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1.
Protein Sci ; 33(9): e5148, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-39180484

RESUMEN

In protein design, the ultimate test of success is that the designs function as desired. Here, we discuss the utility of cell free protein synthesis (CFPS) as a rapid, convenient and versatile method to screen for activity. We champion the use of CFPS in screening potential designs. Compared to in vivo protein screening, a wider range of different activities can be evaluated using CFPS, and the scale on which it can easily be used-screening tens to hundreds of designed proteins-is ideally suited to current needs. Protein design using physics-based strategies tended to have a relatively low success rate, compared with current machine-learning based methods. Screening steps (such as yeast display) were often used to identify proteins that displayed the desired activity from many designs that were highly ranked computationally. We also describe how CFPS is well-suited to identify the reasons designs fail, which may include problems with transcription, translation, and solubility, in addition to not achieving the desired structure and function.


Asunto(s)
Sistema Libre de Células , Biosíntesis de Proteínas , Proteínas , Proteínas/química , Proteínas/metabolismo , Sistema Libre de Células/metabolismo , Ingeniería de Proteínas/métodos
2.
Front Bioeng Biotechnol ; 10: 915035, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35875503

RESUMEN

We present a new method for the surface capture of proteins in cell-free protein synthesis (CFPS). We demonstrate the spontaneous self-assembly of the protein BslA into functionalizable surfaces on the surface of a CFPS reaction chamber. We show that proteins can be covalently captured by such surfaces, using "Catcher/Tag" technology. Importantly, proteins of interest can be captured either when synthesised in situ by CFPS above the BslA surfaces, or when added as pure protein. The simplicity and cost efficiency of this method suggest that it will find many applications in cell-free-based methods.

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