Cargando…

Speeding up biomolecular interactions by molecular sledding

Numerous biological processes involve association of a protein with its binding partner, an event that is preceded by a diffusion-mediated search bringing the two partners together. Often hindered by crowding in biologically relevant environments, three-dimensional diffusion can be slow and result i...

Descripción completa

Detalles Bibliográficos
Autores principales: Turkin, Alexander, Zhang, Lei, Marcozzi, Alessio, Mangel, Walter F., Herrmann, Andreas, van Oijen, Antoine M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762599/
https://www.ncbi.nlm.nih.gov/pubmed/26913169
http://dx.doi.org/10.1039/c5sc03063c
_version_ 1782417134311178240
author Turkin, Alexander
Zhang, Lei
Marcozzi, Alessio
Mangel, Walter F.
Herrmann, Andreas
van Oijen, Antoine M.
author_facet Turkin, Alexander
Zhang, Lei
Marcozzi, Alessio
Mangel, Walter F.
Herrmann, Andreas
van Oijen, Antoine M.
author_sort Turkin, Alexander
collection PubMed
description Numerous biological processes involve association of a protein with its binding partner, an event that is preceded by a diffusion-mediated search bringing the two partners together. Often hindered by crowding in biologically relevant environments, three-dimensional diffusion can be slow and result in long bimolecular association times. Similarly, the initial association step between two binding partners often represents a rate-limiting step in biotechnologically relevant reactions. We demonstrate the practical use of an 11-a.a. DNA-interacting peptide derived from adenovirus to reduce the dimensionality of diffusional search processes and speed up associations between biological macromolecules. We functionalize binding partners with the peptide and demonstrate that the ability of the peptide to one-dimensionally diffuse along DNA results in a 20-fold reduction in reaction time. We also show that modifying PCR primers with the peptide sled enables significant acceleration of standard PCR reactions.
format Online
Article
Text
id pubmed-4762599
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-47625992016-02-22 Speeding up biomolecular interactions by molecular sledding Turkin, Alexander Zhang, Lei Marcozzi, Alessio Mangel, Walter F. Herrmann, Andreas van Oijen, Antoine M. Chem Sci Chemistry Numerous biological processes involve association of a protein with its binding partner, an event that is preceded by a diffusion-mediated search bringing the two partners together. Often hindered by crowding in biologically relevant environments, three-dimensional diffusion can be slow and result in long bimolecular association times. Similarly, the initial association step between two binding partners often represents a rate-limiting step in biotechnologically relevant reactions. We demonstrate the practical use of an 11-a.a. DNA-interacting peptide derived from adenovirus to reduce the dimensionality of diffusional search processes and speed up associations between biological macromolecules. We functionalize binding partners with the peptide and demonstrate that the ability of the peptide to one-dimensionally diffuse along DNA results in a 20-fold reduction in reaction time. We also show that modifying PCR primers with the peptide sled enables significant acceleration of standard PCR reactions. Royal Society of Chemistry 2016-02-01 2015-10-07 /pmc/articles/PMC4762599/ /pubmed/26913169 http://dx.doi.org/10.1039/c5sc03063c Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Turkin, Alexander
Zhang, Lei
Marcozzi, Alessio
Mangel, Walter F.
Herrmann, Andreas
van Oijen, Antoine M.
Speeding up biomolecular interactions by molecular sledding
title Speeding up biomolecular interactions by molecular sledding
title_full Speeding up biomolecular interactions by molecular sledding
title_fullStr Speeding up biomolecular interactions by molecular sledding
title_full_unstemmed Speeding up biomolecular interactions by molecular sledding
title_short Speeding up biomolecular interactions by molecular sledding
title_sort speeding up biomolecular interactions by molecular sledding
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762599/
https://www.ncbi.nlm.nih.gov/pubmed/26913169
http://dx.doi.org/10.1039/c5sc03063c
work_keys_str_mv AT turkinalexander speedingupbiomolecularinteractionsbymolecularsledding
AT zhanglei speedingupbiomolecularinteractionsbymolecularsledding
AT marcozzialessio speedingupbiomolecularinteractionsbymolecularsledding
AT mangelwalterf speedingupbiomolecularinteractionsbymolecularsledding
AT herrmannandreas speedingupbiomolecularinteractionsbymolecularsledding
AT vanoijenantoinem speedingupbiomolecularinteractionsbymolecularsledding