Molecular and immunological characterization of cysteine protease from Phaseolus vulgaris and evolutionary cross-reactivity
Akansha Sharma
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Department of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, India
Contribution: Conceptualization, Methodology, Writing - original draft, Writing - review & editing
Search for more papers by this authorSrishti Vashisht
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Contribution: Writing - review & editing
Search for more papers by this authorRicha Mishra
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Academy of Scientific and Innovative Research, Ghaziabad, India
Contribution: Writing - review & editing
Search for more papers by this authorShailendra Nath Gaur
Department of Respiratory Medicine, Vallabhbhai Patel Chest Institute, University of Delhi, New Delhi, India
Contribution: Resources, Supervision
Search for more papers by this authorNagendra Prasad
Bengaluru Allergy Centre, Bangalore, India
Contribution: Resources, Supervision
Search for more papers by this authorShakuntala Lavasa
USLavasa Medical & Research Center, Chandigarh, India
Contribution: Resources, Supervision
Search for more papers by this authorJanendra Kumar Batra
Department of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, India
Contribution: Supervision
Search for more papers by this authorCorresponding Author
Naveen Arora
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Correspondence
Naveen Arora, Allergy and Immunology Division, CSIR-Institute of Genomics and Integrative Biology, Delhi University Campus, Room 509, Mall Road, Opposite Jubilee Hall, New Delhi-110007, India.
Email: [email protected]
Contribution: Conceptualization, Funding acquisition, Supervision, Writing - review & editing
Search for more papers by this authorAkansha Sharma
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Department of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, India
Contribution: Conceptualization, Methodology, Writing - original draft, Writing - review & editing
Search for more papers by this authorSrishti Vashisht
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Contribution: Writing - review & editing
Search for more papers by this authorRicha Mishra
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Academy of Scientific and Innovative Research, Ghaziabad, India
Contribution: Writing - review & editing
Search for more papers by this authorShailendra Nath Gaur
Department of Respiratory Medicine, Vallabhbhai Patel Chest Institute, University of Delhi, New Delhi, India
Contribution: Resources, Supervision
Search for more papers by this authorNagendra Prasad
Bengaluru Allergy Centre, Bangalore, India
Contribution: Resources, Supervision
Search for more papers by this authorShakuntala Lavasa
USLavasa Medical & Research Center, Chandigarh, India
Contribution: Resources, Supervision
Search for more papers by this authorJanendra Kumar Batra
Department of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, India
Contribution: Supervision
Search for more papers by this authorCorresponding Author
Naveen Arora
Allergy and Immunology Section, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India
Correspondence
Naveen Arora, Allergy and Immunology Division, CSIR-Institute of Genomics and Integrative Biology, Delhi University Campus, Room 509, Mall Road, Opposite Jubilee Hall, New Delhi-110007, India.
Email: [email protected]
Contribution: Conceptualization, Funding acquisition, Supervision, Writing - review & editing
Search for more papers by this authorAbstract
A commonly consumed legume in India, the kidney bean (Phaseolus vulgaris) is associated with allergy. We report molecular and immunological characterization of cysteine protease allergen and its cross-reactivity. In silico allergenicity assessment and phylogenetic analysis of kidney bean cysteine protease showed significant sequence homology (upto 67%) with allergens from kiwi, papaya, soybean, ragweed pollen and mites. Physicochemical properties and motif-analysis depicted cysteine protease as probable allergen. Multiple sequence alignment and phylogenetic analysis indicated structural conservation between kidney bean and homologous cysteine protease sequences. The gene was cloned, expressed and affinity purified. Cysteine protease was resolved at 42 kDa and exhibited high IgE binding (up to 89%) with hypersensitive sera. Cysteine protease showed functional property on cross-linking IgE receptors and upregulated expression of CD203c on activated basophils. In inhibition studies, 8.4 ng of cysteine protease was required for 50% self-inhibition, whereas significant inhibition was also observed with kidney bean (52 ng), black gram (155 ng), chick pea (437 ng), mesquite pollen (36 ng), house dust mite (64.85 ng), Alternaria alternata (78.8 ng) and Curvularia lunata (73.6 ng) extracts. ConSurf analysis indicated conserved active site and catalytic residues in mature domain among proteases from legumes, fruits, pollens, mites and fungus. In summary, P. vulgaris cysteine protease was molecularly characterized having functional activity. This study demonstrated, cross-reactivity between food and aeroallergens based on evolutionary conservancy that showed its clinical importance as cross-reactive allergen.
Practical applications
Adaptation of sustainable lifestyle has led to a surge in consumption of plant-based foods especially legumes. Their high nutritional content lowers the risk of developing cardiovascular diseases, diabetes, obesity, and stroke. Kidney beans, a commonly consumed legume in Indian subcontinent, have a potential to be used as nutraceutical and functional food. Despite its alimentary nature, it elicits allergic reactions. Being a major sensitizer, trivial information regarding its allergic components has led to an urgent need for exploring its allergen repertoire. Our study reported biochemical and immunological characterization of its major cysteine protease allergen. Cysteine proteases are major cross-reactive allergens from insects, fruits and fungal sources. Identification and molecular characterization of such immunodominant allergens by RDT offers the prospect of using recombinant proteins for accurate diagnosis and therapeutic purposes. This study suggests that a potential major cross-reactive allergen may aid in developing allergy management interventions for a wide range of allergenic sources.
CONFLICT OF INTEREST
The authors declare no conflict of interest.
Supporting Information
Filename | Description |
---|---|
jfbc14232-sup-0001-Supinfo.docxWord 2007 document , 2.7 MB |
Appendix S1 Supporting Information |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
REFERENCES
- Ashkenazy, H., Abadi, S., Martz, E., Chay, O., Mayrose, I., Pupko, T., & Ben-Tal, N. (2016). ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules. Nucleic Acids Research, 44, W344–W350. https://doi.org/10.1093/nar/gkw408
- Arora, B., Sharma, S., Gaur, S. N., Jain, V. K., Lavasa, S., & Arora, N. (2021). Identification of a vicilin-like major allergen from Prosopis juliflora exhibiting cross- reactivity with legume food allergens. Molecular Immunology, 137, 84–93. https://doi.org/10.1016/J.MOLIMM.2021.06.023
- Berezin, C., Glaser, F., Rosenberg, J., Paz, I., Pupko, T., Fariselli, P., Casadio, R., & Ben-Tal, N. (2004). ConSeq: the identification of functionally and structurally important residues in protein sequences. Bioinformatics (Oxford, England), 20(8), 1322–1324. https://doi.org/10.1093/BIOINFORMATICS/BTH070
- Bouley, J., Groeme, R., Le Mignon, M., Jain, K., Chabre, H., Floch, V. B., Couret, M.-N., Bussieres, L., Lautrette, A., Naveau, M., Baron-Bodo, V., Lombardi, V., Mascarell, L., Batard, T., Nony, E., & Moingeon, P. (2015). Identification of the cysteine protease Amb a 11 as a novel major allergen from short ragweed. Journal of Allergy and Clinical Immunology, 136(4), 1055–1064. https://doi.org/10.1016/j.jaci.2015.03.001
- Bublin, M., Maria, K., Christian, R., Christine, H., Zsolt, S., Varga, E. M., Soheila, J. M., Karin, H-S., & Heimo, B. (2013). IgE cross-reactivity between the major peanut allergen ara h 2 and the nonhomologous allergens ara h 1 and ara h 3. Journal of Allergy and Clinical Immunology, 132(1), 118–124. https://doi.org/10.1016/J.JACI.2013.01.022
- Cabanillas, B., Jappe, U., & Novak, N. (2018). Allergy to peanut, soybean, and other legumes: Recent advances in allergen characterization, stability to processing and IgE cross-reactivity. Molecular Nutrition and Food Research, 62(1), 1–40. https://doi.org/10.1002/mnfr.201700446
- Cromwell, O., Häfner, D., & Nandy, A. (2011). Recombinant allergens for specific immunotherapy. Journal of Allergy and Clinical Immunology, 127(4), 865–872. https://doi.org/10.1016/j.jaci.2011.01.047
- Furmonaviciene, R., Sutton, B. J., Glaser, F., Laughton, C. A., Jones, N., Sewell, H. F., & Shakib, F. (2005). An attempt to define allergen-specific molecular surface features: a bioinformatic approach. Bioinformatics, 21(23), 4201–4204. https://doi.org/10.1093/bioinformatics/bti700
- Furmonaviciene, R., Sewell, H. F., & Shakib, F. (2000). Comparative molecular modelling identifies a common putative IgE epitope on cysteine protease allergens of diverse sources. Clinical and Experimental Allergy, 30(9), 1307–1313. https://doi.org/10.1046/j.1365-2222.2000.00897.x
- Gouet, P., Courcelle, E., Stuart, D. I., & Métoz, F. (1999). ESPript: Analysis of multiple sequence alignments in PostScript. Bioinformatics, 15(4), 305–308. https://doi.org/10.1093/bioinformatics/15.4.305
- Govindaraj, D., Swati, S., Gaur, S. N., Lavasa, S., Prasad, N., Arora, N., & Ph, D. (2016). Immunogenic peptides: B & T Cell epitopes of per a 10 allergen of periplaneta Americana. Molecular Immunology, 80, 24–32 https://doi.org/10.1016/j.molimm.2016.10.007
- Groeme, R., Airouche, S., Kopec, D., Jaekel, J., Savko, M., Berjont, N., Bussieres, L., Le Mignon, M., Jagic, F., Zieglmayer, P., Baron-bodo, V., Floch, V. B., Mascarell, L., Briozzo, P., & Moingeon, P. (2016). Structural and functional characterization of the major allergen Amb a 11 from short ragweed pollen *. Journal of Biological Chemistry, 291(25), 13076–13087. https://doi.org/10.1074/jbc.M115.702001
- Guha, K. B., & Gupta, P. (2020). Growing trend of veganism in metropolitan cities: Emphasis on baking.
- He, S., Zhao, J., Elfalleh, W., Jemaà, M., Sun, H., Sun, X., Tang, M., He, Q., Wu, Z., & Lang, F. (2018). In Silico identification and in vitro analysis of B and T-Cell epitopes of the black turtle bean (Phaseolus Vulgaris L.) lectin. Cellular Physiology and Biochemistry, 49(4), 1600–1614 https://doi.org/10.1159/000493496
- He, L., Zhu, J. (2015). Computational tools for epitope vaccine design and evaluation. Current Opinion in Virology, 11, 103-112. https://doi.org/10.1016/j.coviro.2015.03.013
- Jenkins, J. A., Griffiths-Jones, S., Shewry, P. R., Breiteneder, H., & Mills, E. N. C. (2005). Structural relatedness of plant food allergens with specific reference to cross-reactive allergens: An in silico analysis. Journal of Allergy and Clinical Immunology, 115(1), 163–170. https://doi.org/10.1016/j.jaci.2004.10.026
- Jimenez-Lopez, J. C., Robles-Bolivar, P., Lopez-Valverde, F. J., Lima-Cabello, E., Kotchoni, S. O., & Alché, J. D. (2016). Ole e 13 is the unique food allergen in olive: Structure-functional, substrates docking, and molecular allergenicity comparative analysis. Journal of Molecular Graphics and Modelling, 66, 26–40. https://doi.org/10.1016/j.jmgm.2016.03.003
- Kasera, R., Singh, A. B., Lavasa, S., Nagendra, K., & Arora, N. (2013). Purification and immunobiochemical characterization of a 31 kDa cross-reactive allergen from Phaseolus vulgaris (kidney bean). PloS one, 8(5), e63063. https://doi.org/10.1371/journal.pone.0063063
- Kasera, R., Singh, B. P., Lavasa, S., Prasad, K. N., Ramesh, C., & Singh, A. B. (2011). Kidney bean: A major sensitizer among legumes in asthma and rhinitis patients from India. PLoS One, 6(11), e27193. https://doi.org/10.1371/journal.pone.0027193
- Kimothi, S., & Dhaliwal, Y. S. (2020). Nutritional and Health Promoting Attribute of Kidney Beans (Phaseolus vulgaris L.): A Review. International Journal of Current Microbiology and Applied Sciences, 9(5), 1201–1209. https://doi.org/10.20546/IJCMAS.2020.905.134
- Kumar, R., Kumari, D., Srivastava, P., Khare, V., Fakhr, H., Arora, N., Gaur, S. N., & Singh, B. P. (2010). Identification of IgE-mediated food allergy and allergens in older children and adults with asthma and allergic rhinitis. The Indian Journal of Chest Diseases & Allied Sciences, 52(4), 217–224.
- Kumar, R., Singh, B. P., Srivastava, P., Sridhara, S., Arora, N., & Gaur, S. N. (2006). Relevance of serum IgE estimation in allergic bronchial asthma with special reference to food allergy. Asian Pacific Journal of Allergy and Immunology, 24(4), 191–199.
- Kumar, S., Kumar, A., Das, M., Jain, S. K., & Dwivedi, P. D. (2013). Clinical complications of kidney bean (Phaseolus vulgaris L.) consumption. Nutrition, 29(6), 821–827. https://doi.org/10.1016/j.nut.2012.11.010
- Kumar, S., Kumar, A., Sharma, A., Kumar, D., Tripathi, A., Chaudhari, B. P., Das, M., Jain, S. K., & Dwivedi, P. D. (2013). Phytohemagglutinins augment red kidney bean (Phaseolus vulgaris L.) induced allergic manifestations ☆. Journal of Proteomics, 93, 50–64. https://doi.org/10.1016/j.jprot.2013.02.003
- Kumar, S., Kumar, A., Sharma, A., Roy, R., Kumar, D., Bh, G., Tripathi, A., Chaudhari, B. P., Das, M., Jain, S. K., & Dwivedi, P. D. (2014). International Immunopharmacology Phaseolin: A 47. 5 kDa protein of red kidney bean (Phaseolus vulgaris L.) plays a pivotal role in hypersensitivity induction. International Immunopharmacology, 19(1), 178–190. https://doi.org/10.1016/j.intimp.2014.01.014
- Medawar, E., Huhn, S., Villringer, A., & Veronica Witte, A. (2019). The effects of plant-based diets on the body and the brain: A systematic review. Translational Psychiatry, 9(1), 1–17. https://doi.org/10.1038/s41398-019-0552-0
- Mishra, A., Jain, A., & Arora, N. (2015). Mapping B-Cell epitopes of major and minor peanut allergens and identifying residues contributing to IgE binding https://doi.org/10.1002/jsfa.7121.
10.1002/jsfa.7121 Google Scholar
- Mishra, A., Gaur, S. N., Singh, B. P., & Arora, N. (2012). In silico assessment of the potential allergenicity of transgenes used for the development of gm food crops. Food and Chemical Toxicology, 50(5), 1334–1339 https://doi.org/10.1016/j.fct.2012.02.005
- Misra, A., Prasad, R., Das, M., & Dwivedi, P. D. (2008). Prevalence of legume sensitization in patients with naso-bronchial allergy. Immunopharmacology and Immunotoxicology, 30(3), 529–542. https://doi.org/10.1080/08923970802135294
- Nair, S., Kukreja, N., Singh, B. P., & Arora, N. (2011). Identification of B Cell epitopes of alcohol dehydrogenase allergen of curvularia Lunata. PloS One, 6(5) https://doi.org/10.1371/JOURNAL.PONE.0020020
- Nugraha, R., Kamath, S. D., Johnston, E., Karnaneedi, S., Ruethers, T., & Lopata, A. L. (2019). Conservation analysis of B-Cell allergen epitopes to predict clinical cross-reactivity between shellfish and inhalant invertebrate allergens. Frontiers in Immunology, 10(November), 1–13. https://doi.org/10.3389/fimmu.2019.02676
- Oezguen, N., Zhou, B., Negi, S. S., Ivanciuc, O., Schein, C. H., Labesse, G., & Braun, W. (2008). Comprehensive 3D-modeling of allergenic proteins and amino acid composition of potential conformational IgE epitopes. Molecular Immunology, 45(14), 3740 https://doi.org/10.1016/J.MOLIMM.2008.05.026
- Polak, R., Phillips, E. M., & Campbell, A. (2015). Legumes: Health benefits and culinary approaches to increase intake. Clinical Diabetes, 33(4), 198–205. https://doi.org/10.2337/diaclin.33.4.198
- Pomés, A. (2010). Relevant B Cell Epitopes in Allergic Disease. International archives of allergy and immunology, 152(1), 1–11 https://doi.org/10.1159/000260078
- Ramakrishna, V., & Rao, P. R. (2014). Purification of acidic protease from the cotyledons of germinating Indian bean (Dolichos lablab L. var lignosus) seeds. African Journal of Biotechnology, 4(7), 703–707. https://doi.org/10.5897/ajb2005.000-3130
10.5897/ajb2005.000?3130 Google Scholar
- Rougé, P., Culerrier, R., Thibau, F., Didier, A., & Barre, A. (2011). A case of severe anaphylaxis to kidney bean: Phaseolin (vicilin) and PHA (lectin) identified as putative allergens. Allergy: European Journal of Allergy and Clinical Immunology, 66(2), 301–302). John Wiley & Sons Ltd. https://doi.org/10.1111/j.1398-9995.2010.02466.x
- Santos, A. F., James, L. K., Bahnson, H. T., Shamji, M. H., Couto-Francisco, N. C., Islam, S., Houghton, S., Clark, A. T., Stephens, A., Turcanu, V., Durham, S. R., Gould, H. J., & Lack, G. (2015). IgG4 inhibits peanut-induced basophil and mast cell activation in peanut-tolerant children sensitized to peanut major allergens. Journal of Allergy and Clinical Immunology, 135(5), 1249–1256. https://doi.org/10.1016/j.jaci.2015.01.012
- Shamji, M. H., Kappen, J. H., Akdis, M., Jensen-Jarolim, E., Knol, E. F., Kleine-Tebbe, J., Bohle, B., Chaker, A. M., Till, S. J., Valenta, R., Poulsen, L. K., Calderon, M. A., Demoly, P., Pfaar, O., Jacobsen, L., Durham, S. R., Schmidt-Weber, C. B., & Biomarkers, S.-W. C. (2017). Biomarkers for monitoring clinical efficacy of allergen immunotherapy for allergic rhinoconjunctivitis and allergic asthma: An EAACI Position Paper. Allergy, 72(8), 1156–1173. https://doi.org/10.1111/all.13138
- Sircar, G., Saha, B., Mandal, R. S., & Pandey, N. (2015). Purification, cloning and immuno- biochemical characterization of a fungal aspartic protease allergen Rhi o 1 from the airborne mold Rhizopus oryzae. PLoS One, 10(12), e0144547. https://doi.org/10.1371/journal.pone.0144547
- Smits, M., Le, T.-M., Welsing, P., Houben, G., Knulst, A., & Verhoeckx, K. (2018). Legume protein consumption and the prevalence of legume sensitization. Nutrients, 10(10), 1545. https://doi.org/10.3390/nu10101545
- Soeria-Atmadja, D., Önell, A., Kober, A., Matsson, P., Gustafsson, M. G., & Hammerling, U. (2007). Multivariate statistical analysis of large-scale IgE antibody measurements reveals allergen extract relationships in sensitized individuals. Journal of Allergy and Clinical Immunology, 120(6), 1433–1440 https://doi.org/10.1016/J.JACI.2007.07.021
- Takai, T., Kato, T., Sakata, Y., Yasueda, H., Izuhara, K., Okumura, K., & Ogawa, H. (2005). Recombinant Der p 1 and Der f 1 exhibit cysteine protease activity but no serine protease activity. Biochemical and Biophysical Research Communications, 328(4), 944–952. https://doi.org/10.1016/j.bbrc.2005.01.051
- Uberti, F., Peñas, E., Manzoni, Y., di Lorenzo, C., Ballabio, C., Fiocchi, A., Terracciano, L., & Restani, P. (2015). Molecular characterization of allergens in raw and processed kiwifruit. Pediatric Allergy and Immunology, 26(2), 139–144. https://doi.org/10.1111/pai.12345
- Wu, B., Toussaint, G., Vander Elst, L., Granier, C., Jacquemin, M. G., & Saint-Remy, J. M. (2000). Major T Cell epitope-containing peptides can elicit strong antibody responses. European Journal of Immunology, 30(1): 291–299. https://doi.org/10.1002/1521-4141.
- Zheng, L.-n., Lin, H., Pawar, R., Li, Z.-x., & Li, M.-h. (2011). Mapping IgE binding epitopes of major shrimp (penaeus monodon) allergen with immunoinformatics tools. Food and Chemical Toxicology, 49(11), 2954–2960. https://doi.org/10.1016/j.fct.2011.07.043