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Production and evaluation of egg derived hot start antibodies
Author(s) -
V. G. Spyrydonov,
Dmitro Pihida,
Alexander Sereda,
Artur Likhanov,
Weiming Yu
Publication year - 2020
Publication title -
electronic journal of biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.603
H-Index - 57
ISSN - 0717-3458
DOI - 10.1016/j.ejbt.2020.01.005
Subject(s) - hot start pcr , dna polymerase , polyclonal antibodies , microbiology and biotechnology , taq polymerase , polymerase , antibody , multiple displacement amplification , chemistry , polymerase chain reaction , biology , dna , thermus aquaticus , dna extraction , biochemistry , nested polymerase chain reaction , gene , genetics
Background Hot start can greatly improve specificity, sensitivity and yield of PCR. Non-specific amplification can occur in PCR when reaction mixture is prepared at room temperature, because Taq DNA polymerase is active and the primers can hybridize non-specifically. Hot start Taq DNA polymerases remain inactive at room temperature and are activated after heating at 95°C preventing non-specific amplification. Monoclonal antibodies against Taq DNA polymerase is the first line of reagents used for turn on regular Taq DNA polymerase into Hot start one. The goal of this research was to produce and evaluate Hot Start antibodies derived from chicken eggs. Results We performed affinity purification of yolk immunoglobulin (IgY) and obtained polyclonal Hot Start antibodies. The yield of specific antibodies was 0.36 mg per egg or 0.2% of total yolk antibodies. The protocol for real time measurement and Hot start IgY activity assessment was developed. We found that Hot start IgY can reversibly block Taq DNA polymerase activity at 50°C and have no negative impact neither on the Taq DNA polymerase activity after denaturation nor on the reverse transcriptase. We estimated that 1.0 μg of Hot start IgY effectively blocks 5 U activity of Taq DNA polymerase. Conclusions Egg derived Hot Start polyclonal antibodies are the cheapest source of Hot start antibodies, from one immune egg we can isolate 0.36 mg IgY, this quantity is enough for producing 1800 U activity of Hot start Taq DNA Polymerase.

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