Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm

Dengue is an arboviral disease, which threatens almost half the global population, and has emerged as the most significant of current global public health challenges. In this study, we prepared dengue virus-like particles (DENV-LPs) consisting of Capsid-premembrane-envelope (CprME) and premembrane-envelope (prME) polypeptides from serotype 1 and 4, which were expressed in the silkworms using Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid. 1CprME, 1prME, 4CprME, and 4prME expressed proteins in hemolymph, and the molecular weight of the purified proteins was 55 kDa, respectively. The purified polypeptides formed spherical Dengue virus-like particles (DENV-LPs) with ~ 30–55 nm in diameter. The immunoelectron microscopy (IEM) images revealed antigens to the surface of a lipid bilayer of DENV-LPs. The heparin-binding assay shows a positive relationship between absorbance and E protein domain III (EDIII) quantity, which is supported by the isothermal titration calorimetry assay. This indicates a moderate binding affinity between heparin and DENV-LP. The high correlation between patient sera and DENV-LP reactivities revealed that these DENV-LPs shared similar epitopes with the natural dengue virus. IgG elicitation studies in mice have demonstrated that DENV-LPs/CPrMEs elicit a stronger immune response than DENV-LP/prMEs, which lends credence to this claim. Supplementary Information The online version contains supplementary material available at 10.1186/s13568-022-01353-6.


Introduction
Dengue fever is a significant public health issue that has been reported in the Americas, Africa, Southeast Asia, Europe, the Western Pacific, and the Eastern Mediterranean. This arboviral disease is endemic in more than 100 countries, and approximately 96 million infected individuals have symptoms of varying severities. There has been a growing public health concern about dengue fever in the last few decades. The World Health Organization (WHO) named it one of the top ten global health threats in 2019, highlighting the critical need for a safe and effective vaccine. Despite numerous attempts, identifying the best candidate for a dengue vaccine continues to be a difficult task due to some critical factors that must be considered (Bhatt et al. 2021;Redoni et al. 2020).
Dengue virus (DENV) is the etiological agent for dengue fever. DENV belongs to the Flaviviridae family and Flavivirus genus. It has four antigenically distinct serotypes and antigenically similar yet genetically diverse.. Adaptive immunity induced by one DENV serotype does not provide long-term protection against infection with the other three heterotypic DENVs There is 70% sequence homology between DENV serotype 1-4 (DENV-1-DENV-4), which means that numerous immunogenic epitopes are conserved at some level. DENV is an enveloped virus with a single positive-strand RNA genome that encodes three structural proteins, Capsid (C), premembrane (prM), and envelope (E), as well as seven nonstructural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5) (Redoni et al. 2020;Yousaf et al. 2018).
Based on a 70-year study that examined the spread of DENV worldwide, the most reported strains were DENV-1, DENV-2, and DENV-3, and the least frequently recorded was DENV-4. Although DENV-4 was the first serotype of dengue to diverge in phylogenetic investigations of the Flavivirus genus, it spread slowly worldwide. DENV-1 and DENV-4 cause dengue fever with different degrees of severity. When DENV-1 infection was compared to DENV-4 infections, the duration of fever, which essentially correlates with the severity of the illness, was much longer for DENV-1. DENV-1 infection was also associated with more severe clinical manifestations than DENV-4 infection. Primary DENV-4 infection is a relatively mild sickness, but primary DENV-1 infection has more severe symptoms (Nishiura and Halstead 2007;Sang et al. 2019;Villabona-Arenas and Zanotto 2013).
Virus-like particles (VLPs) are viruses with a shell but no genetic material. VLPs may mimic the organization and conformation of wild viruses because they contain multiprotein determinants. The organization and conformation of native viruses can be used to explore virus infection mechanisms and stimulate the host immune system to produce robust immune responses (Roldao et al. 2010). Furthermore, VLPs do not cause infections because they lack the viral genome. These properties of VLPs make them potential vaccine candidates that may be more efficient and safer than conventionally attenuated or inactivated viruses (Noad and Roy 2003).
Two successful approaches have been applied to produce recombinant VLPs of flaviviruses, including capsid-premembrane-envelope (CprME) protein genes and pre-membrane-envelope (prME) proteins in cis as well as in trans from plasmid vectors. Both types of approaches should result in the formation of particles. Although the C protein is not required to form particles, the inclusion of C protein may have a stabilizing effect on VLP assembly. Capsid proteins can be arranged in one, two, or three layers, depending on their size. Some single-layer VLPs can contain more than one structural protein, whereas others cannot. When compared to the structure of single-protein VLPs (which is relatively simple), multiprotein VLPs (which contain several distinct capsid layers) have additional structural components (Krol et al. 2019;Nooraei et al. 2021). Baculovirus expression vector system (BEVS) is a high-level mass production tool for recombinant proteins in silkworm. This enables us to express eukaryotic recombinant proteins with posttranslational modifications similar to mammals' . The number of recombinant proteins produced by silkworm-BEVS in silkworm larvae is frequently significantly higher than that produced by Sf9-BEVS in cultured cells (Kato et al. 2010;Vipin Kumar Deo 2012). Feeding silkworms is exceptionally inexpensive, with a total cost of approximately USD 20 for twenty larvae. Thus, it costs slightly more than USD 20 to obtain approximately 1 mg of active Protein kinase B alpha (PKBα) (Maesaki et al. 2014). This approach is comparable in cost to an expression system based on Escherichia coli. Furthermore, because silkworms have low-cost productivity equal to the E. coli expression system, protein production can be quickly and inexpensively scaled up. This expression system is favorable for vaccine development (Fujita et al. 2020).
Previously, we have successfully expressed DENV-LPs serotype 2 (DENV-LP/2CprME and /2E) and DENV-LPs serotype 3 (DENV-LP/3prME and /3CprME) by removing capsid-anchor in the C region (Utomo et al. 2019(Utomo et al. , 2020. In this study, we prepared DENV-LPs consisting full-length of Capsid-Premembrane-Envelope (1CprME and 4CprME) and Premembrane-envelope (1prME and 4prME) polypeptides from serotypes 1 and 4, which were expressed using Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid in silkworms. We observed the formation of VLPs, confirmed envelope domain III (EDIII) of DENV using a heparin-binding assay by ELISA and ITC, reactivity toward dengue patient sera, and demonstrated the elicitation of antibody production in a mouse model.

Expression and purification
Ten fifth-stage instar silkworm larvae (Ehimesansyu) were injected with 100-fold diluted hemolymph in phosphate-buffered saline (PBS) (137 mM NaCl, 2.7 mM KCl, 8 mM Na 2 HPO 4 , and 2 mM KH 2 PO 4 , pH 7.4). They were fed a synthetic diet (Silkmate S2, Nosan Co., Yokohama, Japan). After 5 dpi, the hemolymph was collected by cutting the larva's leg. The hemolymph was diluted tenfold with 50 mM Tris-HCl (pH 7.5) containing 300 mM NaCl before being applied to DDDDK-tagged protein purification gel column chromatography (Medical & Biological Laboratories, Nagoya, Japan). The column was washed with 50 mM Tris-HCl (pH 7.5) containing 300 mM NaCl. The proteins were eluted with 0.17 M glycine-HCl buffer (pH 2.3). The eluents were neutralized immediately with 1 M Tris-HCl (pH 8.0). Ultrafiltration was used to concentrate the eluents using an Amicon Ultra-0.5 mL Centrifugal Filter Unit with an Ultracel-30 K membrane (Merck Japan, Tokyo, Japan). A BCA protein assay kit was used to determine the protein concentration (Thermo Fisher Scientific K. K.).

Western blot analysis
To separate the proteins, 10% or 12% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was used and subsequently subjected to western blotting by blotting the proteins trapped in acrylamide gel onto an Immobilon-P PVDF (polyvinylidene fluoride) membrane (Merck Japan) using the Mini Trans-Blot Electrophoretic Transfer Cell (Bio-Rad, Hercules, CA, USA). After blotting, the membrane was blocked in Tris-buffered saline with 0.1% Tween 20 detergent (TBST) (pH 7.6) with 5% skim milk (FUJIFILM Wako Pure Chemical). Then the membrane was incubated in 10,000-fold diluted mouse anti-HA tag antibody (Medical and Biological Laboratories) for DENV-1 constructs and anti-strap tag II antibody (Medical and Biological Laboratories) for DENV-4 constructs. Alternatively, 1500-fold diluted specific serotype monoclonal anti-envelope antibodies, anti-E DENV-1 E29 clone (BEI Resources, Virginia, US) for DENV-1 constructs, and anti-E DENV-4 E42 clone (BEI Resources) for DENV-4 constructs were used as the primary antibodies. Anti-E DENV-2 3H5-1 clone (BEI Resources) and anti-E DENV-3 E1 clone (BEI Resources) antibodies were also used to assess cross-reactivity between serotypes for all purified proteins. C protein was  also confirmed using an anti-capsid polyclonal antibody (GeneTex, CA, USA). After three washes with TBST, the membrane was incubated for one hour with 10,000-fold diluted anti-mouse IgG antibody conjugated to horseradish peroxidase (HRP) (FUJIFILM Wako Pure Chemical). The specific bands were discovered using a Fluor-S MAX Multi-Imager (Bio-Rad).

Heparin-binding assay by ELISA
The heparin-binding assay by ELISA was performed with modifications as previously described (Utomo et al. 2019(Utomo et al. , 2020. Six ng/ml diluted biotin-labeled heparin (Sigma-Aldrich Japan) and 1.8 ng of heparin were immobilized into blockless avidin plate (Sumitomo Bakelite, Tokyo, Japan) wells and washed three times with PBS. For negative control, 2 μg of BSA was used. Purified proteins of 1CprME, 1prME, 4CprME, and 4prME at various concentrations (0.5, 1, 5, and 10 g/ml) were added to wells at corresponding quantities, incubated at room temperature for one hour, and then washed with PBST. After serial washing, a 1000-fold diluted rabbit anti-DENV E polyclonal antibody (GeneTex) was added, followed by a 1000-fold diluted HRP-conjugated anti-rabbit IgG antibody (FUJIFILM Wako Pure Chemical). To stop the reaction, 100 μl of substrate 0.1 mg/ml 3.3′,5.5′-tetramethylbenzidine (TMB) in 100 mM sodium acetate (CH 3 COONa), pH 6.0, was added to each well with 0.2% (v/v) 30% hydrogen peroxide, and 50 μl of 1 N H 2 SO 4 was added. The absorbance was estimated at 450 nm.

Isothermal titration calorimetry assay for heparin-binding to DENV-LPs
The binding affinities of DENV-LP to heparin were determined using isothermal titration calorimetry (ITC) (MicroCal iTC200, Malvern Panalytical Ltd, Enigma Business Park, UK). Titrations were performed at a temperature of 25 °C by injecting 2 μl aliquots of 1000 μM ligand dissolved in 1 × PBS buffer into a cell containing 10 μM DENV-LP. The heat release was recorded, and the titration data were analyzed with MicroCal Origin ITC software (Malvern Panalytical Ltd). Thermodynamic parameters were determined by fitting experimental data with nonlinear least-squares using the one-set sites binding model (Duff et al. 2011;Ikegaya et al. 2021).

Human DENV-infected sera interaction with DENV-LPs
Direct ELISA was carried out with modifications as previously described (Utomo et al. 2019(Utomo et al. , 2020). An interaction between antigens, 1CprME, 1prME, 4CprME, and 4prME, and patient sera were detected using a direct ELISA method. Dengue patient sera [rapid diagnostic test NS1(+)] were used. Sera were obtained from the Centre of Pharmaceutical and Medical Technology, National Research and Innovation Agency, Jakarta, Indonesia. Protocols of the collection were reviewed and approved by the Health Research Ethics Committee-University of Indonesia and Cipto Mangunkusumo Hospital (HREC-FMUI/CMH) (approval no. KET-1358/UN2.F1/ETIK/ PPM.00.02/2020). Each diluted sample of 1CprME, 1prME, 4CprME, and 4prME, 100 µl of 20 ng/ml in coating buffer (0.05 M carbonate-bicarbonate, pH 9.6), was applied to a 96-well ELISA plate and incubated overnight at 4 °C. After incubation, the coating solution was discarded, and a 100 µl blocking solution (5% skim milk in PBS) was added to each well, followed by 1 h at 37 °C incubation. The plates were then washed serially with PBST buffer before adding 100 µl of 1:50 patient sera in PBS. Plates were then incubated at 37 °C for 1 h before being washed three times with washing buffer and before the addition of 100 µl of 1:5000 anti-human IgG-HRP conjugated antibody. Plates were then incubated at 37 °C for 1 h and washed, and 50 µl of TMB substrate was applied and incubated for 10 min before being stopped with 50 µl of 1 M H 2 SO 4 . The absorbance was measured at 450 nm.

Immunoelectron microscopy
Immunoelectron microscopy (IEM) was carried out as previously described (Utomo et al. 2020) with modifications. The purified antigen sample was added to the Cu-grid transmission electron microscopy (TEM) (Nisshin EM Co., Ltd., Tokyo) and incubated for 30 s at room temperature, washed with 30 µl of PBS, and incubated for 30 s, repeated three times. BSA (30 µl of 2% v/v) was used for blocking after adding a purified antigen sample and washed three times with PBS. The Cu-grid was washed in stages. The first and secondary antibodies were anti-E rabbit polyclonal antibody (FUJIFILM Wako Pure Chemical) diluted 30 times, and goat anti-rabbit IgGconjugated (FUJIFILM Wako Pure Chemical) gold nanoparticles diluted 50 times, respectively. The Cu grid was treated with 1% phosphotungstic acid and analyzed with a JEM-2100F TEM system (JEOL Ltd., Tokyo, Japan).

Mice immunization
Mouse immunization was carried out as previously described (Utomo et al. 2020) with modifications. In this study, 50 BALB/c mice (PT Indoanilab, Bogor, Indonesia) aged 4-6 weeks were divided into ten groups: (i) negative control (PBS), (ii) immunized with alhydrogel as an adjuvant, (iii) immunized with 1CprME, (iv) immunized with 1CprME + adjuvant, (v) immunized with 1prME, (vi) immunized with 1prME + adjuvant, (vii) immunized with 4CprME, (viii) immunized with 4CprME + adjuvant, (ix) immunized with 4prME, and (x) immunized with 4prME + adjuvant. All mice were kept in a temperature-controlled, light-cycled room and were divided into ten groups based on the immunogen. Each mouse was immunized three times intraperitoneally within 2 weeks with 50 μg of purified 1CprME, 1prME, 4CprME, and 4prME proteins with alhydrogel adjuvant. Blood samples were collected via the tail vein on Days 0, 16, and 30, and sera were isolated and stored at -80 °C. All animal procedures were conducted in compliance with established guidelines from the Animal Laboratory of Center of Pharmaceutical and Medical Technology, National Research and Innovation Agency, Indonesia. Animal experiment protocols were reviewed and approved by the Health Research Ethics Committee-University of Indonesia and Cipto Mangunkusumo Hospital (HREC-FMUI/CMH) (approval no. KET-721/UN2.F1/ETIK/PPM.00.02/2021). The interaction between antigens, 1CprME, 1prME, 4CprME, and 4prME, with the respective mice sera, was detected using a direct ELISA method.
One hundred µl of 20 ng/ml diluted antigen, respectively, in coating buffer (0.05 M carbonate-bicarbonate, pH 9.6), was applied to a 96-well ELISA plate and incubated overnight at 4 °C. After incubation, the coating solution was discarded, and a 100 µl blocking solution (5% skim milk in PBS) was added to each well, followed by 1 h at 37 °C incubation. The plates were then washed serially with PBST buffer before adding 100 µl of 1:10 mice sera in PBS. Plates were then incubated at 37 °C for 1 h before being washed three times with washing buffer and before the addition of 100 µl of 1:5000 anti-mouse IgG-HRP conjugated antibody. Plates were then incubated at 37 °C for 1 h and washed, and 50 µl of TMB substrate was applied and incubated for 10 min before being stopped with 50 µl of 1 M H 2 SO 4 . The absorbance was measured at 450 nm.

Results
Expression of 1CprME, 1prME, 4CprME and 4prME polypeptides in silkworm DENV structural proteins are composed of a C, and two membrane proteins, prM and E translated at the beginning of the polyprotein in the order C-prM-E. BmNPV/1CprME (Fig. 1a), BmNPV/1prME (Fig. 1b), BmNPV/4CprME (Fig. 1c), and BmNPV/4prME (Fig. 1d) bacmids were injected into silkworm larvae, and the silkworm hemolymph was collected at 5 dpi. The expression of 1CprME, 1prME, 4CprME, and 4prME in hemolymph samples was confirmed, with molecular weights of 55 kDa at the E protein (Additional file 1: Fig. S1), which corresponded to the estimated weight.
Purification of 1CprME, 1prME, 4CprME and 4prME polypeptides The 1CprME, 1prME, 4CprME, and 4prME polypeptides were purified by affinity chromatography and confirmed by western blot using mouse anti-HA tag antibody for DENV-1 constructs (Fig. 2a, b) and anti-strap tag II antibody for DENV-4 constructs, which showed bands of size 55 kDa at elution fractions (Fr), respectively. To determine whether the purified 1CprME, 1prME, 4CprME, and 4prME polypeptides contained E proteins, western blotting was performed using serotypespecific monoclonal anti-envelope antibodies, an anti-E DENV-1 E29 clone for DENV-1 constructs, and an anti-E DENV-4 E42 clone for DENV-4 constructs. All of the constructs' bands were confirmed to be approximately 55 kDa (Fig. 2e, f ). These results demonstrate that the E proteins were present in the purified 1CprME, 1prME, 4CprME, and 4prME polypeptides. The C protein was confirmed using anti-capsid pAb, which showed a band of size 14 kDa only in CprME constructs (Fig. 2g). Anti-E-DENV-1 E29 clone, anti-E-DENV-2 3H5-1 clone, anti-E-DENV-3 E1 clone, and anti-E-DENV-4 E42 clone antibodies were used to investigate the cross-reactivity of all purified proteins. Specific bands for 1CprME (Fig. 3a), 1prME (Fig. 3b), 4CprME (Fig. 3c), and 4prME (Fig. 3d) could not be detected using the specific serotype antibodies. These results indicate no cross-reactivity between specific serotype antibodies and all the constructs.
Morphology of 1CprME, 1prME, 4CprME and 4prME polypeptides IEM was used to confirm the morphology of the polypeptides 1CprME, 1prME, 4CprME, and 4prME. Spherical structures with sizes ranging from 30 to 55 nm were observed ( Fig. 4a-d), supported by data from dynamic light scattering (Fig. 4e-h). The IEM observation revealed that the particles were lipid bilayer-structured spherical, with some immunogold bound to their surface. The presence of anti-dengue E protein in gold nanoparticles bound to the surface of spherical structures indicates that the particles contain dengue E protein on the surface of the VLPs. According to these results, the 1CprME, 1prME, 4CprME, and 4prME polypeptides expressed in silkworms can generate VLPs of Dengue-1 and -4 (DENV-LPs/1CprME, DENV-LPs/1prME, DENV-LPs/4CprME, and DENV-LPs/4prME).
Heparin-binding assay of the DENV-LPs/1CprME, /1prME, /4CprME, and /4prME A heparin-binding assay was performed to confirm the expression of EDIII on the surface of DENV-LPs. The binding assay of the purified DENV-LPs/1CprME, /1prME, /4CprME, and /4prME was performed using heparin-immobilized microtiter plates. In ELISA, the absorbance increased proportionally to the presence of E (Fig. 5a). These results indicate that the EDIII domain is present on the surface of the DENV-LPs/1CprME, /1prME, /4CprME, and /4prME.

Human DENV-infected sera interaction with DENV-LPs
Purified DENV-LPs/1CprME, /1prME, /4CprME, and /4prME were characterized for their antigenicity toward the patient sera by direct ELISA. As shown in ELISA analysis, DENV-LPs/1CprME, /1prME, /4CprME, and /4prME showed reactivity to patient sera compared to PBS and the rabbit anti-DENV E polyclonal antibody as a positive control (Fig. 6a). DENV-LPs/1CprME, /1prME, /4CprME, and /4prME to patient sera showed significantly high responses compared to anti-E antibody. The Fig. 1 Construction of recombinant dengue virus structural proteins expressed in this study. a 1CprME, b 1prME, c 4CprME, and d 4prME polypeptides of DENV-1 and 4 were expressed in silkworms as a fusion protein with HA + FLAG tags for DENV-1 and Strep-tag II + FLAG tags for  Welch t-test showed a significant difference (p < 0.001) between DENV-LPs-patient sera reactivity to DENV-LPs-positive control or PBS.

Discussion
Previously, DENV-LP/2 has expressed in silkworm larval hemolymph, and DENV-LP/3 was expressed in silkworm larval fat bodies by removing capsid-anchor in the capsid region (Utomo et al. 2019(Utomo et al. , 2020. However, the expressed 1CprME, 1prME, 4CprME, and 4prME polypeptides were detected in hemolymph by adding anchor c to the capsid region. The interaction between heparin and DENV-LPs has been analyzed using multiple assays, including ELISA with immobilized heparin and ITC. Heparin binds to DENV-LPs with K D values of 197-952 nM and ΔG values  Fig. 2 Western blot of purified (a) 1CprME, (b) 1prME, (c) 4CprME and (d) 4prME protein fractions (Fr). Each protein was purified from silkworm hemolymph using anti-FLAG tag protein purification gel column chromatography. E protein was verified using specific serotype monoclonal antibodies using (e) an anti-E E29 clone for DENV-1 constructs and (f) an anti-E E42 clone for DENV-4 antibodies. The C protein also confirmed using anti-capsid pAb (g) from -8.8 to -9.3 kcal mol -1 using the ITC system. According to other references, Marks et al. (2001) used O-sulfated heparin or N-and O-sulfated heparin to bind to the DENV-2 envelope protein expressed in E. coli and analyzed using SPR, yielding a K D of 5 nM. Chen et al. (1997) used heparin to study the binding to the DENV-2 envelope protein expressed on COS-7 mammalian cells. They determined the K D to be 15 nM using ITC. Kim et al. (2017) used heparin to analyze the binding of the ZIKV envelope protein expressed in E. coli and determined the K D to be 433 nM using SPR (Table 2). Compared to a protein subunit, VLPs are complex molecules composed of several protein subunits. It is known that the affinity of the ligand-protein is based on the surface's interaction, leading to the conjugation within the pocket of the protein. Hence, according to the structure of the VLP, it is considered a relatively high molar mass of macromolecules which affects the equilibrium and kinetics of its protein function. Consequently, the low effective molar concentration of a VLP results in the low surface available for binding and the overall affinity of a VLP binding being underestimated. Regarding antiviral activity, sulfated heparin has a better binding ability than heparin. Therefore, sulfated heparin is used to inhibit viral infection of cells. However, unmodified heparin in the cell membrane binds and interacts with EDIII, the putative receptor-binding domain in the flavivirus E protein crystal structure (Frei et al. 2018;Han et al. 2018;Yang et al. 2016;Zautner et al. 2006). EDIII also contains epitopes that block viral adsorption and are targeted by many antibodies, including serotype-specific neutralizing monoclonal antibodies. The conformational flexibility of heparin might permit this molecule to more easily adopt a productive conformation for interaction with the envelope protein. Although it has only a moderate binding affinity, the envelope of DENV-LP is still recognized by heparin on the surface of the cell (Hyatt et al. 2020;Marks et al. 2001). While mammalian cells secrete proteins with correct conformations and full biological activity, insect cells offer advantages compared to those of mammalian cells compared to E. coli or yeast expression systems. The ability to introduce foreign DNA into these cells facilitates a better understanding of the transcriptional, translational, and posttranslational machinery in mammalian cells (Gray 2001;Ikonomou et al. 2003).
The antigens of 1CprME, 1prME, 4CprME, and 4prME also showed reactivity to patient sera high affinity in the direct ELISA. Mixed sera of dengue patients can react to many types of nonspecific DENV epitopes. The strongly correlated reactivities of patient sera with DENV-LPs indicated that the same epitope(s) were displayed on these DENV-LPs. However, there will be a marked difference in the level of antibody reactivity. In other words, the epitope(s) displayed on the DENV-LP surface is comparable with those of the native dengue virus (Danko et al. 2018;Wang et al. 2003).
DENV-LPs/1CprME, /1prME, /4CprME, and /4prME could generate IgG antibody levels since many VLPs include structural or molecular characteristics that give certain auto-immunostimulatory qualities. These features enable VLPs to induce immunological responses without adjuvants. Nevertheless, adjuvants may enhance vaccination immunogenicity and encourage activating a specific type of immune response when combined with VLP vaccines (Cimica and Galarza 2017;Donaldson et al. 2018;Müller et al. 2020). Our ITC data indicate that DENV-LP/1CprME and DENV-LPs/4CprME have a lower K D than DENV-LP/1prME and DENV-LPs/4prME. This demonstrates that the CprME constructs have a higher affinity binding than the prME constructs. Those reactions can be harnessed to perform work inside the body. The IgG elicitation in mice confirmed DENV-LP/ CprMEs elicit a stronger immune response than DENV-LPs/prMEs, which indicates CprME can easily bind to a heparin-like receptor on the surface of the cells compared to prME. This is supported by the results on heparin-binding assays, as the CprME has 4 times lower K D value than prME. This also indicates that the EDIII might be displayed well on the envelope region of the DENV-LP/CprMEs, so it can provide better activity in provoking an immune response in mice.