Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology

Abstract Objective Immunoassay usually deal with the antibody labeling with various reporter molecules, one such useful reporter molecule is horseradish peroxidase (HRPO). Conjugating enzyme with antibody without losing its enzymatic activity is a challenging task. Our aim is to modify existing clas...

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التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Saikant Regidi, Shilpa Ravindran, Ashitha L. Vijayan, Vani Maya, Lakshmi Sreedharan, Jeslin Varghese, Kartik Ramaswami, Manoj Gopi
التنسيق: مقال
اللغة:English
منشور في: BMC 2018-08-01
سلاسل:BMC Research Notes
الموضوعات:
الوصول للمادة أونلاين:http://link.springer.com/article/10.1186/s13104-018-3688-8
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author Saikant Regidi
Shilpa Ravindran
Ashitha L. Vijayan
Vani Maya
Lakshmi Sreedharan
Jeslin Varghese
Kartik Ramaswami
Manoj Gopi
author_facet Saikant Regidi
Shilpa Ravindran
Ashitha L. Vijayan
Vani Maya
Lakshmi Sreedharan
Jeslin Varghese
Kartik Ramaswami
Manoj Gopi
author_sort Saikant Regidi
collection DOAJ
description Abstract Objective Immunoassay usually deal with the antibody labeling with various reporter molecules, one such useful reporter molecule is horseradish peroxidase (HRPO). Conjugating enzyme with antibody without losing its enzymatic activity is a challenging task. Our aim is to modify existing classical method of conjugating antibodies with HRP to enhance immunoassay techniques with better sensitivity. We used chemicals such as sodium meta periodate to generate aldehyde group by oxidation of carbohydrate moieties on HRPO. The activated form of HRPO is lyophilized and then mixed with 1 mg/ml concentration of antibodies to be conjugate. Results After confirming chemical modification of conjugates via UV-Spec and SDS-PAGE independent molecules were used for conjugation and HRP–antibody conjugate. Finally, enzymatic activity of HRP–antibody conjugate was confirmed by performing direct ELISA. Functional properties were analyzed using ELISA with dilution of 1:5000, whereas the conjugate prepared by existing method of conjugation worked with as low dilution of 1:25 with a p value highly significant (< 0.001) for classical verses modified method of conjugation preparation. Collectively, this study showed the enhanced ability of antibody to bind more number of HRPO with an additional step of lyophilization in the regular conjugation protocol. Future exploration are necessary on wide range of IgG antibodies.
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spelling doaj.art-fad750622a944855a901b39f80a5bb5e2022-12-21T18:13:58ZengBMCBMC Research Notes1756-05002018-08-011111610.1186/s13104-018-3688-8Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technologySaikant Regidi0Shilpa Ravindran1Ashitha L. Vijayan2Vani Maya3Lakshmi Sreedharan4Jeslin Varghese5Kartik Ramaswami6Manoj Gopi7Diagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedDiagnostic Products Division & Cell Culture Facility, Corporate R&D Division, HLL Lifecare LimitedAbstract Objective Immunoassay usually deal with the antibody labeling with various reporter molecules, one such useful reporter molecule is horseradish peroxidase (HRPO). Conjugating enzyme with antibody without losing its enzymatic activity is a challenging task. Our aim is to modify existing classical method of conjugating antibodies with HRP to enhance immunoassay techniques with better sensitivity. We used chemicals such as sodium meta periodate to generate aldehyde group by oxidation of carbohydrate moieties on HRPO. The activated form of HRPO is lyophilized and then mixed with 1 mg/ml concentration of antibodies to be conjugate. Results After confirming chemical modification of conjugates via UV-Spec and SDS-PAGE independent molecules were used for conjugation and HRP–antibody conjugate. Finally, enzymatic activity of HRP–antibody conjugate was confirmed by performing direct ELISA. Functional properties were analyzed using ELISA with dilution of 1:5000, whereas the conjugate prepared by existing method of conjugation worked with as low dilution of 1:25 with a p value highly significant (< 0.001) for classical verses modified method of conjugation preparation. Collectively, this study showed the enhanced ability of antibody to bind more number of HRPO with an additional step of lyophilization in the regular conjugation protocol. Future exploration are necessary on wide range of IgG antibodies.http://link.springer.com/article/10.1186/s13104-018-3688-8ConjugationHorseradish peroxidaseELISAImmunoassay
spellingShingle Saikant Regidi
Shilpa Ravindran
Ashitha L. Vijayan
Vani Maya
Lakshmi Sreedharan
Jeslin Varghese
Kartik Ramaswami
Manoj Gopi
Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology
BMC Research Notes
Conjugation
Horseradish peroxidase
ELISA
Immunoassay
title Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology
title_full Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology
title_fullStr Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology
title_full_unstemmed Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology
title_short Effect of lyophilization on HRP–antibody conjugation: an enhanced antibody labeling technology
title_sort effect of lyophilization on hrp antibody conjugation an enhanced antibody labeling technology
topic Conjugation
Horseradish peroxidase
ELISA
Immunoassay
url http://link.springer.com/article/10.1186/s13104-018-3688-8
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