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An improved 96-well turbidity assay for T4 lysozyme activity

T4 lysozyme (T4L) is an important model system for investigating the relationship between protein structure and function. Despite being extensively studied, a reliable, quantitative activity assay for T4L has not been developed. Here, we present an improved T4L turbidity assay as well as an affinity...

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Detalles Bibliográficos
Autores principales: Toro, Tasha B., Nguyen, Thao P., Watt, Terry J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487725/
https://www.ncbi.nlm.nih.gov/pubmed/26150996
http://dx.doi.org/10.1016/j.mex.2015.05.004
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author Toro, Tasha B.
Nguyen, Thao P.
Watt, Terry J.
author_facet Toro, Tasha B.
Nguyen, Thao P.
Watt, Terry J.
author_sort Toro, Tasha B.
collection PubMed
description T4 lysozyme (T4L) is an important model system for investigating the relationship between protein structure and function. Despite being extensively studied, a reliable, quantitative activity assay for T4L has not been developed. Here, we present an improved T4L turbidity assay as well as an affinity-based T4L expression and purification protocol. This assay is designed for 96-well format and utilizes conditions amenable for both T4L and other lysozymes. This protocol enables easy, efficient, and quantitative characterization of T4L variants and allows comparison between different lysozymes. Our method: • Is applicable for all lysozymes, with enhanced sensitivity for T4 lysozyme compared to other 96-well plate turbidity assays; • Utilizes standardized conditions for comparing T4 lysozyme variants and other lysozymes; and • Incorporates a simplified expression and purification protocol for T4 lysozyme.
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spelling pubmed-44877252015-07-06 An improved 96-well turbidity assay for T4 lysozyme activity Toro, Tasha B. Nguyen, Thao P. Watt, Terry J. MethodsX Biochemistry, Genetics and Molecular Biology T4 lysozyme (T4L) is an important model system for investigating the relationship between protein structure and function. Despite being extensively studied, a reliable, quantitative activity assay for T4L has not been developed. Here, we present an improved T4L turbidity assay as well as an affinity-based T4L expression and purification protocol. This assay is designed for 96-well format and utilizes conditions amenable for both T4L and other lysozymes. This protocol enables easy, efficient, and quantitative characterization of T4L variants and allows comparison between different lysozymes. Our method: • Is applicable for all lysozymes, with enhanced sensitivity for T4 lysozyme compared to other 96-well plate turbidity assays; • Utilizes standardized conditions for comparing T4 lysozyme variants and other lysozymes; and • Incorporates a simplified expression and purification protocol for T4 lysozyme. Elsevier 2015-05-18 /pmc/articles/PMC4487725/ /pubmed/26150996 http://dx.doi.org/10.1016/j.mex.2015.05.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Toro, Tasha B.
Nguyen, Thao P.
Watt, Terry J.
An improved 96-well turbidity assay for T4 lysozyme activity
title An improved 96-well turbidity assay for T4 lysozyme activity
title_full An improved 96-well turbidity assay for T4 lysozyme activity
title_fullStr An improved 96-well turbidity assay for T4 lysozyme activity
title_full_unstemmed An improved 96-well turbidity assay for T4 lysozyme activity
title_short An improved 96-well turbidity assay for T4 lysozyme activity
title_sort improved 96-well turbidity assay for t4 lysozyme activity
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487725/
https://www.ncbi.nlm.nih.gov/pubmed/26150996
http://dx.doi.org/10.1016/j.mex.2015.05.004
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