Generation of a Polyclonal Antibody against the Mouse Metal Transporter ZIP8

ZIP8 is a newly identified metal transporter. In human patients, mutations in ZIP8 result in severe manganese deficiency, suggesting a critical role for ZIP8 in regulating systemic manganese homeostasis. In mice, the deletion of ZIP8 recapitulates the symptoms of patients with ZIP8 mutations. However, further studies using mouse models to examine ZIP8′s function were hindered by the lack of suitable antibodies to detect endogenous ZIP8 protein. In this study, we report the design, generation, and validation of a polyclonal antibody against mouse ZIP8. We have demonstrated that the newly generated antibody can be reliably used in immunoblotting analysis to detect endogenous ZIP8 protein in mouse tissues. The successful generation and validation of anti-mouse ZIP8 antibody provide opportunities to further examine the function and regulation of this metal transporter. In addition, our study may provide valuable insights into the future development of antibodies targeting polytopic membrane proteins.


Introduction
Antibodies serve as critical tools in a variety of biological research, including the examination of nutrient metabolism. As an essential nutrient, manganese is required for different cellular processes, including gluconeogenesis, protein glycosylation, urea formation, and mitochondrial antioxidant defense [1][2][3]. To carry out these fundamental functions, manganese needs to be imported into the cells by metal transporters. ZIP8 is a polytopic membrane protein that facilitates manganese accumulation in cells [4][5][6]. In humans, mutations in ZIP8 cause severe manganese deficiency, indicating that ZIP8 plays an important role in regulating physiological processes relevant to systemic manganese homeostasis. However, the precise function of ZIP8 in manganese metabolism remains to be determined.
Similarly to patients carrying ZIP8 mutations, Zip8 knockout (Zip8 -/-) mice developed manganese deficiency, suggesting that mice could serve as an animal model to further study ZIP8 s function. To study the function and regulation of proteins, immunoblotting analysis is commonly used for the measurement of protein expression. This assay requires a probe antibody that can recognize the protein of interest. Due to the lack of reliable antibodies that could effectively detect endogenous mouse ZIP8 (mZIP8) in immunoblotting assays, prior studies mainly used epitope-tagged variants of ZIP8 and ectopic expression systems to examine the levels of protein expression [4,6,7]. The knowledge about the expression and regulation of endogenous mZIP8 is limited. Therefore, it is of critical need to develop antibodies that can reliably detect mZIP8 in mouse tissues, to facilitate further investigations of the function and regulation of this metal transporter.
To generate antibodies, one frequently used approach is to produce a short peptide of 10 to 20 amino acids that is predicted to represent a region of the targeted protein [8][9][10]. The peptide needs to be further conjugated to a carrier protein, such as the keyhole limpet hemocyanin (KLH), to increase the immunogenicity. After administration into animals, the The sequences encoding serine 30 to serine 124 of mZIP8 were amplified by polymerase chain reaction (PCR) using pCMV-Entry-mZIP8 expression vector (Origene, Rockville, MD, USA) as the template. The following primer sets were used for amplification: mZIP8 forward 5 -ATA AA GGA TCC AAA GTG AGG ATG TGC TGA GCG T-3 ; reverse 5 -AAT ATG AAT TCT CAA CTG GGC TTT GCG TTG TGC-3 . To assist the cloning process, BamHI and EcoRI sites were added to the forward and reverse primers, respectively. The amplification products were loaded onto a 2% agarose gel for electrophoresis. The specific bands were excised from the gel, purified using Wizard SV Gel and PCR Clean-Up system (Promega, Fitchburg, WI, USA), digested with BamHI and EcoRI, and subsequently cloned into pGEX-3X vector (Addgene, Watertown, MA, USA) to produce the bacterial expression plasmid encoding mZIP8-GST fusion protein.

Expression and Purification of GST Fusion Proteins
To express the recombinant protein, the pGEX-3X plasmid encoding GST or mZIP8-GST fusion protein was transformed into Rosetta-2 strains of E. Coli. The antibiotic-resistant colony was selected and cultured at 37 • C. An aliquot of 500 µL overnight culture was diluted into 4 L of Luria-Bertani (LB) medium and cultured at 37 • C with shaking at 200 rpm. When the bacteria culture reached a density of 0.6 (OD 600 ), isopropyl-β-Dthiogalactoside (IPTG) was added to a final concentration of 1 mM to induce the expression of recombinant proteins. After 6 h of induction, the culture was centrifuged at 3500 rpm at 4 • C and the supernatant was discarded. The bacterial pellet was re-suspended in ice-cold cell lysis buffer (50 mM NaCl, 50 mM Tris, 5 mM EDTA, 1× protease inhibitor, pH 7.3) and lysed using a French press. The cell lysates were centrifuged in a JA-17 rotor at 11,000 rpm for 1 h at 4 • C to clear the cell debris, and then applied to the glutathione sepharose to allow the binding of GST or GST fusion protein. The elution buffer (0.1 M glycine-HCl, pH 2.5) was added to elute the bound proteins. Subsequently, proteins were concentrated using Amicon Ultra-4 centrifugal filters with a 10 kDa cut-off (Millipore, Burlington, MA, USA).

Affinity Purification of Antibodies
The immunization procedure was performed by the Pocono Rabbit Farm and Laboratory (Canadensis, PA, USA). The antisera were used to purify antigen-specific antibodies. To cross link GST and GST fusion proteins to the glutathione sepharose, a column with 2 mL sepharose (Cytiva, Marlborough, MA, USA) was equilibrated with 5 mL binding buffer (140 mM NaCl, 2.7 mM KCl, 10 mM Na 2 HPO 4 , 1.8 mM KH 2 PO 4 , pH 7.3). Pre-cleared bacterial lysates containing either GST or GST fusion proteins were incubated with the sepharose for 1 h at 4 • C. The column was then washed 3 times with binding buffer and allowed to drain completely after the last wash. To purify antibodies, 2 mL of anti-serum was incubated with GST-linked column that was pre-washed with 20 mL TBS (10 mM Tris/HCl, 150 mM NaCl, pH 7.50). After 1 h of incubation at 4 • C, the column was eluted by gravity flow and washed with 5 mL TBS. The eluate was then incubated with GST fusion protein-linked column for 1 h at 4 • C. The column was washed with 20 mL TBS and then 10 mL 0.1× TBS. Antibodies were eluted with 0.8 mL elution buffer into 1.5 mL tubes pre-loaded with 0.2 mL neutralization solution (50 mM Tris-HCl, pH 8.0). A total of 10 eluate fractions were collected for further analysis.

Cell Culture and Transfection
HEK 293 cells were grown in Dulbecco's Modified Eagle's Medium (DMEM, Sigma-Aldrich, St. Louis, MO, USA) with 4.5 g/L glucose, 4 mM L-glutamine, 1 mM sodium pyruvate, and 10% fetal bovine serum (FBS, VWR, Radnor, PA, USA), and maintained in an incubator with 5% CO 2 at 37 • C. Plasmids encoding FLAG-tagged mZIP8 (pCMV-Entry-hZIP8) was purchased from Origene. For transient transfection, cells were seeded at 40% confluency in 6-well culture plates. Transfection began 24 h after seeding with 0.4 µg of plasmid DNA, 3.2 µL of enhancer, and 10 µL of Effectene reagent (Qiagen, Germantown, MD, USA). Transfection was carried out for 48 h before further analysis. To knock down the expression of FLAG-tagged mZIP8 protein, 24 h after the plasmid transfection. siRNA targeting mouse ZIP8 (5 -GCG AGG AUC UAA GAA AGC ACA ACG C-3 ) was transfected using the Lipofectamine RNAiMAX transfection reagent (Thermo Fisher Scientific, Waltham, MA, USA). A scramble siRNA was used as the negative control. The siRNA transfection procedure was performed per the manufacturer's protocol using 30 pmol of siRNA and 9 µL of transfection reagent. Cell lysates were collected 24 h after the siRNA transfection.

Topological Analysis and Signal Peptide Prediction of mZIP8
The mZIP8 is a polytopic membrane protein. To select suitable sequences for the antigen production, the transmembrane regions and signal peptide sequences within a polytopic protein need to be avoided [27,28]. Therefore, to design the sequence for the antigen production, we first established the topology model for mZIP8 by using four computational programs HMMTOP, MEMSAT, TOPCONS, and SPOCTOPUS. These four programs have been previously reported to retain high levels of accuracy for topological prediction [29]. For mZIP8 protein, the programs HMMTOP, MEMSAT, and TOPCONS predicted six transmembrane domains with four extracellular and three cytoplasmic loops, whereas the program SPOCTOPUS predicted eight transmembrane helices with five extracellular and four cytoplasmic loops ( Figure 1A). Furthermore, all four programs consistently predicted the presence of an extended extracellular amino terminus (N terminus) and a cleavable signal peptide sequence near the start of mZIP8's amino acid sequence with only minor variations in the predicted cleavage sites ( Figure 1A). We avoided the signal peptide sequence and transmembrane helices, and selected the N-terminal extracellular region of mZIP8 for the antigen production ( Figure 1B).

Construction of the Plasmid Expression and Purification of the GST Fusion Protein as the Antigen
To facilitate the production and purification of antigen, the N-terminal sequence encoding serine 30 to serine 124 of mZIP8 (NT-mZIP8) was cloned into a pGEX-3X vector to allow the expression of the GST fusion protein. GST naturally occurs as a roughly 26 kDa protein ( Figure 2A); the expected size of recombinant GST-NT-mZIP8 was predicted to be ~41 kDa ( Figure 2B). After vector construction, the pGEX-3X plasmids encoding the GST fusion protein were transformed into E. Coli. The transformed bacteria were then cultured with 1 mM IPTG to induce the expression of GST fusion proteins. The lysates from IPTG-induced culture were assessed by SDS-PAGE, and the lysate without induction was used as the control to confirm the successful induction of GST fusion protein.
The GST-NT-mZIP8 fusion protein was subsequently purified using immobilized glutathione sepharose column and analyzed by SDS-PAGE. Coomassie blue staining was applied to assess the identity of purified antigen. The band of the recombinant GST-NT-

Construction of the Plasmid Expression and Purification of the GST Fusion Protein as the Antigen
To facilitate the production and purification of antigen, the N-terminal sequence encoding serine 30 to serine 124 of mZIP8 (NT-mZIP8) was cloned into a pGEX-3X vector to allow the expression of the GST fusion protein. GST naturally occurs as a roughly 26 kDa protein ( Figure 2A); the expected size of recombinant GST-NT-mZIP8 was predicted to be~41 kDa ( Figure 2B). After vector construction, the pGEX-3X plasmids encoding the GST fusion protein were transformed into E. Coli. The transformed bacteria were then cultured with 1 mM IPTG to induce the expression of GST fusion proteins. The lysates from IPTG-induced culture were assessed by SDS-PAGE, and the lysate without induction was used as the control to confirm the successful induction of GST fusion protein. The GST-NT-mZIP8 fusion protein was subsequently purified using immobilized glutathione sepharose column and analyzed by SDS-PAGE. Coomassie blue staining was applied to assess the identity of purified antigen. The band of the recombinant GST-NT-mZIP8 at the corresponding molecular size around 41 kDa could predominantly be observed in the SDS-PAGE gel (Figure 3), confirming the presence of desired antigen product. mZIP8 at the corresponding molecular size around 41 kDa could predominantly be observed in the SDS-PAGE gel (Figure 3), confirming the presence of desired antigen product.  After adding IPTG to the culture at a final concentration of 1 mM, the culture was grown for an additional 3 h. Cells were lysed, and the lysates were applied to the glutathione sepharose to allow the binding of GST fusion proteins. The elution buffer was added to elute the GST fusion proteins (10 consecutive fractions of the eluate were collected, 1 mL/fraction). SDS-PAGE gel loaded with different fractions of GST-mZIP8 was stained with Coomassie blue.

Purification of Anti-mZIP8 Antibody
To generate antigen-specific polyclonal antibody, rabbits were immunized with purified GST-NT-mZIP8 according to the standard procedure (Performed in the Pocono Rabbit Farm and Laboratory). Seventy days after the immunization, rabbit antisera were collected and affinity chromatography was used for the antibody purification [30]. Anti-GST antibodies were first depleted by affinity purification using GST-immobilized glutathione sepharose. The unbound flow-through from the GST column was collected and subsequently passed three times over the sepharose column-linked with GST-NT-mZIP8 to allow the binding of anti-mZIP8 antibodies ( Figure 4A). The bound antibodies were   After adding IPTG to the culture at a final concentration of 1 mM, the culture was grown for an additional 3 h. Cells were lysed, and the lysates were applied to the glutathione sepharose to allow the binding of GST fusion proteins. The elution buffer was added to elute the GST fusion proteins (10 consecutive fractions of the eluate were collected, 1 mL/fraction). SDS-PAGE gel loaded with different fractions of GST-mZIP8 was stained with Coomassie blue.

Purification of Anti-mZIP8 Antibody
To generate antigen-specific polyclonal antibody, rabbits were immunized with purified GST-NT-mZIP8 according to the standard procedure (Performed in the Pocono Rabbit Farm and Laboratory). Seventy days after the immunization, rabbit antisera were collected and affinity chromatography was used for the antibody purification [30]. Anti-GST antibodies were first depleted by affinity purification using GST-immobilized glutathione sepharose. The unbound flow-through from the GST column was collected and subsequently passed three times over the sepharose column-linked with GST-NT-mZIP8 to allow the binding of anti-mZIP8 antibodies ( Figure 4A). The bound antibodies were vector was diluted in fresh LB media and grown for 1 h. After adding IPTG to the culture at a final concentration of 1 mM, the culture was grown for an additional 3 h. Cells were lysed, and the lysates were applied to the glutathione sepharose to allow the binding of GST fusion proteins. The elution buffer was added to elute the GST fusion proteins (10 consecutive fractions of the eluate were collected, 1 mL/fraction). SDS-PAGE gel loaded with different fractions of GST-mZIP8 was stained with Coomassie blue.

Purification of Anti-mZIP8 Antibody
To generate antigen-specific polyclonal antibody, rabbits were immunized with purified GST-NT-mZIP8 according to the standard procedure (Performed in the Pocono Rabbit Farm and Laboratory). Seventy days after the immunization, rabbit antisera were collected and affinity chromatography was used for the antibody purification [30]. Anti-GST antibodies were first depleted by affinity purification using GST-immobilized glutathione sepharose. The unbound flow-through from the GST column was collected and subsequently passed three times over the sepharose column-linked with GST-NT-mZIP8 to allow the binding of anti-mZIP8 antibodies ( Figure 4A). The bound antibodies were eluted using antibody elution buffer. A total of ten sequential fractions from the final eluate, together with the initial antisera, were evaluated by Coomassie blue staining of SDS-PAGE gels performed under reducing conditions. The anti-mZIP8 antibody appeared abundantly at an apparent molecular mass of~50 kDa, corresponding to the heavy chain of IgG, and the lower~25 kDa bands could represent the IgG light chains ( Figure 4B). Fractions 2, 3, and 4 of the final eluate appeared to contain higher amounts of antibodies, and were used for further antibody validation experiments. odies 2021, 10, x FOR PEER REVIEW 7 of 13 eluted using antibody elution buffer. A total of ten sequential fractions from the final eluate, together with the initial antisera, were evaluated by Coomassie blue staining of SDS-PAGE gels performed under reducing conditions. The anti-mZIP8 antibody appeared abundantly at an apparent molecular mass of ~50 kDa, corresponding to the heavy chain of IgG, and the lower ~25 kDa bands could represent the IgG light chains ( Figure 4B). Fractions 2, 3, and 4 of the final eluate appeared to contain higher amounts of antibodies, and were used for further antibody validation experiments.

Validation of Antibodies in Cells with Ectopic Overexpression of mZIP8
Proper antibody validation for the immunoblotting assay is to demonstrate that an antibody can detect its target protein when bound to immobilization membranes [31]. To evaluate the specificity of anti-mZIP8 antibody, we first performed immunoblotting analysis of HEK293 cells overexpressing FLAG-tagged mZIP8. The anti-mZIP8 antibody detected primarily two bands, similar to the band pattern detected by the anti-FLAG antibody ( Figure 5A). The 50 kDa band represents the predicted molecular mass of mZIP8 and the band at ~150 kDa may correspond to a multimer form of mZIP8.
To further determine the specificity of the mZIP8 antibody, we transiently transfected HEK293 cells with a plasmid encoding FLAG-tagged mZIP8. After plasmid transfection, cells were transfected with either negative control or mZIP8-targeting siRNA. Immunoblotting results indicate that siRNA transfected cells had a marked reduction in ZIP8 expression detected by the anti-mZIP8 antibody, verifying that the signals detected by the antibody indeed represent mZIP8 ( Figure 5B). Rabbit antisera were diluted in binding buffer. The diluted sera were first applied to GST-linked sepharose column (GST column) three times to deplete anti-GST antibodies. The flow-through (flow-through 1) was then applied to the GST-NT-mZIP8-linked sepharose column (GST-mZIP8 column) to allow the binding of anti-mZIP8 antibody. The flow-through (flow-through 2) was discarded and the elution buffer was applied to elute antibodies (10 sequential fractions were collected, 1 mL/fraction). (B) Coomassie staining of SDS-PAGE gel loaded with different fractions of anti-mZIP8 antibodies, together with the original antiserum. The pooled antibodies from fractions 2, 3, and 4 were further used for antibody validation experiments.

Validation of Antibodies in Cells with Ectopic Overexpression of mZIP8
Proper antibody validation for the immunoblotting assay is to demonstrate that an antibody can detect its target protein when bound to immobilization membranes [31]. To evaluate the specificity of anti-mZIP8 antibody, we first performed immunoblotting analysis of HEK293 cells overexpressing FLAG-tagged mZIP8. The anti-mZIP8 antibody detected primarily two bands, similar to the band pattern detected by the anti-FLAG antibody ( Figure 5A). The 50 kDa band represents the predicted molecular mass of mZIP8 and the band at~150 kDa may correspond to a multimer form of mZIP8.

The Anti-mZIP8 Antibody Can Recognize Endogenous Protein in Mouse Tissues
The use of cells that overexpress the antibody's target protein provides useful information about the specificity of antibody, but the use of tissues from gene knockout animals serves as a fundamental approach to demonstrate whether the antibody can detect the endogenous protein [32]. Due to the lack of suitable antibodies, previous immunoblotting analyses that convincingly demonstrate endogenous ZIP8 protein expression in mouse tissues are limited. Therefore, we collected tissue samples from wild-type (WT) and Zip8 -/-mice to further carry out antibody validation. We found that the anti-mZIP8 antibody detects endogenous ZIP8 in the mouse lung at around 150 kDa, and that this immunoreactive band deceases in the tissue from Zip8 -/-mice, further verifying the specificity of anti-mZIP8 antibody ( Figure 6). The detected band size of ~150 kDa is consistent with a previous report that in human lung epithelial A549 cells, the endogenous ZIP8 is detected only at ~150 kDa [33]. To further determine the specificity of the mZIP8 antibody, we transiently transfected HEK293 cells with a plasmid encoding FLAG-tagged mZIP8. After plasmid transfection, cells were transfected with either negative control or mZIP8-targeting siRNA. Immunoblotting results indicate that siRNA transfected cells had a marked reduction in ZIP8 expression detected by the anti-mZIP8 antibody, verifying that the signals detected by the antibody indeed represent mZIP8 ( Figure 5B).

The Anti-mZIP8 Antibody Can Recognize Endogenous Protein in Mouse Tissues
The use of cells that overexpress the antibody's target protein provides useful information about the specificity of antibody, but the use of tissues from gene knockout animals serves as a fundamental approach to demonstrate whether the antibody can detect the endogenous protein [32]. Due to the lack of suitable antibodies, previous immunoblotting analyses that convincingly demonstrate endogenous ZIP8 protein expression in mouse tissues are limited. Therefore, we collected tissue samples from wild-type (WT) and Zip8 -/mice to further carry out antibody validation. We found that the anti-mZIP8 antibody detects endogenous ZIP8 in the mouse lung at around 150 kDa, and that this immunoreactive band deceases in the tissue from Zip8 -/mice, further verifying the specificity of anti-mZIP8 antibody ( Figure 6). The detected band size of~150 kDa is consistent with a previous report that in human lung epithelial A549 cells, the endogenous ZIP8 is detected only at~150 kDa [33]. Figure 6. Validation of the anti-mZIP8 antibody using tissues from Zip8 knockout mice. The anti-mZIP8 antibody was used in the immunoblotting (IB) assay to detect endogenous ZIP8 in the lungs of wild-type (WT) and Zip8 -/-mice. GAPDH was used as the loading control.
The liver and small intestine are two major organs involved in regulating systemic manganese homeostasis [34]. Previous studies have determined that the mRNA level of ZIP8 is highest in the lung [5,35]. However, the protein levels of ZIP8 in the lung, liver, and small intestine have not been examined. The generation of anti-mZIP8 antibody allowed us to further compare ZIP8 protein expression in different mouse tissues using the immunoblotting assays. We revealed that, in contrast to ZIP14 which is highly expressed in the liver and small intestine, ZIP8 protein is highly enriched in the lung, but not in the liver or small intestine ( Figure 7A,B). This finding may suggest a distinct role for ZIP8 in manganese metabolism of the lung.
Together, the anti-mZIP8 antibody generated in this study could be consistently applied in the immunoblotting assays to detect the endogenous mZIP8 protein, and would serve as a valuable tool for further studies involving the detection of mZIP8 protein at tissue levels. Figure 6. Validation of the anti-mZIP8 antibody using tissues from Zip8 knockout mice. The anti-mZIP8 antibody was used in the immunoblotting (IB) assay to detect endogenous ZIP8 in the lungs of wild-type (WT) and Zip8 -/mice. GAPDH was used as the loading control.
The liver and small intestine are two major organs involved in regulating systemic manganese homeostasis [34]. Previous studies have determined that the mRNA level of ZIP8 is highest in the lung [5,35]. However, the protein levels of ZIP8 in the lung, liver, and small intestine have not been examined. The generation of anti-mZIP8 antibody allowed us to further compare ZIP8 protein expression in different mouse tissues using the immunoblotting assays. We revealed that, in contrast to ZIP14 which is highly expressed in the liver and small intestine, ZIP8 protein is highly enriched in the lung, but not in the liver or small intestine ( Figure 7A,B). This finding may suggest a distinct role for ZIP8 in manganese metabolism of the lung. GAPDH was used as the loading control. The kidney samples were used in both (A,B) to serve as a tissue control because both ZIP8 and ZIP14 can be detected in the WT mouse kidney. Our results indicate that ZIP8 protein is highly expressed in the lung, and that ZIP14 is enriched in both the liver and small intestine.

Discussion
Antibodies are among the most frequently used reagents in biological research. In this study, we report on the production and validation of an antibody against the mouse metal transporter ZIP8. ZIP8 is a polytopic membrane protein. Studies using in vitro cell cultures and epitope-tagged ZIP8 variants have revealed that ZIP8 can mediate the influx Figure 7. ZIP8 protein is enriched in the lung, but not in the liver or small intestine. The lung, kidney and (A) liver or (B) small intestine from wild-type (WT) and Zip8 -/or Zip14 -/mice were homogenized and analyzed by immunoblotting (IB). GAPDH was used as the loading control. The kidney samples were used in both (A,B) to serve as a tissue control because both ZIP8 and ZIP14 can be detected in the WT mouse kidney. Our results indicate that ZIP8 protein is highly expressed in the lung, and that ZIP14 is enriched in both the liver and small intestine.
Together, the anti-mZIP8 antibody generated in this study could be consistently applied in the immunoblotting assays to detect the endogenous mZIP8 protein, and would serve as a valuable tool for further studies involving the detection of mZIP8 protein at tissue levels.

Discussion
Antibodies are among the most frequently used reagents in biological research. In this study, we report on the production and validation of an antibody against the mouse metal transporter ZIP8. ZIP8 is a polytopic membrane protein. Studies using in vitro cell cultures and epitope-tagged ZIP8 variants have revealed that ZIP8 can mediate the influx of manganese into cells [4,6,36]. In humans, mutations in ZIP8 lead to severe manganese deficiency [37][38][39], indicating that the primary function of ZIP8 is to regulate body manganese metabolism. However, the precise process and mechanisms of this regulation have not been fully determined.
Mouse models are widely used to provide insights into the mechanisms underlying human disorders [40]. Recently, it has been reported that the Zip8 -/mice recapitulate the key symptoms of patients with ZIP8 mutations [41], and therefore could serve as an invaluable tool for the understanding of mechanisms underlying human disorders associated with the loss of ZIP8. However, the use of mouse models to further investigate the function and regulation of ZIP8 was hindered by lack of reliable antibodies that can consistently detect endogenous mZIP8 protein.
To generate an antibody for mZIP8, we performed bioinformatic analyses to determine a base amino acid sequence for the design of an antigen. After identifying the potential signal peptide cleavage site, the N-terminal extracellular region of mZIP8 covering about 100 amino acids was selected and cloned into the pGEX-3X vector to produce a GST fusion protein for immunization. This strategy was taken for two reasons: first, the terminal region sequences are more immunogenic compared to core peptides [10,11]; second, because of the relatively larger sizes, GST fusion proteins typically contain more potentially immunogenic epitopes than the synthetic short peptides. Using this approach, we successfully generated a polyclonal anti-mZIP8 antibody. We also provided convincing results to demonstrate that this antibody can be reliably applied in immunoblotting assays to detect both mZIP8 ectopically expressed in cells and endogenous mZIP8 protein in mouse tissues. Therefore, this newly generated antibody will serve as a valuable tool to study the function and regulation of ZIP8 using immunoblotting assays. Future studies are needed to evaluate whether this antibody could be used in other antibody-based assays, such as immunohistochemistry and immunoprecipitation analyses.
From a practical standpoint, this strategy of generating an anti-mZIP8 antibody was based on a combination of bioinformatic analyses and the production of a GST fusion protein [20,42,43]. This approach can be directly used by other general laboratories. A similar approach was used to generate an anti-human ZIP8 antibody by Zang et al. [44]. Since antibodies are critical to many types of research, our results may offer valuable insights into the future development of antibodies against polytopic membrane proteins, especially for those with extended terminal domains.