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Biomedical Research

An International Journal of Medical Sciences

Special Issue Article - Biomedical Research (2018) Medical Diagnosis and Study of Biomedical Imaging Systems and Applications

The effect of ultra-high pressure and heat on the allergenicity and structural properties of bovine serum albumin

Yepei Zhu, Wei Wang*, Tianhao Chen and Guanghong Zhou

National Center of Meat Quality and Safety Control, Key Laboratory of Animal Products Processing, Ministry of Agriculture, Synergetic Innovation Center of Food Safety and Nutrition, Nanjing Agricultural University, PR China

*Corresponding Author:
Wei Wang
College of Food Science and Technology
Nanjing Agricultural University, PR China

Accepted on May 22, 2017

DOI: 10.4066/biomedicalresearch.29-16-2065

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The objective of this study is to investigate the impact of Ultra-High Pressure (UHP) combined with moderate heat treatment on the allergenic properties of Bovine Serum Albumin (BSA). The effects of high pressure treatment at 100-500 MPa on allergenicity and structural properties of BSA were investigated. This study was performed using Competitive Indirect-Enzyme Linked Immunosorbent Analysis (CI-ELISA) to get the allergenicity change of BSA and the spectroscopy technology to get the structural properties change. At 500 MPa and 55°C, the inhibition of IgE decreased and reached a maximum of 17.5% relative to untreated BSA. At 100-500 MPa and 25-40°C, the free Sulfhydryl (SH) content, relative surface hydrophobicity (H0) and the fluorescence intensity of BSA significantly (P<0.05) increased at first and then decreased with increasing pressure. A pressure of 100 MPa gave the maximum increase, but using 55°C resulted in a significantly decrease in SH, H0 and fluorescence intensity. This might be due to protein refolding and subsequent aggregation or association. A significant change in the secondary structure was also detected at higher temperatures. UHP combined with higher temperature treatments resulted in a significant decrease in the number of α-helices and a significant increase in β-sheets, β-turns and random coils. These interactions and the secondary results provide direct explanation for the UHP- and heat-induced modification of BSA. This could alter the allergenicity of BSA and enhance the security of beef, milk and beef products.


Ultra-high pressure (UHP), Heat treatment, Bovine serum albumin (BSA), Allergenicity, Structural properties.


Food allergies have become increasingly widespread in recent years and are an important public health concern [1]. Approximately 1-2% of infants, 8% of children, and many adults have some types of food allergy [2,3]. Common examples include wheat, milk, eggs and meat. While avoiding these foods is the most obvious and simple approach to combatting food allergies, these foods are often nutritious and indispensable for normal growth and development. Strict avoidance of food allergens can thus trigger other health issues [4].

Meat and meat products are particularly important foods because of their high nutritional value and functional properties. Although relatively rare compared to common food allergies (e.g., dairy, shrimp, peanuts, etc.), allergies to meat can be very serious and life-threatening [1]. Porcine Serum Albumin (PSA) is one of the man allergens in pork. Many researchers discovered the IgG binding ability of PSA can be reduced to 29% by autoclave treatment at 121 for 30 min [5,6]. Bovine Serum Albumin (BSA) is one of the most important allergens in bovine meat as well as in milk. However, the researches about the BSA allergenicity reduce were rare. Restani et al. [7] suggested that serum albumin antigenicity was only partially correlated with its native three-dimensional structure [8]. Beef allergies often have high cross-reactivity with other meat allergies, and reducing the allergenicity of BSA is very important for beef and cow’s milk [1].

Food technology aims to reduce or eliminate allergenicity by either irreversible removal of allergens or modifying the allergen structure in such a way that the allergenic epitopes are no longer recognized by the immune system. For example, Besler et al. [9] have eliminated allergenic elements from cow’s milk by combining enzymatic and heat treatments with ultra-filtration. In addition, Nishio et al. [10] removed the 16 kDa allergenic components in rice by enzymatic treatment. These hypoallergenic milk and rice products are now supplied to allergic patients. Although enzymatic treatments have generally been used to eliminate food allergenicity, such treatments can also degrade flavor and taste. Moreover, enzymatic treatment of foods with high protein content, e.g. meat, is impractical [1].

Recently, many studies have used Ultra-High Pressure (UHP) to reduce food allergens. This is a non-thermal technology and thus only has a minor influence on small molecule nutrients (amino acids, small molecular components, vitamins, etc.) However, UHP does have significant impact on the secondary, tertiary and quaternary structure of treated protein and thus can markedly alter antigenic properties by modulating noncovalent bonds, hydrogen bonds and hydrophilic interactions [11,12]. Johnson et al. [13] stated that UHP changed the secondary structure of the apple allergens Mal d 1 and Mal d 3 and decreased the immunoreactivity of Mal d 3. Hajos et al. [14] reported that the high pressure caused conformational changes in pork proteins and altered some epitopes. This group found that 600 MPa reduced the IgE immunoreactivity of the proteins in fermented sausage. Therefore, the application of UHP in terms of reducing BSA allergenicity presented great potential.

To the best of our knowledge, less report is conducted to characterize the impact of UHP and moderate heat treatment on the allergenicity of BSA. It was hypothesized that the altered structure of the allergens induced by UHP would have less available to antibody receptors. The objective of this study is to investigate the impact of UHP and different temperatures on the allergenicity of BSA. And the structural properties of BSA including free sulfhydryl content, surface hydrophobicity, extrinsic emission fluorescence spectra and secondary structure were determined. The findings may have important implications both for allergy sufferers and for the food processing community.

Materials and Methods

Antigen and antibodies

BSA and goat anti-mouse IgG conjugated with Horseradish Peroxidase (HRP) were purchased from Sigma Chemical Co. (St Louis, MO, USA). Anti-BSA mouse monoclonal-IgG was provided by National Center of Meat Quality and Safety Control (Nanjing, China).

UHP treatment

A high-pressure chamber (model S-FL-850-9-W; maximum pressure 900 MPa; Stansted Fluid Power, Stansted, UK) with a volume of 300 ml (37 mm in diameter and 300 mm in height). The temperature of the pressure vessel was controlled via circulating water in a cooling jacket. Prior to pressure processing, BSA solutions were vacuum-conditioned in polyethylene bags. Water was used as the pressure-transmitting medium, and its temperature was separately stabilized at the required temperature (25, 40, and 55°C) during pressure processing. BSA was dissolved in 20 mM Tris-HCl (pH 7.0) and was 5% (w/v) in the polyethylene bags. These were pressurized to 100, 300, and 500 MPa for 10 min. After UHP treatment, the BSA solution was removed from the vessel and immediately cooled in an ice bath. Unpressurised samples served as the experimental control group.

Competitive indirect-enzyme linked immunosorbent analysis (CI-ELISA)

Each well was coated with 100 μL of 0.25 μ of BSA solution in a 0.2 M bicarbonate buffer (pH 9.6) at 4°C, overnight. The well was then blocked with 1% gelatin in 0.01 M Phosphate Buffered Saline (PBS) (pH 7.4) for 2 h at 37°C. Next, 50 μL of diluted anti-BSA mouse monoclonal-IgG (1:32000) in 0.01 M PBS and 50 μL of UHP-treated BSA solution (50 were added into each well followed by incubation for 2 h at 37°C. Then, 100 μL of goat anti-mouse IgG conjugated with HRP (1:10000) was added into the well followed by 2 h of incubation at 37°C. Next, 100 μL of freshly prepared 3, 3’, 5, 5’-Tetramethylbenzidine (TMB) substrate was added to each well and reacted for 15 min at 37°C in the dark. The reaction was stopped with 50 μL of 2 M H2SO4. Absorbance was measured at 450 nm using a microplate reader (iMark, Bio-Rad, Hercules, CA, USA). After incubation, the wells were washed three times with 0.01 M PBS containing 0.1% (w/v) Tween 20. All experiments were performed in at least triplicate. The percent inhibition of each test sample was determined using the mean of the experimental wells versus the mean of the control wells using the following formula:


(1) Determination of free sulfhydryl (SH) content

Determination of SH used a modified Ellman’s method and 5, 5’-dithiobis-2-nitrobenzoic acid (DTNB) [15]. The samples were diluted with 20 mM Tris-HCl buffer (pH 7.0) to reach 2.5 of BSA. For the assay, 40 μL of 10 mM DTNB solution (in 0.09 M Gly, 0.004 M EDTA, 0.086 M Tris-HCl buffer, pH 8.0) was added into 4 ml of the sample and reacted for 5 min at 25°C. The absorbance of the mixture was measured at 412 nm using a microplate reader (SpectraMax M2, Molecular Devices Limited, USA) using the buffer as the blank. The SH content was determined by dividing the absorbance by the molar extinction coefficient of 13,600. Each sample was measured in triplicate.

Surface hydrophobicity (H0) determination

The H0 of BSA was determined according to the method of Wang et al. [16], using 1-anilinonaphthalene-8-sulphonic acid (ANS) as the fluorescence probe. Protein dispersions were diluted (0.005-0.2% w/v) in 20 mM Tris-HCl buffer (pH 7.0). Then, aliquots (20 μL) of ANS (8.0 mM in the same buffer) were added to 4 ml of sample. Fluorescence intensity was measured with a microplate reader (SpectraMax M2, Molecular Devices Limited, USA) at wavelengths of 390 nm (excitation) and 470 nm (emission). The initial slope of the fluorescence intensity versus protein concentration was used as an index of H0. Measurements were performed in triplicate.

Extrinsic emission fluorescence spectroscopy

The extrinsic emission fluorescence spectra of BSA were determined according to Wang et al. [16], using 1- anilinonaphthalene-8-sulphonic acid (ANS) as the fluorescence probe in a microplate reader (SpectraMax M2, Molecular Devices Limited, USA). Protein dispersions (0.2 were prepared in 20 mM Tris-HCl (pH 7.0). The samples were excited at 390 nm, and emission spectra were recorded from 420 to 650 nm at a constant slit of 10 nm for both excitation and emission. Measurements were performed in triplicate.

Circular dichroism (CD) spectra determination

Far-UV CD spectra were acquired using a Chirascan spectrophotometer (Applied Photophysics Ltd, Surrey, UK) at room temperature (20 ± 1°C) under a constant flow of nitrogen gas. The 0.5 ml of 0.05 UHP-treated BSA or native BSA in 20 mM Tris-HCl (pH 7.0) was heated to room temperature prior to analysis. Each sample was scanned from 180 to 260 nm. The CD spectrum was obtained as the average of three scans with the 20 mM Tris-HCl background subtracted. Protein secondary structure of the CD spectra (190-260 nm) was analysed by using CDNN 4.1. All measurements were performed in triplicate.

Statistical analysis

All experiments were performed in triplicate, and data were evaluated with a one-way Analysis of Variance (ANOVA) using SPSS Version 9.0 program (SPSS, Chicago, IL, USA). Statistical differences with P-values under 0.05 were considered to be significant.

Results and Discussion

Effect of UHP and heat treatment on the allergenicity of BSA

Table 1 shows the effects of UHP and temperature on the allergenicity of BSA. The UHP treatment at various temperatures reduced allergenicity of UHP-treated BSA relative to the control sample. At 100 MPa and 25°C, no significant inhibition effect was observed. The 500 MPa and 55°C, however, gave the lowest inhibition of 17.53. The inhibition of 500 MPa and 55°C was 1/6 of the control.

Treatment 25°C 40°C 55°C
Control 100.00 ± 0.01a 95.42 ± 0.89a 90.11 ± 0.72a
100 MPa 97.14 ± 0.03a 92.55 ± 0.97b 80.21 ± 1.49c
300 MPa 90.71 ± 0.05b 75.78 ± 0.67d 42.42 ± 1.46e
500 MPa 83.37 ± 0.09c 51.21 ± 1.81f 17.53 ± 2.08g

Table 1. Effects of UHP and heat treatment on BSA allergenicity (SD, n=3).

The CI-ELISA assessed the immunochemical reactivity in untreated and UHP-treated BSA. The data indicated that UHP combined with heat treatment led to a greater reduction in allergenicity of BSA. Han et al. [17] suggested that high pressure treatments(200 MPa-600 MPa) or the treatment on BGG do not show any significant changes in the allergenicity of BGG. The results might suggest BGG is heat and high pressure resistant which is different with BSA. BSA is more heat -sensitive than BGG [18]. So the treatment of HHP combined with moderate temperature on BSA gave a better allergenicity reduce as our results showed.

The decreased allergenicity of BSA might be attributed to protein conformation changes caused by high pressure and moderate temperature. It is known that UHP can induce structural unfolding, precipitation, protein denaturation, and even dissociation of some proteins into subunits. Conformational changes such as protein refolding or reaggregation may actually hide some conformational epitopes or IgE binding sites so that some allergen activities could be minimized [19].

A similar phenomenon has been reported by Nogami et al. [20] who showed that the high pressure treatment of BSA at 300-600 MPa could efficiently reduce histamine release from cells. This indicated that pressure could reduce the allergenicity of BSA-containing foods.

Ultra high pressure and heat treatment on tertiary structure of BSA

The free SH content of BSA samples was significantly influenced by UHP treatment pressure and temperature (Table 2). From 25-40°C, the free SH content of BSA first increased and then decreased with pressure increases; 100 MPa produced the highest increase, which was 4.82 μmol/g protein. However, as the temperature increased to 55°C, the free SH content significantly (P<0.05) decreased to. At the same pressure, the free SH content in BSA significantly (P<0.05) decreased as the temperature was raised from 25°C to 55°C (Table 2).

Treatment Free sulfhydryl content of BSA (μmol/g protein)
25°C 40°C 55°C
Control 3.32 ± 0.05a  3.95 ± 0.09a 3.34 ± 0.05a
100 MPa 4.82 ± 0.03e 4.14 ± 0.03b 3.16 ± 0.02d
300 MPa 4.22 ± 0.06b 3.39 ± 0.05c 2.60 ± 0.03f
500 MPa 3.23 ± 0.06d 2.67 ± 0.02f 2.18 ± 0.04g

Table 2. Effects of UHP and heat treatment on free sulfhydryl content of BSA (Treatment time is fixed at 10 min).

The use of 100 MPa and 25°C to 40°C heating offered the highest free SH values. Similar results were reported by Wei et al. [21] who found that the value of SH in egg yolk increased and then decreased with the highest values at 300 MPa. There are 17 disulfide bonds and a free-SH group in BSA [22]. The increase of SH content might suggest that a disruption of the disulfide bond within the protein. Meanwhile, unfolding the protein could expose the sulfhydryl groups buried in the interior of the protein, leading to an increase in the free SH content [23,24]. At this pressure, the free SH groups are stable with relatively little aggregation. At higher pressure and temperatures, hydrophobic interactions or sulfhydryl-disulfide exchange led to the aggregation/reaggregation of unfolded proteins [20].

However, the impact of modulating disulfide bonds is critical [22]. Restani et al. [22] showed that conservation of disulfide bridges is a critical factor in maintaining BSA antigenicity. These loops are critical in the maintenance of the conformational epitopes of BSA. Therefore, UHP affects the free SH content and interferes with the structure of the BSA epitopes to reduce allergicity [25].

The BSA H0 data is shown in Table 3. From 25°C to 40°C, the H0 of BSA increased greatly (P<0.05) at 100 MPa relative to control. It decreased from 300 to 500 MPa. When the temperature was 55°C, however, the H0 decreased from 69.79 to 19.68 at the pressure range of 100 to 500 MPa.

Treatment Relative surface hydrophobicity (H0)
25°C 40°C 55°C
Control 100.00 ± 1.75b  98.81 ± 1.29a  96.53 ± 0.22a
100 MPa 109.30 ± 1.20a 108.30 ± 1.50c 69.79 ± 2.58d
300 MPa 95.72 ± 1.21a 58.96 ± 0.78e 35.19 ± 1.10g
500 MPa 71.19 ± 2.06d 20.66 ± 0.66f 19.68 ± 0.40g

Table 3. Effects of UHP and heat treatment on the relative surface hydrophobicity of BSA.

The H0 data reflect differences in protein aggregation or refolding. UHP may cause the hydrophobic groups that were buried in the hydrophobic interior to become exposed to the solvent. This will disrupt the hydrogen bonds that modulate protein folding. Thus, the H0 of BSA increased from 25-40°C at 100 MPa relative to controls [12]. The UHP (300 and 500 MPa) and a higher temperature (55°C), however; decreased the H0. The UHP and heating may cause association of subunits and disrupt the tertiary structure. It may result in aggregation. Thus, the decrease in surface hydrophobicity of BSA after pressure and moderate heating was probably related to the formation of soluble and insoluble aggregates of subunits. Thus, it is possible that the treatments lead to intense proteinprotein interactions via the formation of complex aggregates caused by reduced exposure of the hydrophobic groups [12,21].

Table 4 shows the fluorescence intensity of ANS binding to BSA treated at various pressures and temperatures. The fluorescence emission intensity indicated a gradual decrease at 100, 300, and 500 MPa. The fluorescence intensity which was positively correlated with surface hydrophobicity was higher than the control induced by a pressure of 100 MPa from 25-40°C. When the temperature increased to 55°C, the value of fluorescence intensity decreased to a minimum compared with the others.

Treatment Emission intensity
25°C 40°C 55°C
Control 2239.92 2029.38 1921.43
100 MPa 4829.98 2879.55 1822.54
300 MPa 3692.96 1801.50 1343.37
500 MPa 2166.12 1414.43 832.13

Table 4. Effects of UHP and heat treatment on the fluorescence emission intensity of BSA.

ANS is fluorescent dye that binds to nonpolar regions of proteins by non-covalent bonds. It offers sensitive detection of structural changes and aggregated protein [26]. These findings agree with Yan et al. [21], who found that a pressure of 100-500 MPa significantly decreased H0; 50°C treatment affected the weak binding site close to the C-terminal. Therefore, the H0 decreased relative to the UHP-treated samples [26,27].

UHP (100 MPa at 25-40°C) can cause the hydrophobic groups buried within the hydrophobic interior to come to the exterior. When treated at a higher pressure and temperature, the fluorescence intensity significantly decreased. A similar phenomenon was reported by Nogami et al. [20], who confirmed that 100 MPa for 10 min at 15°C markedly decreased the fluorescence intensity of BSA.

The decrease in fluorescence indicated a loosening of the protein conformation, which reduced ANS binding and offered increased exposure of the hydrophobic groups [28]. At 500 MPa at 55°C, the fluorescence data indicated that the binding regions of BSA-ANS became more hydrophilic. Thus, the ANS separated from the binding motif-this decreased the fluorescence. On the other hand, Takeda et al. [27] reported that ANS binds to BSA in up to five different binding sites. Thus, heating could disturb the affinity of the weak sites.

Effects of ultra-high pressure and heat treatment on secondary structure of BSA

Table 5 shows far-UV CD data. The result indicated a decrease in the α-helix and an increase in the β-sheet. Meanwhile, the zero-crossing points shifted to the left. The CD spectrum of native BSA is characteristic of 67.9 % α-helix, 3.8 % β-sheet,11.9 % β-turn, and 16.5% random coil. The change in secondary structure of BSA after pressurization and heat treatments are shown in Table 5. The temperature combined and UHP significantly decreased the α-helix and significantly increased the β-sheets, β-turns and random coils. The helical proportion sharply decreased to 37.8% upon raising the temperature to 55°C.

Treatment α-helix (%) β-sheet (%) β-turn (%) Random coil (%)
Control 67.9 ± 1.1a 3.8 ± 0.3d 11.9 ± 0.1g 16.5 ± 0.7e
100 MPa, 25°C 64.2 ± 0.5b 4.4 ± 0.2d 12.4 ± 0.1f 19.0 ± 0.3d
300 MPa, 25°C 54.2 ± 0.9c 6.5 ± 0.4c 14.0 ± 0.2de 25.2 ± 0.4c
500 MPa, 25°C 45.8 ± 1.5d 9.5 ± 0.7b 15.4 ± 0.2bc 29.4 ± 0.6b
Control 63.2 ± 0.2a 4.1 ± 0.3d 12.4 ± 0.1g  20.1 ± 0.9e
100 MPa, 40°C 62.5 ± 1.7b 4.7 ± 0.4d 12.6 ± 0.2f 20.2 ± 1.1d
300 MPa, 40°C 53.7 ± 0.7c 6.7 ± 0.2c 14.2 ± 0.2d 25.5 ± 0.4c
500 MPa, 40°C 44.9 ± 0.8d 10.0 ± 0.4b 15.6 ± 0.2b 29.5 ± 0.3b
Control 60.5 ± 0.9a 5.2 ± 0.3d 13.1 ± 1.9g 21.2 ± 0.3e
100 MPa, 55°C 56.0 ± 0.4c 6.0 ± 0.2c 13.7 ± 0.1e 24.2 ± 0.1c
300 MPa, 55°C 47.4 ± 0.3d 9.4 ± 0.8b 15.0 ± 0.2c 28.3 ± 0.8b
500 MPa, 55°C 37.8 ± 0.3e 14.0 ± 0.4a 16.6 ± 0.1a 31.6 ± 0.2a

Table 5. Effects of UHP and heat treatment on secondary structure composition of BSA (SD, n=3).

The secondary structures include α-helix, β-sheet, β-turn and random coil. The literature suggests that higher temperatures and pressures will seriously denature BSA. In our study, the greatest change was observed for the sample treated for 10 min at 500 MPa and 55°C. Yamamoto et al. [1] treated BSA with 600 MPa at 5-7°C for 5 min. They showed only a slight increase in the β-structure after treatment with no significant change in the secondary structure. They concluded that changing the secondary structure did not reduce allergenicity. In contrast, our results showed that the high pressure and moderate heat treatments induced significant alterations in secondary structures. These alterations of secondary structures suggested that the allergenicity of BSA might be associated with the secondary structure.

Barbara et al. [29] suggested that serum albumin antigenicity was only partially correlated with its native three-dimensional structure. BSA is a heart-shaped protein composed of three structurally similar helical domains termed I-III. Many of the BSA epitopes are located on the α-helices of domain II [30]. Thus, the reduced allergenicity might be that the high temperature and pressure destroyed some secondary structures of BSA.

Discussion and Conclusion

Pressure and heat treatment affect the structure of BSAespecially the tertiary structure. The UHP and heat result in unfolding, aggregation and conformational changes. The free SH content and the H0 increased and then decreased sharply as a function of pressure (300-500 MPa) at 25-40°C which indicated that the conformational changes are due to protein unfolding from broken disulfide bonds. At 55°C, the decreasing value of SH and H0 indicates an impact on sulfhydryl-disulfide exchange. In turn, the reaction of hydrophobic groups increased. Additionally, UHP resulted in a significant decrease in the α-helix, while there was a significant increase in the β-sheet, β-turn and random coil. The treatment could destroy some secondary structures of BSA. This combination of UHP and moderate heat treatments might not only prevent beef and milk allergies, but could also be applied to produce hypoallergenic beef and milk.

Contribution of Authors

Yepei Zhu and Wei Wang have equal contribution to this work.

Conflict of Interest

No conflict of interest associated with this work.


This work was supported by Natural Science Foundation of Jiangsu Province (BK20140722) and the National Natural Science Foundation of the People's Republic of China (31501395).