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to express simultaneously a variant of the oxygen-evolving enzyme Photosystem II (PSII) and proteins involved in the sulfur metabolism. Among these proteins, we have identified the flavoprotein sulfide-quinone
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determinants underlying natural catalytic strategies of drug-target heme enzymes and their bioresistance. Our approach of engineering redox-active Trp(s) resulting in controlled Trp radical(s) as substrate
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projects aimed at characterizing new microtubule-modifying enzymes. Biochemistry (western blots, protein purification, enzyme assays, etc.) Molecular biology (qPCR, cloning, mutagenesis, etc.) Cell culture
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reactor. The project focuses on the development of multi-catalytic hybrid materials (MCHMs), in which photocatalysts and enzymes will be co-immobilized on a common support. The Laboratoire Lorrain de Chimie
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. The researcher will be supervised by Dr. Robert Wojcieszak and Dr. Nadia Canilho (L2CM). Most of the equipment needed for the project is available on site. Where to apply Website https://emploi.cnrs.fr/Offres/CDD
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The postdoc will realize an EPR analysis on DNA-based enzymes, using 1D and 2D techniques. Two main systems will be investigated, having Copper(II) and Manganese(II) as metal co-factor. Structural and
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substrates using DNA PAINT experiments to analyze the distances between these proteins on a nanometer scale in intact cells. This should reflect the probability of the enzyme to cleave a given protein in the