Comparison of protein samples
View Patent ↗Methods of qualitatively and/or quantitatively detecting the presence of mutations, modifications or impurities in a protein sample are provided. The methods utilize isotopically labeled variants of amino acids incorporated into proteins prior to protein digest to enable comparisons of two protein samples in bottom-up liquid chromatography.
1. A method of characterizing a protein sample, the method comprising:
(i) providing a sample of a first protein, having a known amino acid sequence, wherein at least one amino acid in the first protein is replaced with an isotopically labeled amino acid comprising at least one heavy isotope;
(ii) providing a sample of a second, unlabeled protein comprising an unlabeled amino acid corresponding to the isotopically labeled variant in the first protein;
(iii) mixing the first sample and the second sample to form a mixture;
(iv) subjecting the mixture to protein digestion to form a first digest, wherein substantially all peptides of the first protein in the digest comprise at least one isotopically labeled amino acid; subjecting the first digest to bottom-up Liquid Chromatography-Mass Spectroscopy to form a first spectra including one or more doublet or singlet peaks, each doublet peak indicating the presence of an isotopically labeled peptide from the first sample and a corresponding unlabeled peptide from the second sample and each singlet peak indicating presence of peptide with a mutation, modification, or impurity, wherein isotopically labeled peptides represented in the first spectra have a combined amino acid sequence that comprises at least 80% of the amino acid sequence of the first protein, wherein unlabeled peptides represented in the first spectra have a combined amino acid sequence that comprises at least 80% of the amino acid sequence of the second protein, and wherein the method is employed to detect a mutation, modification or impurity in the second protein sample, thereby characterizing the second protein sample.
2. The method of claim 1 , further comprising the step of quantifying the amount of the unlabeled chemically distinct peptide based in a relative reduction in peak intensity.
3. The method of claim 1 , wherein substantially all equivalent amino acids in the first protein are isotopically labeled.
4. The method of claim 1 , wherein the protein digestion and the isotopically labeled amino acid are selected from the group consisting of:
(a) trypsin digestion and one or more of heavy arginines, heavy lysines, and combinations thereof;
(b) endoproteinase GluC digestion and heavy glutamic acid;
(c) enterokinase light chain digestion and the isotopically labeled variant is selected from one or more of heavy aspartic acids, heavy lysines, and combinations thereof;
(d) Factor Xa digestion and one or more of heavy isoleucines, heavy glutamic acids, heavy aspartic acids, heavy glycines, heavy arginines, and combinations thereof;
(e) furin digestion and heavy arginine;
(f) genease I digestion and one or more of heavy histidines, heavy tyrosines, and combinations thereof;
(g) chymotrypsin digestion and a heavy aromatic amino acid;
(h) Lys-C or Lys-N digestion and heavy lysine; and
(i) endoproteinase ArgC digestion and heavy arginine.
5. The method of claim 1 , further comprising the step of purifying the labeled protein and the unlabeled protein prior to protein digestion.
6. The method of claim 1 , wherein the labeled and unlabeled proteins are individually selected from the group consisting of a recombinant protein, a biotherapeutic protein, an antibody, a monoclonal antibody, an antibody drug-conjugate, an imaging antibody, a fusion protein, and a pegylated protein.
7. The method of claim 1 , wherein the labeled and unlabeled proteins are antibodies.
8. The method of claim 1 , wherein the digest comprises a population of unlabeled peptides having a combined sequence representing substantially all of the complete amino acid sequence of the unlabeled protein.
9. The method of claim 8 , wherein the combined sequence comprises the complete amino acid sequence of the unlabeled protein.
10. The method of claim 1 , further comprising the steps of:
(i) providing a sample of a third, unlabeled protein comprising an unlabeled amino acid corresponding to the isotopically labeled variant in the first protein;
(ii) mixing the first sample and the third sample to form a second mixture;
(iii) subjecting the second mixture to a second protein digestion to form a second digest; and
(iv) subjecting the second digest to bottom-up Liquid Chromatography-Mass Spectroscopy to form a second spectra including one or more doublet or singlet peaks, each doublet peak indicating the presence of an isotopically labeled peptide from the first sample and a corresponding unlabeled peptide from the third sample and each singlet peak indicating presence of peptide with a mutation, modification, or impurity, thereby characterizing the third protein sample.
11. The method of claim 1 , wherein the first protein sample is an innovator biologic and the second protein sample is a biosimilar of the innovator biologic.
12. The method of claim 1 , wherein the first protein sample is an unconjugated protein and the second protein sample is a conjugated protein.
13. The method of claim 1 , wherein the first and second protein samples are produced in different cell lines, different cell types or different manufacturing processes.
14. The method of claim 1 , wherein the first and second protein samples have been stored under different storage conditions.
15. The method of claim 1 , wherein the mutation, modification or impurity is selected from the group consisting of altered oligosaccharide content, a N-terminal glutamine conversion, C-terminal lysine removal, altered pyroglutamate content, and increased deamidation or oxidation.
16. The method of claim 1 , wherein the first and second samples are substantially homogenous protein preparations.
17. The method of claim 1 , wherein the first and second samples are pharmaceutical compositions.