Cargando…

The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles

BACKGROUND: The high cost of fermentation, purification, cold storage and transportation, short shelf life, and sterile delivery methods of biopharmaceuticals, is a matter for producers and consumers as well. Since the FDA has now approved plant cells for large-scale, cost-effective biopharmaceutica...

Descripción completa

Detalles Bibliográficos
Autores principales: Ehsasatvatan, Maryam, Kohnehrouz, Bahram Baghban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557345/
https://www.ncbi.nlm.nih.gov/pubmed/37798746
http://dx.doi.org/10.1186/s13036-023-00383-3
_version_ 1785117071292497920
author Ehsasatvatan, Maryam
Kohnehrouz, Bahram Baghban
author_facet Ehsasatvatan, Maryam
Kohnehrouz, Bahram Baghban
author_sort Ehsasatvatan, Maryam
collection PubMed
description BACKGROUND: The high cost of fermentation, purification, cold storage and transportation, short shelf life, and sterile delivery methods of biopharmaceuticals, is a matter for producers and consumers as well. Since the FDA has now approved plant cells for large-scale, cost-effective biopharmaceutical production, the isolation and lyophilization of transplastomic chloroplasts can cover concerns about limitations. DARPins are engineered small single-domain proteins that have been selected to bind to HER2 with high affinity and specificity. HER2 is an oncogene involved in abnormal cell growth in some cancers and the target molecule for cancer immunotherapy. RESULTS: In this study, we reported the prolonged stability and functionality of DARPin G3 in lyophilized transplastomic tobacco leaves and chloroplasts. Western blot analysis of lyophilized leaves and chloroplasts stored at room temperature for up to nine months showed that the DARPin G3 protein was stable and preserved proper folding. Lyophilization of leaves and isolated chloroplasts increased DARPin G3 protein concentrations by 16 and 32-fold, respectively. The HER2-binding assay demonstrated that the chloroplast-made DARPin G3 can maintain its stability and binding activity without any affinity drop in lyophilized leaf materials throughout this study for more than nine months at room temperature. CONCLUSION: Lyophilization of chloroplasts expressing DARPin G3 would further reduce costs and simplify downstream processing, purification, and storage. Compressed packages of lyophilized chloroplasts were much more effective than lyophilized transplastomic leaves considering occupied space and downstream extraction and purification of DARPin G3 after nine months. These methods facilitate any relevant formulation practices for these compounds to meet any demand-oriented needs.
format Online
Article
Text
id pubmed-10557345
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-105573452023-10-07 The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles Ehsasatvatan, Maryam Kohnehrouz, Bahram Baghban J Biol Eng Research BACKGROUND: The high cost of fermentation, purification, cold storage and transportation, short shelf life, and sterile delivery methods of biopharmaceuticals, is a matter for producers and consumers as well. Since the FDA has now approved plant cells for large-scale, cost-effective biopharmaceutical production, the isolation and lyophilization of transplastomic chloroplasts can cover concerns about limitations. DARPins are engineered small single-domain proteins that have been selected to bind to HER2 with high affinity and specificity. HER2 is an oncogene involved in abnormal cell growth in some cancers and the target molecule for cancer immunotherapy. RESULTS: In this study, we reported the prolonged stability and functionality of DARPin G3 in lyophilized transplastomic tobacco leaves and chloroplasts. Western blot analysis of lyophilized leaves and chloroplasts stored at room temperature for up to nine months showed that the DARPin G3 protein was stable and preserved proper folding. Lyophilization of leaves and isolated chloroplasts increased DARPin G3 protein concentrations by 16 and 32-fold, respectively. The HER2-binding assay demonstrated that the chloroplast-made DARPin G3 can maintain its stability and binding activity without any affinity drop in lyophilized leaf materials throughout this study for more than nine months at room temperature. CONCLUSION: Lyophilization of chloroplasts expressing DARPin G3 would further reduce costs and simplify downstream processing, purification, and storage. Compressed packages of lyophilized chloroplasts were much more effective than lyophilized transplastomic leaves considering occupied space and downstream extraction and purification of DARPin G3 after nine months. These methods facilitate any relevant formulation practices for these compounds to meet any demand-oriented needs. BioMed Central 2023-10-05 /pmc/articles/PMC10557345/ /pubmed/37798746 http://dx.doi.org/10.1186/s13036-023-00383-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ehsasatvatan, Maryam
Kohnehrouz, Bahram Baghban
The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles
title The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles
title_full The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles
title_fullStr The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles
title_full_unstemmed The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles
title_short The lyophilized chloroplasts store synthetic DARPin G3 as bioactive encapsulated organelles
title_sort lyophilized chloroplasts store synthetic darpin g3 as bioactive encapsulated organelles
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557345/
https://www.ncbi.nlm.nih.gov/pubmed/37798746
http://dx.doi.org/10.1186/s13036-023-00383-3
work_keys_str_mv AT ehsasatvatanmaryam thelyophilizedchloroplastsstoresyntheticdarping3asbioactiveencapsulatedorganelles
AT kohnehrouzbahrambaghban thelyophilizedchloroplastsstoresyntheticdarping3asbioactiveencapsulatedorganelles
AT ehsasatvatanmaryam lyophilizedchloroplastsstoresyntheticdarping3asbioactiveencapsulatedorganelles
AT kohnehrouzbahrambaghban lyophilizedchloroplastsstoresyntheticdarping3asbioactiveencapsulatedorganelles