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Viscosity Regulation of Chemically Simple Condensates.
Le, Nghia T K; Park, Eunbin; Kim, Hyungjun; Park, Jongmin; Kang, Kyungtae.
Affiliation
  • Le NTK; Department of Applied Chemistry, Kyung Hee University, Yongin, Gyeonggi 17104, Republic of Korea.
  • Park E; Department of Chemistry, Kangwon National University, Chuncheon 24341, Republic of Korea.
  • Kim H; Department of Chemistry and Research Institute of Basic Sciences, Incheon National University, Incheon 22012, Republic of Korea.
  • Park J; Department of Chemistry, Kangwon National University, Chuncheon 24341, Republic of Korea.
  • Kang K; Multidimensional Genomics Research Center, Kangwon National University, Chuncheon 24341, Republic of Korea.
Biomacromolecules ; 25(9): 5959-5967, 2024 Sep 09.
Article in En | MEDLINE | ID: mdl-39166772
ABSTRACT
This study investigates the viscosity and liquid-solid transition behavior of biomolecular condensates formed by polyarginine chains (Rx) of varying lengths and citric acid (CA) derivatives. By condensing Rx chains of various lengths with CA derivatives, we showed that the shorter Rx chains attenuate the high aggregation tendency of the longer chains when condensed with CA. A mixture of different Rx lengths exhibited uniform intracondensate distribution, while its mobility largely depended on the ratio of the longer Rx chain. Our findings demonstrate a simple method to modulate condensate properties by adjusting the composition of scaffold molecules, shedding light on the role of molecular composition in controlling condensate viscosity and transition dynamics. This research contributes to a deeper understanding of biomolecular condensation processes and offers insights into potential strategies for manipulating condensate properties for various applications, including in the fields of synthetic biology and disease therapeutics in the future.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptides / Citric Acid Language: En Journal: Biomacromolecules Journal subject: BIOLOGIA MOLECULAR Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptides / Citric Acid Language: En Journal: Biomacromolecules Journal subject: BIOLOGIA MOLECULAR Year: 2024 Document type: Article Country of publication: United States