NIH. We thank members from the Gentry lab and Dixon lab at UCSD, including Dr. Ji Zhang, who supplied several enzymes used in this work in addition to providing helpful information in regards to their use.

Abbreviations used

DSP
dual-specificity phosphatase
DiFMUP
6,8-difluoro-4-methylumbellyferyl phosphate
DTT
dithiothreitol
FDP
fluorescein diphosphate
LSF2
Like SEX4 2
OMFP
3-O-methylfluorescein phosphate
NEM
N-ethylmaleimide
pNPP
para-nitrophenylphosphate
PP1
protein phosphatase 1
PPM
metallo-dependent protein phosphatase
PPP
prosphoprotein phosphatase
PTP
protein tyrosine phosphatase
PTPMT1
protein tyrosine phosphatase localized to mitochondrion 1
SEX4
Starch Excess 4
TCPTP
T-cell protein tyrosine phosphatase
VHR
VH1-related dual-specificity phosphatase

Footnotes

Competing Interests

The authors declare no competing interests.

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