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Tuning Protein Diffusivity with Membrane Tethers

[Image: see text] Diffusion is essential for biochemical processes because it dominates molecular movement on small scales. Enzymatic reactions, for example, require fast exchange of substrate and product molecules in the local environment of the enzyme to ensure efficient turnover. On larger spatia...

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Detalles Bibliográficos
Autores principales: Mörsdorf, David, Müller, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344912/
https://www.ncbi.nlm.nih.gov/pubmed/30562001
http://dx.doi.org/10.1021/acs.biochem.8b01150
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author Mörsdorf, David
Müller, Patrick
author_facet Mörsdorf, David
Müller, Patrick
author_sort Mörsdorf, David
collection PubMed
description [Image: see text] Diffusion is essential for biochemical processes because it dominates molecular movement on small scales. Enzymatic reactions, for example, require fast exchange of substrate and product molecules in the local environment of the enzyme to ensure efficient turnover. On larger spatial scales, diffusion of secreted signaling proteins is thought to limit the spatial extent of tissue differentiation during embryonic development. While it is possible to measure diffusion in vivo, specifically interfering with diffusion processes and testing diffusion models directly remains challenging. The development of genetically encoded nanobodies that bind specific proteins has provided the opportunity to alter protein localization and reduce protein mobility. Here, we extend the nanobody toolbox with a membrane-tethered low-affinity diffusion regulator that can be used to tune the effective diffusivity of extracellular molecules over an order of magnitude in living embryos. This opens new avenues for future applications to functionally interfere with diffusion-dependent processes.
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spelling pubmed-63449122019-01-25 Tuning Protein Diffusivity with Membrane Tethers Mörsdorf, David Müller, Patrick Biochemistry [Image: see text] Diffusion is essential for biochemical processes because it dominates molecular movement on small scales. Enzymatic reactions, for example, require fast exchange of substrate and product molecules in the local environment of the enzyme to ensure efficient turnover. On larger spatial scales, diffusion of secreted signaling proteins is thought to limit the spatial extent of tissue differentiation during embryonic development. While it is possible to measure diffusion in vivo, specifically interfering with diffusion processes and testing diffusion models directly remains challenging. The development of genetically encoded nanobodies that bind specific proteins has provided the opportunity to alter protein localization and reduce protein mobility. Here, we extend the nanobody toolbox with a membrane-tethered low-affinity diffusion regulator that can be used to tune the effective diffusivity of extracellular molecules over an order of magnitude in living embryos. This opens new avenues for future applications to functionally interfere with diffusion-dependent processes. American Chemical Society 2018-12-18 2019-01-22 /pmc/articles/PMC6344912/ /pubmed/30562001 http://dx.doi.org/10.1021/acs.biochem.8b01150 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Mörsdorf, David
Müller, Patrick
Tuning Protein Diffusivity with Membrane Tethers
title Tuning Protein Diffusivity with Membrane Tethers
title_full Tuning Protein Diffusivity with Membrane Tethers
title_fullStr Tuning Protein Diffusivity with Membrane Tethers
title_full_unstemmed Tuning Protein Diffusivity with Membrane Tethers
title_short Tuning Protein Diffusivity with Membrane Tethers
title_sort tuning protein diffusivity with membrane tethers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344912/
https://www.ncbi.nlm.nih.gov/pubmed/30562001
http://dx.doi.org/10.1021/acs.biochem.8b01150
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