Characterization of Novel Human β-glucocerebrosidase Antibodies for Parkinson’s Disease Research

Cell culture

H4 cells were maintained in DMEM with GlutaMAX (Gibco, cat no: 10566016), supplemented with Sodium Pyruvate (Gibco, cat no: 11360070) and 10% Fetal Bovine Serum (R&D, cat no: S12450) in 6-well tissue culture plates. Human fibroblasts with the GBA1 genotypes wild-type/wild-type, N370S/N370S, and L444P/L444P were cultured in DMEM with GlutaMAX (Gibco, cat no: 10566016) with 15% Fetal Bovine Serum (R&D, cat no: S12450). Cells were kept in a 37°C incubator at 5% CO₂. A full media change was performed every 2–3 days and cells were split by dissociation with TrypLE Express Enzyme (Gibco, cat no: 12605010).

H4 cell pellet preparation

Cells were washed in PBS, dissociated with TrypLE Express Enzyme, quenched with cell media, and spun down at 500×g for 5 min. Cells were resuspended in PBS, transferred to a microcentrifuge tube, re-pelleted at 500×g for 5 min, and PBS was discarded. Pellets were flash frozen in dry ice and stored at –80°C for subsequent experiments.

GBA1–/–human neurons

A GBA1–/–hESC line was previously generated and characterized [8]. Neural precursor cells (NPCs) were generated from the hESCs using a modified dual SMAD inhibition protocol [9], as previously described [10, 11]. For neuronal differentiation, NPC were dissociated with 0.05% trypsin-EDTA (ThermoFisher, Cat. 25300054) and plated on poly-L-ornithine/laminin (PLO)-coated dishes at a density of 10,000–15,000 cells/cm2 in N2B27 medium supplemented with 100 ng/ml FGF-8 (PeproTech, Cat.100-25), 200 ng/ml sonic hedgehog (PeproTech, Cat. 100-45), and 100μM ascorbic acid 2-phosphate (Sigma, Cat. A8960-5G) for seven days. Finally, the NPCs were plated on PLO-coated plates at a density of 50,000 cells/cm² in BGAA medium, which was composed of N2B27 medium supplemented with 20 ng/ml BDNF (R&D System, Cat. 248-BDB-01M/CF), 10 ng/ml GDNF (PeproTech, Cat. 450-10), 500μM Dibutyryl-cAMP (STEMCELL Technologies, Cat. 100-0244), and 100μM ascorbic acid 2-phosphate (Sigma, Cat. A8960-5G). Neuronal cultures were maintained in BGAA medium for 6 weeks, and the cell culture medium was changed every 4 days.

Sanger sequencing

Genomic DNA was extracted from H4 cell pellets with Machery-Nagel genomic DNA extraction kit according to manufacturer instructions (cat no: 740952.250). Primers flanking exon 4 and exon 5 of GBA1 were ordered from IDT. Sequence for forward primer (P1) is aaggcaggtctcaaactcctcac (5’ to 3’) and for reverse primer (P2) is agaatgggcagagtgagattctgc (5’ to 3’). The PCR mix was prepared by combining Ampligold Taq Mastermix (cat no: 439888) without GC enhancer with 0.5 pM of each primer, 0.5μg of genomic DNA. PCR was programmed to the following conditions: 95°C 10 min for 1 cycle; 95°C 30 s, 57°C 1 min, 72°C 1 min for 40 cycles; 72°C 7 min for 1 cycle and held at 4°C. A single specific band corresponding to the 761 bp amplicon was observed following DNA electrophoresis. PCR purification was performed with the QIAquick PCR Purification Kit (Qiagen, cat no: 28106) according to provided protocol. Sanger sequencing was prepared according to Genewiz Sample Submission guidelines using primers P1 or P2 mixed with PCR purification product. Sequencing results were analyzed using SnapGene software.

Protein lysate preparation for western blot

150–200μL of 1% Triton-X Lysis buffer [1% Triton X-100, 10% glycerol, 150 mM NaCl, 25 mM HEPES pH 7.4, 1 mM EDTA, 1.5 mM MgCl₂, supplemented with one EDTA-free protease inhibitor tablet per 10 mL of buffer (Pierce, cat no A32965)] was added to H4 pellets from three confluent wells of a 6-well plate. Pellets were pulse-sonicated at 420 Hz for 10 quick pulses and rested for 15–30 min on ice. Then, the cells were centrifuged for 15 min at 13000 xg at 4°C and the supernatant containing lysate was collected in a new tube. Protein concentration was determined by Pierce BCA Protein Assay kit (ThermoScientific, cat no: 23225) and lysates were stored in –80°C.

Resorufin β-D-glucopyranoside GCase assay

5×10⁴ H4 cells were washed once with PBS and lysed in 30μl GCase lysis buffer (0.05 M citric acid, 0.05 M KH2PO4, 0.05 M K2HPO4, 0.11 M KCl, 0.01 M NaCl, 0.001 M MgCl2, pH 6.0 with 0.1% (v/v) TritonX-100, supplemented with freshly added protease inhibitor). 10μl of cell lysate were mixed with 10μl of 10 mM resorufin-β-D-glucopyranoside and baseline fluorescence was measured at t₀ immediately. The build-up of fluorescent product (resorufin) was measured after incubation for 2 h at 37°C (λ _ex  = 535 nm and λ _em  = 595 nm) indicating GCase activity. Data was normalized to total protein levels and depicted as a percentage of untreated GBA1 WT cells.

Liquid chromatography-mass spectrometry analysis of GluSph

The following analytes and internal standards were purchased from Avanti Polar Lipids:

D-glucosyl-β-1-1’-D-erythro-sphingosine (GluSph (d18 : 1); #860535) and D-glucosyl-β-1-1’-D-erythro-sphingosine-d5 as internal standard 1 (GluSph-d5 (d18 : 1); #860636); D-galactosyl-β-1-1’-D-erythro-sphingosine (GalSph (d18 : 1); #860537) and D-galactosyl-β-1-1’-D-erythro-sphingosine-d5 as internal standard 2 (GalSph-d5 (d18 : 1); #860637). For chromatography HPLC grade solvents as well as Millipore water was used. Acetonitrile (LiChrosolv #1.00030) and methanol (LiChrosolv #1.06007) were obtained from Supelco (Merck), ammonium acetate for mass spectrometry was purchased by Sigma-Aldrich (#73594).

Stock solutions for analytes and internal standards were prepared at 1 mM in DMSO and kept at –20°C. For further spiking solutions acetonitrile/water 9/1 (v/v) was used as solvent. Calibration solutions were prepared by serial dilution in acetonitrile/water 9/1 (v/v) containing 2% DMSO. The concentration ranged from C1 = 10μM to C9 = 0.0039μM.

Analysis was conducted on a LC-MS-MS system consisting of a Waters Xevo-TQ-S mass spectrometer connected to a complete Waters Acquity I-class UPLC system with a flow through needle sample manager using a mixture of acetonitrile/methanol/water 40/40/20 (v/v/v) as wash solvent. The auto-sampler temperature was set to 15 °C. The Xevo TQ-S instrument operated in positive ion electrospray mode with both quadrupoles tuned to unit mass resolution using nitrogen as nebulization- and desolvation gas. The nebulizer gas flow was set to 150 l/h and the desolvation gas flow to 800 l/h with a temperature of 500°C. Argon was used as collision gas at a flow rate of 0.15 ml/min. Analytes and internal standards were detected by multiple reaction monitoring mode (MRM) following the transitions m/z 462.3 to 282.3 and m/z 467.3 > 287.3 at a cone voltage of 30 V and a collision energy of 18 V.

Samples were analyzed on a BEH glycan amide column (100×2.1 mm, 1.7μm particle size, purchased from Waters, Switzerland) with a flow rate of 0.25 ml/min and an oven temperature of 30°C. Eluent A consisted of 100mM ammonium acetate and for eluent B acetonitrile was used. Glycospecific separation was achieved by isocratic elution with 90% B followed by a washing step with 10% B and column reconditioning. The overall analysis time was 12 min.

Sample preparation for in vitro GluSph measurements

50μl of distilled water were added to deep frozen cell pellets and samples were shaken for 30 min at 25°C until the cells thawed. Then, 100μl methanol containing 0.005μM internal standards was added. After shaking 5 min, the supernatant was transferred to a 96-well plate. Tubes were rinsed again with 100μl of methanol and supernatant was transferred to the same plate. The samples were evaporated to dryness and reconstituted in 100μl acetonitrile/water 90/10 (v/v) containing 1% DMSO and analyzed by LC-MS/MS. Lipids were quantified using the peak area ratio analyte/internal standard (= response).

Antibodies

Western blot: Conventional chemiluminescence platform

For each sample, 40μg of protein was loaded onto a 4–20% Mini-PROTEAN TGX PVDF gel (Bio-Rad Laboratories). After transfer with the Trans-Blot Turbo transfer system (Bio-Rad Laboratories), PVDF membranes (Bio-Rad Laboratories) were dried and reactivated with methanol. Methanol was rinsed off with water and TBST [1xTBS (from 10x TBS, 0.1% Tween] and the membrane was blocked for 1 h at RT with blocking solution [1×TBST, 5% (w/v) BSA (Sigma, cat no: A-7888)]. 5% (w/v) NFDM (Biorad, cat no: 1706404) blocking was also performed for each antibody; 5% BSA showed clearer bands and less background compared to 5% NFDM blocking for all antibodies. PVDF membranes were probed overnight at 4°C with primary antibodies in antibody diluent [2% (w/v) BSA, 1x TBST]. Primary antibodies were diluted so that each antibody had a final concentration of approximately 0.5μg/mL. PVDF membranes were washed 3×10 min at RT with TBST. This was followed by incubation with Goat HRP-coupled secondary anti-mouse IgG (Abcam, cat no: ab205719, 1 : 10K dilution) or anti-rabbit IgG (Abcam, cat no: ab 205718, 1 : 60K dilution) antibodies in antibody diluent. PVDF membranes were washed 3×10 min with TBST. The antigen–antibody complexes were detected with SuperSignal West Pico PLUS Chemiluminescent Substrate (ThermoScientific) using the ChemiDoc XRS + Imager System (Bio-Rad). Blots were exposed for 3 seconds.

Western blot: Automated capillary platform

Simple Western’s Fluorescence Separation Module kit and 12–230 kDa Fluorescence Separation Capillary Cartridges (cat no: SM-W004) were used to perform automated western blotting. Samples were prepared and loaded according to manufacturer instructions. Samples were prepared in 0.1x sample buffer (10x Sample Buffer diluted in water) and Fluorescence 5x Master Mix such that 5μg of protein was loaded per lane at a concentration of 1 mg/mL. Prepared samples in master mix as well as Biotinylated Ladder were boiled at 95°C for 10 min. All primary antibodies were diluted in the provided Antibody Diluent 2 at 1 : 50 dilution, except for R386 and GAPDH, which were diluted 1 : 1500 in Antibody Diluent 2. 10μL of diluted antibody was loaded in each lane. 10μL of HRP-conjugated mouse or rabbit secondary antibody was loaded to the corresponding lanes. Finally, 15μL peroxide-luminol mix was loaded into each lane, the cartridge was centrifuged for 5 min at 1000xg, and wash buffer was added according to the user manual. The cartridge and capillaries were loaded into the Jess instrument (ProteinSimple) and the loading times used were the default for HRP chemiluminescence detection. Results were visualized and analyzed with the Compass for Simple Western program.

Immunocytochemistry

Cells were seeded in 8-well imaging chambers at a density of 30K cells/chamber and grown for 48 h with daily feeding. After 48 h, cells were washed once in PBS and fixed in 4% paraformaldehyde (20 min, RT). Fixed cells were washed in PBS three times and incubated in primary antibody ICC antibody diluent [0.05% Saponin (filtered) and 1% BSA in PBS] overnight at 4°C. Wells were washed three times with PBS, followed by 3×5 min washes with PBS, then covered with aluminum foil and incubated with secondary antibody diluted in ICC antibody diluent in RT. Three PBS wash and 3 × 5 min washes in PBS were repeated, and cells were stored in PBS with NucBlue Fixed Cell ReadyProbes Reagent (DAPI) (ThermoFisher, cat no: R37606) in 4°C until imaging. Confocal images were acquired using a Zeiss LSM 880 confocal microscope using the 63x oil objective.

AlphaLISA

One million H4 cells were washed once with PBS and lysed in 80μl GCase lysis buffer (0.05 M citric acid, 0.05 M KH2PO4, 0.05 M K2HPO4, 0.11 M KCl, 0.01 M NaCl, 0.001 M MgCl2, pH 6.0 with 0.1% (v/v) TritonX-100, supplemented with freshly added protease inhibitor). Samples were diluted 1/5 or 1/10 in 1X Immunoassay buffer (Perkin Elmer, #AL000F). A 2-fold serial dilution of imiglucerase (Genzyme) ranging from 1250 pM –2.4 pM was generated as a standard curve. 10μl of samples or standards were incubated for 4 h at RT in the dark with 1 nM of biotinylated hGCase-1/23 and 20μg/ml of hGCase-1/17-conjugated Acceptor beads (beads:antibody 50 : 1). Subsequently, 40μg/ml of AlphaScreen Streptavidin Donor beads (Perkin Elmer, #6760002) were added and incubated 1 h at RT in the dark. Plate was read on a Tecan Spark plate reader with ex: 680 nm and em: 520–620 nm. GCase concentration was calculated based on a sigmoidal non-linear regression of the imiglucerase standard and then normalized to total protein concentration.

Immunoprecipitation

For immunoprecipitation, the Dynabeads™ Protein A Immunoprecipitation Kit (Thermo Fisher, #10006D) was used. 10μg of hGCase-1/17 or hGCase-1/23 or mouse IgG (Merck Millipore, #NI03) were coupled to 50μl of Protein A magnetic Dynabeads in 200μl Ab Binding and Washing Buffer for 30 min at RT on a rotating wheel. Subsequently, supernatant was removed, and Ab-conjugated beads were mixed with 100μg of cell lysate and incubated for 1 h at RT on a rotating wheel (20μg of cell lysate were saved for analysis). After incubation, supernatant (= flowthrough, FT) was saved for analysis and beads were washed 3 times in 200μl Washing Buffer. For elution, beads were resuspended in 20μl of Elution Buffer mixed with 7μl of 4X LDS sample buffer (Thermo Fisher, # NP0007) and 3μl of 10X reducing agent (Thermo Fisher, # NP0004) and heated for 10 min to 70°C. Supernatant (= elution) was saved for analysis. Samples were analysed by SDS-PAGE loading 10μl of each fraction per lane (lysate and FT were mixed with appropriate volumes of 4X LDS sample buffer and 10X reducing agent prior to loading). Proteins were transferred to a nitrocellulose membrane using the iBlot 2 device and membranes were blocked for 1 h at RT in 5% (w/v) Blotting Grade Blocker/PBS (Biorad, #170-6404). GCase was detected using rb mAb to hGBA antibody (abcam, #128879, clone EPR5143(3)) at 1/1000 in blocking solution. After 3×5 min washes in PBS, membranes were incubated with goat anti-rabbit HRP-labelled antibody (Perkin Elmer, # NEF812001EA) at 1/10000 in 1 % (w/v) Blotting Grade Blocker/PBS for 1.5 h at RT. Proteins were detected using the SuperSignal West Dura Extended Duration Substrate Kit (Thermo Fisher, #34076).

Development of monoclonal antibodies against human β-glucocerebrosidase

Mice were immunized with imiglucerase (Cerezyme, Sanofi), the recombinant hGCase produced in Chinese hamster ovary cells for enzyme replacement therapy (ERT) in patients with GD [12]. Among the screened hybridoma clones, hGCase-1/17 and hGCase-1/23 exhibited selectivity for hGCase in initial screening assays including western blotting and immunofluorescence in HEK293-F cells overexpressing hGCase (Supplementary Figure 1). Notably, hGCase-1/23 demonstrated superior potency compared to hGCase-1/17 in both western blot and immunofluorescence assays. Neither of these antibodies cross-reacted with mouse β-glucocerebrosidase (mGCase) overexpressed in HEK293-F cells in western blotting or immunofluorescence, underscoring their specificity for hGCase over mGCase.

Generation of GCase loss-of-function human neuroglioma H4 cells

To support further hGCase-1/17 and hGCase-1/23 characterization, a GCase loss-of-function (GBA1^–/–) human neuroglioma H4 line was generated. H4 (ATCC HTB-148) is a hypertriploid cell line with the modal chromosome number ranging from 63 to 78, with most cells having three copies of chromosome 1 and GBA1 alleles. To disrupt the multiple GBA1 alleles in the H4 cell genome, zinc-finger nuclease (ZFN)-mediated cleavage was combined with targeted integration of a gene disruption cassette into exon 4 of GBA1 alleles, following the workflow developed previously [8]. This targeting approach introduced a puromycin resistance cassette into one of the GBA1 alleles (Fig. 1A). H4 cells with the integrated resistance cassette were enriched using puromycin selection, followed by single cell cloning. Established single cell clones were screened for the resistance cassette by PCR and subsequently with an in vitro GCase activity assay using fluorogenic substrate resorufin-β-D-glucopyranoside (Res-Glc). The most promising clone underwent Sanger sequencing, confirming frameshift indels in the other two GBA1 alleles. A pair of PCR primers, P1 and P2, were designed to generate an amplicon of 761 bp, encompassing GBA1 exons 4 and 5 for Sanger sequencing. The GBA1 allele with the integrated puromycin resistance cassette could not produce PCR product due to the cassette’s size. The Sanger sequencing chromatogram of the chosen clone displayed double peaks near the Zinc-finger nuclease targeting site (Fig. 1B). Parsing the chromatogram with Poly Peak Parser (http://yost.genetics.utah.edu/software.ph) [13] indicated frameshift indels in the two GBA1 alleles that were targeted by ZFN, but without the resistance cassette integration (Supplementary Figure 2A). Given the disruption of all GBA1 alleles, this H4 clone is referred to as GBA1–/–, or the GCase knockout (KO) H4 line. The GBA1–/–H4 cells lacked GCase activity in the Res-Glc in vitro GCase activity assay (Fig. 1C). Corroborating the absence of GCase activity, the GBA1–/–H4 cells showed substantial GlcSph accumulation (Fig. 1D). Moreover, there were only minor changes in the GlcSph stereoisomer galactosylsphingosine (GalSph) in the GBA1–/–H4 cells, probably due to altered lysosomal homeostasis, indicating specific GBA1 targeting (Fig. 1E).

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Fig. 1

Generation of a GCase loss-of-function (GBA1–/–) human neuroglioma H4 line. A) Disruption of GBA1 alleles by targeting exon 4 with Zinc-finger nuclease (ZFN) and inserting a puromycin resistance cassette. Puromycin selection assisted with the enrichment of edited cells, which was followed by single cell cloning and validation by Sanger sequencing. B) Sanger sequencing chromatogram showing double peaks in the region near the ZFN targeting site, demonstrating the presence of frameshift indel mutations in two GBA1 alleles targeted by ZFN but lacking resistance cassette integration. C) Lack of GCase activity in GBA1–/–H4 cells as determined with the Res-Glc in vitro GCase activity assay (n = 3 biological replicates). D, E) Glucosylsphingosine and galactosylsphingosine levels in the GBA1 + /+ and GBA1–/–H4 cells (n = 5 biological replicates).

Benchmarking hGCase antibodies in traditional and automated capillary western blot

HGCase-1/17 and hGCase-1/23 were first evaluated by traditional western blotting using GBA1 + /+ and GBA1–/–H4 cell lysates. This assessment compared these new antibodies with three recent commercial hGCase antibodies not yet independently evaluated: mouse monoclonal IgG 812201 (R&D Systems, MAB7410), mouse monoclonal IgG 2E2 (Abcam, ab55080), rabbit monoclonal IgG EPR5143(3) (Abcam, ab128879), and the well-characterized in-house antibody rabbit polyclonal IgG R386 [14] (Table 1). While 2E2, EPR5143, and R386 detected specific hGCase bands in GBA1+ /+, but not GBA1–/–, cells in traditional western blots, 812201, hGCase-1/17, and hGCase-1/23 yielded unsatisfactory results despite extensive optimization (Fig. 2A and data not shown). Subsequently, hGCase antibodies were compared in an automated capillary western blotting system (Simple Western from ProteinSimple, Bio-Techne), which automates the protein separation and immunodetection steps in traditional western blot, thus minimizing error-prone steps. The three commercial antibodies and R386 successfully detected hGCase via automated capillary western blotting, indicating their compatibility with this approach (Fig. 2B). Notably, 812201 produced better results in capillary western blotting than in traditional westerns. However, hGCase-1/17 and hGCase-1/23 failed to detect endogenous hGCase in GBA1 + /+ cells using the capillary western blotting system. Hence, the three commercial hGCase antibodies were better suited for detecting endogenous hGCase in both traditional and capillary western blot. In contrast, hGCase-1/17 and hGCase-1/23 exhibited limited utility in western blot, detecting only overexpressed hGCase in HEK293-F cells (Supplementary Figure 1) but not at endogenous levels (Fig. 2).

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Fig. 2

Performance of hGCase antibodies in detecting endogenous hGCase in traditional and automated capillary western blotting. A) Traditional western blotting analyzing GBA1 + /+ and GBA1–/–H4 cell lysates with hGCase antibodies 812201, 2E2, EPR5143, R386, hGCase-1/17 and hGCase-1/23. B) Automated capillary western blotting analyzing GBA1 + /+ and GBA1–/–H4 cell lysates with hGCase antibodies. Note that 812201 detected endogenous hGCase in GBA1 + /+ H4 lysate in automated capillary western blotting.

Characterization of hGCase-1/17 and hGCase-1/23 through immunostaining

Among the three commercial hGCase antibodies, 2E2 and 812201 were marketed as suitable for immunostaining assays. However, independent evaluation of 2E2 through immunostaining using GBA1 + /+ and GBA1–/–SH-SY5Y cells yielded unsatisfactory results [15]. Consequently, hGCase-1/17 and hGCase-1/23 were compared with 812201 in immunostaining with paraformaldehyde (PFA)-fixed GBA1 + /+ and GBA1–/–H4 cells. Both hGCase-1/17 and hGCase-1/23 displayed substantial selectivity towards endogenous hGCase, with staining confined to vesicular and tubular lysosomes that co-stained with the lysosomal membrane protein LAMP1, correlating with the expected lysosomal localization of hGCase (Fig. 3A). Impressively, GBA1–/–H4 cells exhibited virtually no background. Although both antibodies were selective towards hGCase, hGCase-1/17 exhibited weaker staining compared to hGCase-1/23, indicating a lower potency (Fig. 3A). Additional assessments of hGCase-1/23 in human neurons differentiated from GBA1 + /+ and GBA1–/–human embryonic stem cell (hESC) lines further affirmed its specificity and potency (Fig. 3B). In contrast, 812201 failed to show specific staining in GBA1 + /+ H4 cells (Supplementary Figure 3). Therefore, hGCase-1/23 emerged as the recommended choice for immunofluorescence assays.

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Fig. 3

Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/–H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10μm, and 1.5μm in inserts. (B) GBA1 + /+ and GBA1–/–human neurons were stained with hGCase-1/23, together with LAMP1 and MAP2 antibodies. Scale bars: 100μm, and 25μm in inserts.

Evaluation of hGCase-1/23 with hGCase mutants through immunostaining

The effectiveness of hGCase-1/23 in immunostaining hGCase wild-type (WT) prompted further evaluation with hGCase mutants N370S and L444P that are common in patients with PD. Human fibroblasts expressing hGCase WT, N370S, and L444P were stained with hGCase-1/23. The antibody successfully detected both hGCase WT and N370S, revealing their presence within lysosomes marked by LAMP1 (Fig. 4, WT/WT and N370S/N370S). While the staining intensity notably decreased in L444P/L444P fibroblasts (Fig. 4, L444P/L444P), there was still a minimal presence of hGCase L444P/L444P detected in lysosomes (Fig. 4, L444P/L444P contrast adjusted). These findings collectively indicate that the epitope recognized by hGCase-1/23 remains largely unaffected by the amino acid changes in hGCase N370S and L444P mutations.

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Fig. 4

Immunostaining of hGCase WT, N370S, and L444P with hGCase-1/23. Fibroblasts from a healthy individual (WT/WT) and patients with GD (GBA1: N370S/N370S and L444P/L444P) were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and a LAMP1 antibody. Scale bars: 15μm, and 5μm in inserts.

Immunoprecipitation of hGCase using hGCase-1/17 and hGCase-1/23

Capitalizing on their success in recognizing external epitopes of hGCase in immunostaining, hGCase-1/17 and hGCase-1/23 were tested in immunoprecipitation assays for their ability to capture hGCase in cell lysates. Both antibodies effectively pulled down hGCase in GBA1 + /+ H4 cell lysates (Fig. 5A). Notably, hGCase-1/23 demonstrated superior capture efficiency than hGCase-1/17, in line with its superiority in the immunostaining assay (Fig. 5A). To further demonstrate their value in studying proteins interacting with hGCase, hGCase in human neuron lysates was captured with hGCase-1/23. Then, co-immunoprecipitated proteins were examined for the presence of lysosomal integral membrane protein-2 (LIMP-2/SCARB2), the trafficking receptor for hGCase [16–18]. LIMP-2 was co-immunoprecipitated with hGCase by hGCase-1/23 in GBA1 + /+, but not GBA1–/–, neuron lysates, indicating LIMP-2 co-immunoprecipitation relied on its interaction with endogenous hGCase (Fig. 5B).

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Fig. 5

Application of hGCase-1/17 and hGCase-1/23 in immunoprecipitation. A) HGCase in H4 cell lysates was immunocaptured with hGCase-1/17 or hGCase-1/23 and immunoblotted with hGCase antibody EPR5143 after elution. B) Co-immunoprecipitation of LIMP2 with hGCase by hGCase-1/23. hGCase in neuron lysates was immunocaptured with hGCase-1/23, and the presence of LIMP2 in GCase co-precipitates was detected with a LIMP2 antibody.

hGCase AlphaLISA assay with hGCase-1/17 and hGCase-1/23

The AlphaLISA (Amplified Luminescent Proximity Homogeneous Assay) is a bead-based luminescent amplification assay developed by PerkinElmer to detect and quantify biomolecules in diverse sample types (Fig. 6A). It offers a streamlined workflow, enhanced sensitivity, expansive dynamic range, and adaptability for high-throughput applications. In the AlphaLISA assay, a standard sandwich configuration employs two distinct antibodies recognizing non-overlapping epitopes on the target molecule. One biotinylated antibody is coupled with an Alpha streptavidin-coated Donor bead, while the other antibody is directly conjugated to the AlphaLISA Acceptor bead. When the analyte is present, the Donor and Acceptor beads come together. Upon excitation with a 680 nm laser, a photosensitizer inside the Donor bead converts ambient oxygen to an excited singlet state. Singlet oxygen diffuses up to 200 nm to produce a chemiluminescent reaction in the Acceptor bead, emitting light at 615 nm proportional to the analyte amount.

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Fig. 6

HGCase AlphaLISA assay. A) In the sandwich AlphaLISA assay, hGCase-1/23 was biotinylated and associated with the Alpha Donor Bead, and hGCase-1/17 was directly conjugated to the Alpha Acceptor Bead. B) Sensitivity and dynamic range of hGCase AlphaLISA assay (n = 3 technical replicates). C, D) Determination of hGCase levels in GBA1 + /+ and GBA1–/–H4 cells with hGCase AlphaLISA assay. A 2 h treatment with imiglucerase led to a dose-dependent increase in hGCase levels (C, n = 3 biological replicates; D, n = 4 to 12 technical replicates). E, F) Determination of hGCase levels in GBA1 + /+ and GBA1–/–human neurons with hGCase AlphaLISA assay. A 2 h treatment with imiglucerase led to a dose-dependent increase in hGCase levels (E, n = 3 biological replicates; F, n = 4 to 12 technical replicates).

The potential of hGCase-1/17 and hGCase-1/23 for the AlphaLISA assay was explored by generating a dose-response curve with imiglucerase. The AlphaLISA assay utilized a sandwich configuration where hGCase-1/23 was biotinylated and associated with the Alpha Donor Bead, and hGCase-1/17 was directly conjugated to the Alpha Acceptor Bead. This assay effectively quantified imiglucerase levels, exhibiting exceptional sensitivity, broad dynamic range, and substantial signal-to-background ratio (Fig. 6B). With this assay, hGCase protein per milligram of cell lysate was estimated at approximately 20 ng in GBA1 + /+ H4 cells and around 80 ng in GBA1 + /+ neurons, while GBA1–/–H4 or human neuron cell lysates showed no hGCase protein, underscoring the assay’s specificity towards hGCase (Fig. 6C, E). Imiglucerase treatment increased hGCase levels in H4 cells and human neurons, regardless of GBA1 genotype (Fig. 6D, F). This quantitative immuno-based assay has been previously employed to determine hGCase levels in PD and DLB postmortem brains [19].