Method for automated, large-scale measurement of the molecular flux rates of the proteome or the organeome using mass spectrometry

Patent metadata

Field	Value
Publication number	US-8969287-B2
Application number	US-201313922207-A
Country	US
Kind code	B2
Filing date	Jun 19, 2013
Priority date	Jul 30, 2002
Publication date	Mar 3, 2015
Grant date	Mar 3, 2015

Abstract

Disclosed here is a method for measuring the kinetics (i.e., the molecular flux rates-synthesis and breakdown or removal rates) of a plurality of proteins or organic metabolites in living systems. The methods may be accomplished in a high-throughput, large-scale automated manner, by using existing mass spectrometric profiling techniques and art well known in the fields of static proteomics and static organeomics, without the need for additional biochemical preparative steps or analytic/instrumental devices.

First claim

I claim:

1. A method of determining the effect of a diagnostic or therapeutic agent on a cell, tissue or organism, said method comprising:
a) administering one or more isotope-labeled protein precursors to said cell, tissue or organism for a period of time sufficient for one or more isotope labels of the one or more isotope-labeled protein precursors to be incorporated into proteins in the cell, tissue or organism;
b) obtaining a sample from the cell, tissue, or organism wherein the sample comprises a plurality of proteins;
c) degrading the plurality of proteins to form a mixture of peptides from the plurality of proteins;
d) performing a first mass spectrometry on the mixture of peptides from the plurality of proteins to identify a plurality of mass isotopomeric envelopes of an initial series of ionic fragments representing individual proteins;
e) performing a second mass spectrometry to identify secondary fragments of the initial series of ionic fragments;
f)comparing the initial series of ionic fragments identified by the first mass spectrometry with the secondary fragments identified by the second mass spectrometry to identify one or more of the individual proteins in the sample;
g) quantifying relative and absolute mass isotopomer abundances of the ionic fragments of one or more of the identified individual proteins within the mass isotopomeric envelope;
h) calculating the molecular flux rates of one or more of the identified individual proteins;
i) administering said diagnostic or therapeutic agent to said cell, tissue or organism; and
j) calculating the molecular flux rates of one or more of the identified individual proteins according to steps a) through h) after said administering step i), wherein a difference in the molecular flux rate of one or more of the identified individual proteins before and after administration of said drug agent to said cell, tissue or organism identifies the effect of the diagnostic or therapeutic agent on the cell, tissue or organism.

2. The method of claim 1 , wherein steps a) to j) are performed in an automated high-throughput manner.

3. The method of claim 1 , wherein said administering step (a) is continuous.

4. The method of claim 1 , wherein said administering step (a) comprises administering said one or more protein precursors at regular measured intervals.

5. The method of claim 1 , wherein said one or more isotope-labeled protein precursors are administered orally.

6. The method of claim 1 , further comprising the step of displaying the molecular flux rates of one or more of the identified individual proteins of said plurality of proteins.

7. The method of claim 1 , wherein said one or more isotope-labeled protein precursors is an isotope-labeled amino acid.

8. The method of claim 1 , wherein the one or more isotope-labeled protein precursors are selected from the group consisting of isotope-labeled H 2 O, isotope-labeled CO 2 , isotope-labeled NH 3 , and isotope-labeled HCO 3 .

9. The method of claim 1 , wherein said one or more isotope labels is selected from the group consisting of 2 H, 13 C, 15 N, 18 O, 33 S and 34 S.

10. The method of claim 1 , wherein said one or more isotope label is 2 H.

11. The method of claim 1 , wherein said one or more isotope-labeled protein precursor is selected from the group consisting of 2 H 2 O, H 2 18 O, 13 CO 2 , C 18 O 17 O, H 16 CO 3 , 15 NH 3 , 2 H-labeled amino acids, 13 C-labeled amino acids, 15 N-labeled amino acids, 18 O-labeled amino acids, 34 S-labeled amino acids, and 33 S-labeled amino acids.

12. The method of claim 1 , wherein said one or more isotope-labeled protein precursor is 2 H 2 O.

13. The method of claim 1 , wherein the organism is a human.

Assignees

• Univ California

Inventors

• Hellerstein Marc K

Classifications

• G01N33/6803

  General methods of protein analysis not limited to specific proteins or families of proteins · CPC title

• G01N2500/10

  involving cells · CPC title

• G01N33/6848 Primary

  Methods of protein analysis involving mass spectrometry · CPC title

• A61K49/0002

  General or multifunctional contrast agents, e.g. chelated agents · CPC title

• G01N2458/15

  Non-radioactive isotope labels, e.g. for detection by mass spectrometry · CPC title