Method and apparatus for measuring protein post-translational modification
The present invention includes a method for analyzing reactions. The method includes the steps of providing a solution of at least one acceptor chemical and at least one donor chemical. The donor chemical is capable of donating a chemical moiety to the acceptor chemical. The solution further includes at least one controller chemical that affects the reaction between the donor chemical and the acceptor chemical. The solution is then incubated so that a portion of the acceptor chemical reacts with the donor chemical to form an acceptor product. Unreacted donor chemical is separated from the acceptor product. The acceptor product or the donor chemical is then measured using X-ray fluorescence. Another aspect of the present invention includes a method for analyzing protein function. The method includes the steps of providing a solution of at least one acceptor chemical and at least one donor chemical. The donor chemical is capable of donating a chemical moiety to the acceptor chemical. The donor chemical includes a functional group selected from ester, anhydride, imide, acyl halide, and amide. The solution is then incubated so that a portion of the acceptor chemical reacts with the donor chemical to form an acceptor product. Unreacted donor chemical is separated from the acceptor product. The acceptor product or the donor chemical is then measured using X-ray fluorescence. Yet another aspect of the present invention includes a method for analyzing protein function. The method includes the steps of providing a solution of at least one acceptor chemical and at least one donor chemical. The solution is then incubated so that a portion of the acceptor chemical reacts with the donor chemical to form an acceptor product. Unreacted donor chemical is separated from the acceptor product. The acceptor product or the donor chemical is then measured using X-ray fluorescence. An additional analytical method is also used to measure either the acceptor product or the donor chemical.
1. A method for analyzing chemical reactions, comprising:
(a) providing a solution comprising solvent, at least one acceptor chemical and at least one donor chemical, Wherein the donor chemical is capable of donating a chemical moiety comprising a chemical element to the acceptor chemical, and one or more controller chemicals capable of affecting the reaction between the donor chemical and the acceptor chemical;
(b) incubating the solution to allow a portion of the acceptor chemical to react with the donor chemical to form an acceptor product;
(c) separating at least a portion of the unreacted donor chemical from the acceptor product;
(d) removing at least a portion of the solvent; and
(e) after removing the at least portion of the solvent, measuring using x-ray fluorescence at least one of the acceptor product or the donor chemical, wherein:
wherein the one or more controller chemicals includes at least one polynucleotide.
2. The method of claim 1 , wherein the step of removing at least a portion of the solvent is performed using reduced pressure.
3. The method of claim 1 , wherein at least 80% of the solvent is removed.
4. The method of claim 3 , wherein the step of separating at least a portion of the unreacted donor chemical from the acceptor product is performed using chromatography.
5. The method of claim 3 , wherein the step of separating at least a portion of the unreacted donor chemical from the acceptor product is performed using a centrifuge.
6. The method of claim 3 , wherein the step of separating at least a portion of the unreacted donor chemical from the acceptor product is performed using size exclusion chromatography.
7. The method of claim 1 , wherein the donor chemical has a concentration of less than about 100 millimolar.
8. The method of claim 1 , wherein the donor chemical and the acceptor product differ in their molecular weights by at a factor of least 10.
9. The method of claim 1 , wherein the donor chemical and the acceptor product differ in their molecular weights by a factor of at least 20.
10. The method of claim 1 , wherein the donor chemical and the acceptor product differ in their water-octanol partition coefficients by a factor of at least 10.
11. The method of claim 1 , wherein the donor chemical and the acceptor product differ in their water-octanol partition coefficients by a factor of at least 100.
12. The method of claim 1 , wherein the reaction between the donor chemical and the acceptor chemical forms at least one chemical bond.
13. The method of claim 1 , wherein the reaction between the donor chemical and the acceptor chemical breaks at least one chemical bond.
14. The method of claim 1 , wherein the donor chemical reacts with the acceptor chemical to form an acceptor product, wherein the element to be donated is selected from the group consisting of sulfur; phosphorus; selenium; chlorine; bromine; iodine; functional groups comprising at least one of sulfur, phosphorus, selenium, chlorine, bromine, and iodine; and combinations thereof.
15. The method of claim 1 , wherein the donor chemical reacts with the acceptor chemical to form an acceptor product, wherein the element to be donated is phosphorus, a functional group comprising at least one phosphorus, or a combination thereof.
16. The method of claim 1 , wherein a portion of the solvent is removed prior to measuring using x-ray fluorescence at least one of the chemicals selected from the list of acceptor product and the donor chemical.
17. The method of claim 1 wherein the sample of donor chemical or acceptor product that is subjected to x-ray fluorescence measurement is concentrated such that the area containing more than 50% of the sample based on the total amount of the sample, of donor chemical or acceptor product that is subjected to x-ray fluorescence measurement is less than 0.005 square centimeters.