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Biomolecular condensates with complex architectures via controlled nucleation

Accepted version
Peer-reviewed

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Authors

Verwiel, Madelief AM  ORCID logo  https://orcid.org/0000-0002-4445-937X
Spaepen, Frans A 

Abstract

jats:titleAbstract</jats:title>jats:pThe structure and function of biomolecular condensates are closely related. However, many studies and applications of this relationship are prevented because controlling the mesoscale architecture of condensates can be difficult. Here we introduce a way to create custom multiphase architectures by nucleating new droplets in condensates. This nucleation occurs due to limited diffusion in the dense condensates and a composition change forced upon the system by changing the experimental conditions. The designed architectures are transient states created out of equilibrium. We provide a detailed method for understanding and designing a range of condensate architectures. Access to these long-lived complex architectures will enable researchers to incorporate increasingly sophisticated compartmentalization and functionality in condensates. This general strategy for creating complex structured condensates out of equilibrium may also provide insights into the structure of condensates in cells.</jats:p>

Description

Keywords

40 Engineering, 4016 Materials Engineering, 34 Chemical Sciences

Journal Title

Nature Chemical Engineering

Conference Name

Journal ISSN

2948-1198
2948-1198

Volume Title

Publisher

Springer Science and Business Media LLC
Sponsorship
European Commission Horizon 2020 (H2020) ERC (101001615)
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (101023060)
he research leading to these results has received funding from the Royall Scholarship (N.A.E.), the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant MicroREvolu- tion (agreement no. 101023060; T.S.) the Newman Foundation (T.P.J.K., T.S.), The Dutch Ministry of Education, Culture and Science Gravitation program (024.005.020; J.C.M.H.), the Spinoza premium (J.C.M.H.) and the European Research Council under the European Union’s Horizon 2020 research and innovation program through the ERC grant DiProPhys (agreement ID 101001615;T.P.J.K.).