Thermo-sensitive polycaprolactone coacervates for preventing protein aggregation under thermal stress

Inspired from heat shock proteins (HSPs), a thermo-sensitive coacervate-forming polycaprolactone (CPCL) was designed as a natural chaperone mimic to protect proteins from thermal stress. Unlike the coil-globule polymers of poly(<i>N</i>-isopropyl acrylamide) (PNIPAM), the as-designed CPCL underwent a partial dehydration during heating, characterizing it as a coacervate-forming polymer. With its ability to transform between the coil and coacervate states in response to temperature, theCPCL spontaneously captured and released targeted proteins, thereby behaving like a natural chaperone of HSPs. Remarkably, compared with the PNIPAM homopolymer, the CPCL provided more efficient protection for proteins by inhibiting heat-induced aggregation above the melting temperature (<i>T</i><sub>m</sub>). Taken together, we envision that the CPCL with excellent biodegradability and biocompatibility could be a safe excipient for protein protection against thermal damage without separation.

Authors

Institutions

Publication Details

Journal
Journal of Materials Chemistry B
Published
2025-01-01
DOI
https://doi.org/10.1039/d4tb02450h
Primary Topic
Protein purification and stability
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Thermo-sensitive polycaprolactone coacervates for preventing protein aggregation under thermal stress

Meidong Lang, Lianlei Wen, Xinyue Zheng, Yan Xiao
Journal of Materials Chemistry B
Protein purification and stability
article

Thermo-sensitive polycaprolactone coacervates for preventing protein aggregation under thermal stress

Meidong Lang, Lianlei Wen, Xinyue Zheng, Yan Xiao
article en

Abstract

Inspired from heat shock proteins (HSPs), a thermo-sensitive coacervate-forming polycaprolactone (CPCL) was designed as a natural chaperone mimic to protect proteins from thermal stress. Unlike the coil-globule polymers of poly(<i>N</i>-isopropyl acrylamide) (PNIPAM), the as-designed CPCL underwent a partial dehydration during heating, characterizing it as a coacervate-forming polymer. With its ability to transform between the coil and coacervate states in response to temperature, theCPCL spontaneously captured and released targeted proteins, thereby behaving like a natural chaperone of HSPs. Remarkably, compared with the PNIPAM homopolymer, the CPCL provided more efficient protection for proteins by inhibiting heat-induced aggregation above the melting temperature (<i>T</i><sub>m</sub>). Taken together, we envision that the CPCL with excellent biodegradability and biocompatibility could be a safe excipient for protein protection against thermal damage without separation.

Journal of Materials Chemistry BVol. 13(7)
East China University of Science and Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Clean water and sanitation
Openalex Percentile: Top 100%
Protein purification and stability
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Thermo-sensitive polycaprolactone coacervates for preventing protein aggregation under thermal stress — Meidong Lang, Lianlei Wen, et al. · Journal of Materials Chemistry B (2025) | TGRS Research Map | TGRS