Comb-like Pseudopeptides Enable Very Rapid and Efficient Intracellular Trehalose Delivery for Enhanced Cryopreservation of Erythrocytes.


Journal

ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991

Informations de publication

Date de publication:
01 Jul 2020
Historique:
pubmed: 5 6 2020
medline: 2 3 2021
entrez: 5 6 2020
Statut: ppublish

Résumé

Cell cryopreservation plays a key role in the development of reproducible and cost-effective cell-based therapies. Trehalose accumulated in freezing- and desiccation-tolerant organisms in nature has been sought as an attractive nontoxic cryoprotectant. Herein, we report a coincubation method for very rapid and efficient delivery of membrane-impermeable trehalose into ovine erythrocytes through reversible membrane permeabilization using pH-responsive, comb-like pseudopeptides. The pseudopeptidic polymers containing relatively long alkyl side chains were synthesized to mimic membrane-anchoring fusogenic proteins. The intracellular trehalose delivery efficiency was optimized by manipulating the side chain length, degree of substitution, and concentration of the pseudopeptides with different hydrophobic alkyl side chains, the pH, temperature, and time of incubation, as well as the polymer-to-cell ratio and the concentration of extracellular trehalose. Treatment of erythrocytes with the comb-like pseudopeptides for only 15 min yielded an intracellular trehalose concentration of 177.9 ± 8.6 mM, which resulted in 90.3 ± 0.7% survival after freeze-thaw. The very rapid and efficient delivery was found to be attributed to the reversible, pronounced membrane curvature change as a result of strong membrane insertion of the comb-like pseudopeptides. The pseudopeptides can enable efficient intracellular delivery of not only trehalose for improved cell cryopreservation but also other membrane-impermeable cargos.

Identifiants

pubmed: 32496048
doi: 10.1021/acsami.0c03260
doi:

Substances chimiques

Cryoprotective Agents 0
Polymers 0
Trehalose B8WCK70T7I

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

28941-28951

Auteurs

Siyuan Chen (S)

Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

Liwei Wu (L)

Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

Jie Ren (J)

Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

Victoria Bemmer (V)

Department of Materials, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

Richard Zajicek (R)

Cell & Gene Therapy Platform CMC, Platform Technology & Sciences, GlaxoSmithKline plc R&D, Gunnels Wood, Stevenage, Hertfordshire SG1 2NY, U.K.

Rongjun Chen (R)

Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

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Classifications MeSH