Direct Cytosolic Delivery of Proteins Using Lyophilized and Reconstituted Polymer-Protein Assemblies

David C Luther; Harini Nagaraj; Ritabrita Goswami; Yağız Anıl Çiçek; Taewon Jeon; Sanjana Gopalakrishnan; Vincent M Rotello

doi:10.1007/s11095-022-03226-w

Direct Cytosolic Delivery of Proteins Using Lyophilized and Reconstituted Polymer-Protein Assemblies

Pharm Res. 2022 Jun;39(6):1197-1204. doi: 10.1007/s11095-022-03226-w. Epub 2022 Mar 16.

Authors

David C Luther¹, Harini Nagaraj¹, Ritabrita Goswami¹, Yağız Anıl Çiçek¹, Taewon Jeon^{1

2}, Sanjana Gopalakrishnan¹, Vincent M Rotello³

Affiliations

¹ Department of Chemistry, University of Massachusetts, 379A LGRT Tower A, 710 North Pleasant St., Massachusetts, 01003, Amherst, USA.
² Molecular and Cellular Biology Graduate Program, University of Massachusetts, 710 North Pleasant St., Massachusetts, 01003, Amherst, USA.
³ Department of Chemistry, University of Massachusetts, 379A LGRT Tower A, 710 North Pleasant St., Massachusetts, 01003, Amherst, USA. rotello@umass.edu.

Abstract

Purpose: Cytosolic delivery of proteins accesses intracellular targets for chemotherapy and immunomodulation. Current delivery systems utilize inefficient endosomal pathways of uptake and escape that lead to degradation of delivered cargo. Cationic poly(oxanorbornene)imide (PONI) polymers enable highly efficient cytosolic delivery of co-engineered proteins, but aggregation and denaturation in solution limits shelf life. In the present study we evaluate polymer-protein nanocomposite vehicles as candidates for lyophilization and point-of-care resuspension to provide a transferrable technology for cytosolic protein delivery.

Methods: Self-assembled nanocomposites of engineered poly(glutamate)-tagged (E-tagged) proteins and guanidinium-functionalized PONI homopolymers were generated, lyophilized, and stored for 2 weeks. After reconstitution and delivery, cytosolic access of E-tagged GFP cargo (GFP_E15) was assessed through diffuse cytosolic and nuclear fluorescence_, and cell killing with chemotherapeutic enzyme Granzyme A (GrA_E10). Efficiency was quantified between freshly prepared and lyophilized samples.

Results: Reconstituted nanocomposites retained key structural features of freshly prepared assemblies, with minimal loss of material. Cytosolic delivery (> 80% efficiency of freshly prepared nanocomposites) of GFP_E15 was validated in several cell lines, with intracellular access validated and quantified through diffusion into the nucleus. Delivery of GrA_E10 elicited significant tumorigenic cell death. Intracellular access of cytotoxic protein was validated through cell viability.

Conclusion: Reconstituted nanocomposites achieved efficient cytosolic delivery of protein cargo and demonstrated therapeutic applicability with delivery of GrA_E10. Overall, this strategy represents a versatile and highly translatable method for cytosolic delivery of proteins.

Keywords: cytosolic delivery; lyophilization; poly(oxanorbornene)imide; protein delivery; supramolecular.

MeSH terms

Cytosol / metabolism
Endosomes / metabolism
Freeze Drying
Polymers* / chemistry
Proteins* / chemistry

Substances

Polymers
Proteins

Abstract

MeSH terms

Substances

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