Mass spectrometry analysis of mutant polypeptides in biological samples

Patent metadata

Field	Value
Publication number	US-10670606-B2
Application number	US-201816034610-A
Country	US
Kind code	B2
Filing date	Jul 13, 2018
Priority date	Feb 1, 2010
Publication date	Jun 2, 2020
Grant date	Jun 2, 2020

Abstract

The invention relates to a method for determining the presence of at least one distinct polypeptide in a biological sample comprising contacting the biological sample with a hydrolyzing agent, wherein the hydrolyzing agent is capable of hydrolyzing the distinct polypeptide in a sequence-specific manner such that at least one distinct peptide having a predetermined peptide measured accurate mass would result if the at least one distinct polypeptide were present in the biological sample, to obtain a hydrolyzed sample; bringing the hydrolyzed sample in contact with a substrate comprising at least one immobilized binding partner, wherein the at least one immobilized binding partner is capable of specifically binding the distinct peptide; removing the hydrolyzed sample from the substrate in a manner such that the distinct peptide would remain bound to the immobilized binding partner; contacting the substrate with an elution solution, wherein the distinct peptide would dissociate from the immobilized binding partner into the elution solution; subjecting a portion of the elution solution to liquid chromatography to segregate a plurality of molecules in the portion of the elution solution to obtain sorted molecules; determining the measured accurate mass of at least one sorted molecule present in the elution solution; and determining the presence of the at least one distinct polypeptide in the biological sample when a measured accurate mass of at least one molecule is substantially equal to the predetermined peptide measured accurate mass.

First claim

What is claimed is:

1. A method for determining the presence of at least one distinct polypeptide in a biological sample, wherein the at least one distinct polypeptide contains a mutation or post-translational modification relative to a wild type or unmodified polypeptide, respectively, the method comprising:
(a) contacting the biological sample with a hydrolyzing agent, wherein the hydrolyzing agent is capable of hydrolyzing the distinct polypeptide in a sequence-specific manner such that at least one distinct peptide comprising said mutation or post-translational modification and having a predetermined peptide measured accurate mass would result if the at least one distinct polypeptide were present in the biological sample, to obtain a hydrolyzed sample;
(b) bringing the hydrolyzed sample in contact with a substrate comprising at least one immobilized binding partner, wherein the at least one immobilized binding partner is capable of specifically binding the distinct peptide;
(c) removing the hydrolyzed sample from the substrate in a manner such that the distinct peptide would remain bound to the immobilized binding partner;
(d) contacting the substrate with an elution solution, wherein the distinct peptide would dissociate from the immobilized binding partner into the elution solution, to obtain an elution solution comprising a plurality of molecules;
(e) determining the measured accurate mass of at least one molecule present in the elution solution; and
(f) determining the presence of the at least one distinct polypeptide in the biological sample when a measured accurate mass of at least one molecule is substantially equal to the predetermined peptide measured accurate mass of the at least one distinct peptide.

2. The method of claim 1 , wherein at least one standard peptide is added to the plurality of molecules, wherein the at least one standard peptide has substantially the same amino acid sequence as the at least one distinct peptide but a different measured accurate mass.

3. The method of claim 1 , wherein at least two reference peptides are added to the plurality of molecules, wherein the at least two reference peptides have a known liquid chromatography elution order.

4. The method of claim 2 , wherein the standard peptide comprises an isotope selected from the group consisting of 15 N, 13 C, 18 O and 2 H.

5. The method of claim 2 , wherein the at least one standard peptide and the at least one distinct peptide co-segregate during liquid chromatography.

6. The method of claim 4 , wherein the presence of the at least one distinct polypeptide is confirmed by the co-segregation of the at least one standard peptide and the at least one molecule and by the difference in measured accurate mass between the at least one standard peptide and the at least one molecule.

7. The method of claim 1 , wherein the plurality of molecules are segregated during liquid chromatography according to a feature selected from the group consisting of hydrophobicity, charge, and retention time.

8. The method of claim 2 , wherein the at least one standard peptide and the at least one distinct peptide have a substantially identical retention time.

9. The method of claim 1 , wherein the mutation is an addition, deletion and/or substitution of about 1 to about 10 amino acid residues.

10. The method of claim 1 , wherein the post-translational modification is selected from the group consisting of phosphorylation, acetylation, ubiquitination, and glycosylation.

11. The method of claim 1 , wherein the biological sample is derived from saliva, mucous, tears, blood, serum, lymph fluids, buccal cells, circulating tumor cells, mucosal cells, biopsy tissue, cerebrospinal fluid, semen, feces, plasma, urine, a suspension of cells, or a suspension of cells and viruses.

12. The method of claim 1 , wherein the biological sample comprises a number of different polypeptides selected from the group consisting of between about 5,000 to about 20,000 different polypeptides, between about 7,500 to about 15,000 different polypeptides, and up to about 100,000 different polypeptides and isoforms thereof.

13. The method of claim 1 , wherein the hydrolyzing agent is selected from the group consisting of an enzyme and a chemical.

14. The method of claim 1 , wherein the hydrolyzing agent is selected from the group consisting of cyanogen bromide, BNPS-Skatole, formic acid, trypsin, Lysine-C endopeptidase (LysC); arginine-C endopeptidase (ArgC), Asp-N, glutamic acid, endopeptidase (GluC), chymotrypsin, and combinations thereof.

15. The method of claim 1 , wherein the substrate comprises a substance selected from the group consisting of a gel matrix and polymer beads.

16. The method of claim 1 , wherein the at least one immobilized binding partner comprises a reagent selected from the group consisting of an antibody or peptide binding fragment thereof, a protein that specifically binds to the distinct peptide, an antibody or antibody fragment that binds a mutant signature peptide, and an antibody or antibody fragment that binds a wild type peptide.

17. The method of claim 1 , wherein the at least one immobilized binding partner is 1 to about 500 or 1 to at least 500 immobilized binding partners, wherein each immobilized binding partner specifically binds to a different distinct peptide.

18. The method of claim 1 , wherein the determining measured accurate mass includes the step of ionization of the at least one molecule by a method selected from the group consisting of Atmospheric Pressure Chemical Ionization (APCI), Chemical Ionization (CI), Electron Impact (EI), Electrospray Ionization (ESI), Fast Atom Bombardment (FAB), Field Desorption/Field Ionization (FD/FI), Matrix Assisted Laser Desorption Ionization (MALDI), and Thermospray Ionization.

19. The method of claim 1 , wherein determining the measured accurate mass is performed using an instrument selected from the group consisting of an instrument with a mass accuracy of 5 ppm or less and an instrument with a mass accuracy of 1 ppm or less.

20. The method of claim 1 , wherein the biological sample is depleted of a protein selected from the group consisting of albumin, IgG, IgA, transferrin, haptoglobin, and anti-trypsin; or combinations thereof, prior to step (a).

Assignees

• Cell Signaling Technology Inc

Inventors

• Moritz Albrecht
• Rush Ii John Edward
• Polakiewicz Roberto

Classifications

• G01N33/6848 Primary

  Methods of protein analysis involving mass spectrometry · CPC title

• G01N30/7233

  interfaced to liquid or supercritical fluid chromatograph (interfaces in general for introducing or extracting samples to be analysed with specially adapted mass spectrometer, see H01J49/04) · CPC title

• B01D15/325

  Reversed phase · CPC title

• H01J49/00

  Particle spectrometers or separator tubes · CPC title

• G01N2560/00

  Chemical aspects of mass spectrometric analysis of biological material · CPC title