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Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- ISOLERE BIO INC
- Proposal award date
- 2021-09-15
- Contract end date
- 2022-03-14
- UEI
- U9LXLSXNME74
- Solicitation number
- PA20-260
- Topic code
- 400
Research abstract
Project Summary
The goal of this Phase I SBIR project is to develop a novel purification method that is compatible with in vitro
transcription (IVT)-based manufacturing of RNA for use as a therapeutic or vaccine. As RNA becomes more
commonly used for pharmaceutical products, manufacturing methods must improve their scalability, speed, and
cost-effectiveness. There are several pain points in RNA manufacturing. First, current affinity resins have very
low capacity —only ~2mg RNA per mL— necessitating large volumes of resin at commercial scale. These resins
are priced at over $25,000 per liter, rendering commercial scale production extremely costly. Second, 5’ capping
of RNA – essential for in vivo function – and the subsequent removal of any residual uncapped RNA is a major
bottleneck for RNA production. Isolere Bio, Inc. specializes in designing innovative purification solutions that
combine a protein affinity tag that is genetically fused to an elastin-like polypeptide (ELP). This reagent is capable
of temperature or salt-controlled phase separation that enables capture of a specific target regardless of its
complexity or the presence of other impurities. We will develop a novel combination of biopolymers, referred to
here as IVTag™, that enables simultaneous RNA sequestration into concentrated, pure liquid droplets and
methylation of transcripts. Two ELP fusion proteins will be developed: one will contain an RNA-binding motif and
the second an O’-methyltransferase (O’-MTase) enzyme, responsible for 5’-capping of RNA. We will then
develop platform methods for simultaneous purification of RNA into droplets and high efficiency capping of the
sequestered RNA. This Phase I program is designed to demonstrate compatibility of this essential IVT enzyme
and complexing it with Isolere’s non-chromatographic purification methods. Key activities of the proposal include
synthesizing, purifying, and testing each biopolymer fusions’ functionality and then evaluating their efficacy when
applied in tandem and comparing process efficiency to the industry standard method. If successful, additional
functionality of the RNA micro-crucible will be developed in Phase II in the form of a T7 polymerase-ELP fusion
(for initial transcription of a DNA template) and a Poly-A polymerase-ELP fusion (for adding a 3’ poly-A tail to
transcripts). Our vision is to ultimately create a fully continuous RNA manufacturing process in smart droplets.
These smart droplets are expected to support a straightforward, scalable, and cost-effective manufacturing
workflow with micro-crucibles capable of carrying out a complex series of processing steps. Because the micro-
crucible is volume independent, the scale-up difficulties associated with affinity resins are eliminated. In addition,
with other applications of Isolere’s technology, including to antibodies and viral vectors, the ELP fusion reagents
have proven to be easily manufacturable and re-usable for multiple purification cycles, reducing costs of goods
significantly compared to affinity resins. The scalability, robust performance, and cost-effectiveness of the
proposed product is an excellent fit for accelerating the development of therapeutic RNA candidates from bench
scale discovery through large-scale manufacturing of commercial products.Project Narrative
As RNA becomes a mainstream therapeutic, manufacturing methods must become cost-effective and scalable
to keep pace with an increasing number of patients, up to and including vaccination of the global population.
Isolere Bio, Inc. has developed several purification solutions that feature an affinity tag fused to a smart
biopolymer; this reagent specifically endows any target biologic with reversible soluble to insoluble behavior that
enables affinity capture, concentration, and contaminant removal to occur in micro-crucible droplets. This Phase
I research program will establish proof-of-concept of Isolere’s scalable and efficient approach to manufacturing
RNA drugs and vaccines.
Technology keywords
Not reported
Other awards by this recipient
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Research funding history
8 SBIR/STTR records share this UEI (2018–2022). Reported award amounts total $4,323,256. Reported amounts are not federal obligations.
Phases: Phase I, Phase II
Agencies: Department of Health and Human Services, National Science Foundation
Agency intelligence
Department of Health and Human Services
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