Organic non-sugar compounds for protection of biologically active molecules and conjugate labels and methods of use thereof
View Patent ↗Provided are methods comprising the use of non-sugar organic compatible solutes for protection and preservation of the activity of biologically active molecules and conjugate labels. The methods are particularly adaptable for use in conjunction with immunoassays, such as for example, immunochromatographic test assays and may be incorporated into any test methodology wherein a dry test strip is used as a carrier for depositing, mobilizeable and/or immobilized biologically active molecules and/or conjugate labels.
1. A method for preserving the activity of one or more biologically active molecules in a dried and reconstituted state, comprising:
a) depositing the one or more biologically active molecules onto a surface;
b) depositing one or more non-sugar organic compatible solutes onto the surface, wherein said one or more non-sugar organic compatible solutes are each selected from the group consisting of: glycine, alanine, serine, proline, sodium glutamate, lysine, aminobutric acid, taurine, amines, betaine, sarcosine, trimethylamine N-oxide, 2-Naphthol, ectoine, hydroxyectoine, glycerine, deoxyribonucleic acid, adenosine monophosphate, PCR primers, spermine, spermidine, polyethyleneimine, polyhystidine, polythymadilic acid, acetyl-L-camitine, and L-citruline; and
c) drying the deposited one or more biologically active molecules and the deposited one or more non-sugar organic compatible solutes on the surface, wherein the one or more non-sugar organic compatible solutes preserves the activity of the one or more biologically active molecules in the dried and reconstituted state.
2. The method of claim 1 , wherein the one or more biologically active molecules and the one or more non-sugar organic compatible solutes are deposited onto said surface concurrently.
3. The method of claim 2 , wherein each of the one or more biologically active molecules are selected from the group consisting of: an antibody, a labeled antibody, an antibody fragment and a labeled antibody fragment, and the one or more non-sugar organic compatible solutes comprise single amino acids.
4. The method of claim 2 , wherein the one or more biologically active molecules are selected from the group consisting of: an antibody, a labeled antibody, an antibody fragment and a labeled antibody fragment, and the one or more non-sugar organic compatible solutes comprise single amino acid chains of about 1 to about 10 amino acids.
5. The method of claim 3 , wherein each of the one or more biologically active molecules are selected from the group consisting of: an immobilized antibody, an immobilized antibody fragment, a mobilizable labeled antibody and a mobilizable labeled antibody fragment, and the surface comprises a portion of a test strip.
6. The method of claim 5 , wherein the test strip is immunochromatographic.
7. The method of claim 5 , wherein the portion of the test strip is a conjugate pad.
8. The method of claim 5 , wherein the portion of the test strip is a detection zone.
9. The method of claim 5 , wherein said immunochromatographic strip comprises a lateral flow device.
10. The method of claim 2 , wherein said one or more biologically active molecules are selected from the group consisting of: an antibody, a labeled antibody, an antibody fragment and a labeled antibody fragment, and said one or more non-sugar organic compatible solutes comprise one or more amines.
11. The method of claim 2 , wherein said one or more biologically active molecules are selected from the group consisting of: an antibody, a labeled antibody, an antibody fragment and a labeled antibody fragment, and said one or more non-sugar organic compatible solutes comprise osmolytes or other compatible solutes.
12. A method for preserving the activity of one or more biologically active molecules in a dried and reconstituted state, comprising:
a) providing a sample;
b) providing a test strip with at least a portion comprising the one or more biologically active molecules and one or more non-sugar organic compatible solutes, wherein said one or more non-sugar organic compatible solutes protects and preserves the activity of said one or more biologically active molecules in the dried and reconstituted state, wherein said one or more non-sugar organic compatible solutes are each selected from the group consisting of: glycine, alanine, serine, proline, sodium glutamate, lysine, aminobutric acid, taurine, amines, betaine, sarcosine, trimethylamine N-oxide, 2-Naphthol, ectoine, hydroxyectoine, glycerine, deoxyribonucleic acid, adenosine monophosphate, PCR primers, spermine, spermidine, polyethyleneimine, polyhystidine, polythymadilic acid, acetyl-L-camitine, and L-citruline;
c) contacting said with said test strip; and
d) detecting the presence of or measuring the amount of an analyte in the sample, wherein said one or more non-sugar organic compatible solutes protects and preserves the activity of said one or more biologically active molecules in the dried and reconstituted state.
13. The method of claim 12 , wherein the portion of the test strip is a conjugate pad.
14. The method of claim 12 , wherein the portion of the test strip is a detection zone.
15. The method of claim 12 , wherein the test strip is immunochromatographic.
16. The method of claim 12 , wherein the test strip comprises a lateral flow device.
17. A test strip defining a flow path and comprising:
a porous member comprising, in dry form:
a labeled binding reagent configured to bind an analyte, and
at least one non-sugar organic compatible solute,
a porous strip separate from and in fluid contact with the porous member, the porous strip comprising a detection zone, and
a binding reagent disposed along the flow path and configured to bind the analyte and/or a complex of the analyte and the labeled binding reagent:
wherein, the binding reagent is configured to capture the analyte and/or the complex of the analyte and the labeled binding reagent in the detection zone upon the mobilization of the labeled binding reagent by a liquid comprising the analyte, and the non-sugar organic compatible solute is selected from the group consisting of glycine, alanine, serine, proline, sodium glutamate, lysine, aminobutric acid, taurine, amines, betaine, sarcosine, trimethylamine N-oxide, 2-Naphthol, ectoine, hydroxyectoine, glycerine, deoxyribonucleic acid, adenosine monophosphate, PCR primers, spermine, spermidine, polyethyleneimine, polyhystidine, polythymadilic acid, acetyl-L-camitine, and L-citruline.