Site-specific chemical and topological modifications to augment mRNA therapeutic potential

Synthetic mRNA has emerged as a promising therapeutic platform for the treatment of a wide variety of diseases. Despite clinical demonstrations of mRNA for SARS-CoV-2 vaccines, mRNAs remain limited in application by their susceptibility to nucleases and overall short expression lifetime in vivo. We investigated the site-specific installation of chemical and topological modifications into therapeutic mRNA to augment their expression in cell cultures and mouse models. We began by developing messenger oligonucleotide-conjugated RNAs (mocRNAs), which are mRNAs ligated to modified oligonucleotides that contain 3’ nuclease-resistant modifications. We show that mocRNAs are subject to slower deadenylation and enhance therapeutic protein expression in cell lines and primary cell cultures. We expanded on this technology by creating mRNAs with chemically branched poly(A) tails, or multitail mRNAs, which increase the density of modifications at the 3’ end of mocRNA and further stabilize mRNA against deadenylation. In conjunction with increased nuclease resistance at the 3’ terminus, we developed a strategy to enhance translation initiation on circular mRNAs (circRNAs). We developed QRNAs, which are circRNAs that possess an unnaturally-linked inverted 7-methylguanosine (m7G) cap. QRNAs substantially outperform conventional circRNAs, given the low translation initiation efficiency of IRES compared to cap-dependent initiation. Ultimately, our studies exploring the chemical and topological space of mRNA demonstrates the value of site-specific chemical and topological modifications for designing future generations of designer mRNA-based therapeutics.

Name thesis:degree_name

Doctoral

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Biological Engineering

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2024

Author dc:creator

• Aditham, Abhishek J.

Advisors dc:contributor.advisor

• Wang, Xiao
• Zhang, Feng

Statement dc:rights

• In Copyright - Educational Use Permitted
• Copyright retained by author(s)

Licence dc:rights.uri

• https://rightsstatements.org/page/InC-EDU/1.0/

Handle dc:identifier.uri

https://hdl.handle.net/1721.1/157875

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/157875