Protocol for screening and validating antibodies specific to protein phosphorylation sites using a set of yeast biopanning approaches
Developing antibodies with high specificity against post-translationally modified epitopes remains a challenge. Yeast biopanning is well suited in screening for high-specificity binders. Here, we present a protocol for screening and validating antibodies specific to protein phosphorylation sites usi...
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Veröffentlicht in: | STAR protocols 2024-09, Vol.5 (3), p.103241, Article 103241 |
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Sprache: | eng |
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Zusammenfassung: | Developing antibodies with high specificity against post-translationally modified epitopes remains a challenge. Yeast biopanning is well suited in screening for high-specificity binders. Here, we present a protocol for screening and validating antibodies specific to protein phosphorylation sites using a set of yeast biopanning approaches. We describe steps for screening a yeast surface display library for antibodies and other binders. We then detail procedures for validating the antibodies found by analyzing their specificity through whole-well image analysis in 96-well plates.
For complete details on the use and execution of this protocol, please refer to Arbaciauskaite et al.1
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•A yeast biopanning approach for screening post-translational modification-specific binders•Rigorous quantitative validation of post-translational modification-specific binders•A whole-well image analysis pipeline for yeast biopanning
Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
Developing antibodies with high specificity against post-translationally modified epitopes remains a challenge. Yeast biopanning is well suited in screening for high-specificity binders. Here, we present a protocol for screening and validating antibodies specific to protein phosphorylation sites using a set of yeast biopanning approaches. We describe steps for screening a yeast surface display library for antibodies and other binders. We then detail procedures for validating the antibodies found by analyzing their specificity through whole-well image analysis in 96-well plates. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2024.103241 |