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Temperature-jump microscopy and interaction of Hsp70 heat shock protein with a client protein in vivo. | LitMetric

Temperature-jump microscopy and interaction of Hsp70 heat shock protein with a client protein in vivo.

Methods

Center for Biophysics and Quantitative Biology, University of Illinois Urbana Champaign, Urbana 61801, USA; Department of Physics, University of Illinois Urbana Champaign, Urbana 61801, USA; Department of Chemistry and Carle-Illinois College of Medicine, University of Illinois Urbana Champaign, Urbana 61801, USA. Electronic address:

Published: November 2024

Biomolecular processes such as protein-protein interactions can depend strongly on cell type and even vary within a single cell type. Here we develop a microscope with a Peltier-controlled temperature stage, a laser temperature jump to induce heat stress, and an autofocusing feature to mitigate temperature drift during experiments, to study a protein-protein interaction in a selected cell type within a live organism, the zebrafish larva. As an application of the instrument, we show that there is considerable cell-to-cell variation of the heat shock protein Hsp70 binding to one of its clients, phosphoglycerate kinase in vivo. We adapt a key feature from our previous folding study, rare transformation of cells within the larva, so that individual cells can be imaged and differentiated for cell-to-cell response. Our approach can be extended to other organisms and cell types than the ones demonstrated in this work.

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Source
http://dx.doi.org/10.1016/j.ymeth.2024.09.019DOI Listing

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