In this case, the technology was improved based upon the surprising discovery that the TAPBPR chaperone acts catalytically on MHC-I-placeholder peptide complexes to create peptide receptive MHC-I species.
Technology is identical to that described in 2018-408-0, except that the ratio of TAPBPR to MHC-I-placeholder peptide complex is less than 1:1. As low as a 1:10,000 ratio of TAPBPR to MHC-I placeholder peptide can be used without an effect on the overall reaction time.
Peptide receptive MHC-I multimer reagents
MHC-I reagents
Identifying antigenic peptides
Identifying and purifying T cell populations
Improved cost effectiveness of making MHC Class I reagents because less of the TAPBPR component needs to be made.
Additional patent claims close off potential loophole in coverage
Country | Type | Number | Dated | Case |
United States Of America | Published Application | 20230059548 | 02/23/2023 | 2019-975 |
European Patent Office | Published Application | EP 4 136 098 | 02/22/2023 | 2020-284 |
European Patent Office | Published Application | 4085069 | 11/09/2022 | 2019-975 |
European Patent Office | Published Application | 4085068 | 11/09/2022 | 2020-297 |
European Patent Office | Published Application | 402841.2 | 07/20/2022 | 2020-251 |
United States Of America | Published Application | 20210371499 | 12/20/2021 | 2020-284 |
United States Of America | Published Application | 20210155670 | 05/27/2021 | 2020-251 |
Additional Patents Pending
MHC-I, Class I MHC, Antigenic Peptide, Peptide Receptive MHC, MHC multimers, MHC tetramers, MHC reagents, Major Histocompatability Complex, Class I, Chaperone, TAPBPR, Catalytic TAPBPR