R41GM142336
Project Grant
Overview
Grant Description
Universal Affinity Membrane Chromatography for Rapid, One-Step Purification of Proteins - Project Summary
The goal of this STTR Phase I project is to demonstrate the feasibility of developing the first universal affinity membrane for the rapid, selective, one-step purification of difficult-to-purify proteins. Despite the urgency for expanding the application of gene editing systems and accelerating vaccine and antibody test development, the rapid purification of critical proteins such as CRISPR-Cas9 and the SARS-CoV2 spike protein with high yield, high purity, and high activity remains a difficult challenge.
The proposed innovation will benefit public health and have a significant impact on the biopharmaceutical industry by addressing this challenge. The products of this innovation will be first-in-market universal affinity membrane chromatography columns based on Trialtus' ultrahigh affinity CL7/IM7 purification system. Research will be done in partnership with Clemson University and the University of Alabama at Birmingham.
Purification of CRISPR-Cas9 protein from E. coli lysate will be used as a demonstration case for evaluating the performance of the affinity membrane innovation. The specific aims of this Phase I study are to (1) synthesize and characterize IM7-activated affinity membranes and (2) test prototype affinity membrane columns for capture purification of CRISPR-Cas9.
In Specific Aim 1, we will establish the feasibility of synthesizing the affinity membranes by immobilizing four IM7 ligand variants at high density on polymer-grafted macroporous membranes. We will measure protein binding capacity, recovery, and column reusability in screening experiments using purified, CL7-tagged CRISPR-Cas9.
In Specific Aim 2, we will quantify and benchmark performance for capture step purification of CRISPR-Cas9 from E. coli lysate. We will measure Cas9 binding capacity, recovery, purity, and activity.
In Phase II, the team plans to comprehensively evaluate the roles that synthesis conditions and membrane support structure play on binding capacity; delineate operating ranges that maximize productivity, recovery, purity, and activity; collaborate with a membrane technology company on research to establish a scalable process to produce membrane columns for external validation; and conduct field research with external partners and prospective customers.
Commercialization will bring the first universal affinity membrane chromatography column to the market. Market entry for the new column products will be to research and development scientists. The columns will provide a universal platform for the rapid, cost-effective purification of tag-free proteins with high yield, purity, and activity. By simplifying purification protocols and reducing purification times, products derived from this membrane innovation will have a major impact in the race to develop new protein drugs, gene therapies, vaccines, and antibody test kits.
The goal of this STTR Phase I project is to demonstrate the feasibility of developing the first universal affinity membrane for the rapid, selective, one-step purification of difficult-to-purify proteins. Despite the urgency for expanding the application of gene editing systems and accelerating vaccine and antibody test development, the rapid purification of critical proteins such as CRISPR-Cas9 and the SARS-CoV2 spike protein with high yield, high purity, and high activity remains a difficult challenge.
The proposed innovation will benefit public health and have a significant impact on the biopharmaceutical industry by addressing this challenge. The products of this innovation will be first-in-market universal affinity membrane chromatography columns based on Trialtus' ultrahigh affinity CL7/IM7 purification system. Research will be done in partnership with Clemson University and the University of Alabama at Birmingham.
Purification of CRISPR-Cas9 protein from E. coli lysate will be used as a demonstration case for evaluating the performance of the affinity membrane innovation. The specific aims of this Phase I study are to (1) synthesize and characterize IM7-activated affinity membranes and (2) test prototype affinity membrane columns for capture purification of CRISPR-Cas9.
In Specific Aim 1, we will establish the feasibility of synthesizing the affinity membranes by immobilizing four IM7 ligand variants at high density on polymer-grafted macroporous membranes. We will measure protein binding capacity, recovery, and column reusability in screening experiments using purified, CL7-tagged CRISPR-Cas9.
In Specific Aim 2, we will quantify and benchmark performance for capture step purification of CRISPR-Cas9 from E. coli lysate. We will measure Cas9 binding capacity, recovery, purity, and activity.
In Phase II, the team plans to comprehensively evaluate the roles that synthesis conditions and membrane support structure play on binding capacity; delineate operating ranges that maximize productivity, recovery, purity, and activity; collaborate with a membrane technology company on research to establish a scalable process to produce membrane columns for external validation; and conduct field research with external partners and prospective customers.
Commercialization will bring the first universal affinity membrane chromatography column to the market. Market entry for the new column products will be to research and development scientists. The columns will provide a universal platform for the rapid, cost-effective purification of tag-free proteins with high yield, purity, and activity. By simplifying purification protocols and reducing purification times, products derived from this membrane innovation will have a major impact in the race to develop new protein drugs, gene therapies, vaccines, and antibody test kits.
Awardee
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Alabama
United States
Geographic Scope
State-Wide
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 05/14/22 to 05/14/23 and the total obligations have decreased from $256,576 to $256,571.
Trialtus Bioscience was awarded
Project Grant R41GM142336
worth $256,571
from the National Institute of General Medical Sciences in September 2021 with work to be completed primarily in Alabama United States.
The grant
has a duration of 1 year 8 months and
was awarded through assistance program 93.859 Biomedical Research and Research Training.
The Project Grant was awarded through grant opportunity PHS 2020-2 Omnibus Solicitation of the NIH for Small Business Technology Transfer Grant Applications (Parent STTR [R41/R42] Clinical Trial Not Allowed).
SBIR Details
Research Type
STTR Phase I
Title
Universal affinity membrane chromatography for rapid, one-step purification of proteins
Abstract
Project Summary The goal of this STTR Phase I project is to demonstrate the feasibility of developing the first universal affinity membrane for the rapid, selective, one-step purification of difficult-to-purify proteins. Despite the urgency for expanding the application of gene editing systems and accelerating vaccine and antibody test development, the rapid purification of critical proteins such as CRISPR-Cas9 and the SARS-COV2 spike protein with high yield, high purity, and high activity remains a difficult challenge. The proposed innovation will benefit public health and have a significant impact on the biopharmaceutical industry by addressing this challenge. The products of this innovation will be first-in-market universal affinity membrane chromatography columns based on TriAltus’ ultrahigh affinity CL7/Im7 purification system. Research will be done in partnership with Clemson University and the University of Alabama at Birmingham. Purification of CRISPR-Cas9 protein from E. coli lysate will be used as a demonstration case for evaluating the performance of the affinity membrane innovation. The Specific Aims of this Phase I study are to (1) Synthesize and characterize Im7-activated affinity membranes and (2) Test prototype affinity membrane columns for capture purification of CRISPR-Cas9. In Specific Aim 1, we will establish the feasibility of synthesizing the affinity membranes by immobilizing four Im7 ligand variants at high density on polymer-grafted macroporous membranes. We will measure protein binding capacity, recovery, and column reusability in screening experiments using purified, CL7-tagged CRISPR-Cas9. In Specific Aim 2, we will quantify and benchmark performance for capture step purification of CRISPR-Cas9 from E. Coli lysate. We will measure Cas9 binding capacity, recovery, purity, and activity. In Phase II, the team plans to comprehensively evaluate the roles that synthesis conditions and membrane support structure play on binding capacity; delineate operating ranges that maximize productivity, recovery, purity, and activity; collaborate with a membrane technology company on research to establish a scalable process to produce membrane columns for external validation; and conduct field research with external partners and prospective customers. Commercialization will bring the first universal affinity membrane chromatography column to the market. Market entry for the new column products will be to research and development scientists. The columns will provide a universal platform for the rapid, cost-effective purification of tag-free proteins with high yield, purity, and activity. By simplifying purification protocols and reducing purification times, products derived from this membrane innovation will have a major impact in the race to develop new protein drugs, gene therapies, vaccines, and antibody test kits.Public Health Relevance Statement The goal of this STTR Phase I project is to develop a universal affinity membrane purification technology based on TriAltus’ ultra-high-affinity CL7/Im7 system. The proposed technology will benefit public health and have a significant impact on the biopharmaceutical industry as a universal platform for the rapid, one step purification of difficult-to-isolate proteins such as CRISPR-Cas9 enzyme and the spike protein from SARS- COV2, which is critically important for expanding the application of gene editing systems and accelerating vaccine and antibody test development.
Topic Code
400
Solicitation Number
PA20-265
Status
(Complete)
Last Modified 10/5/23
Period of Performance
9/15/21
Start Date
5/14/23
End Date
Funding Split
$256.6K
Federal Obligation
$0.0
Non-Federal Obligation
$256.6K
Total Obligated
Activity Timeline
Transaction History
Modifications to R41GM142336
Additional Detail
Award ID FAIN
R41GM142336
SAI Number
R41GM142336-844463591
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75NS00 NIH NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
Funding Office
75NS00 NIH NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
Awardee UEI
LRBNAQ9B51J7
Awardee CAGE
81TX1
Performance District
AL-07
Senators
Tommy Tuberville
Katie Britt
Katie Britt
Modified: 10/5/23