Proteolytic biomarkers for traumatic injury to the nervous system
View Patent ↗The present invention identifies biomarkers that are diagnostic of nerve cell injury, organ injury, and/or neuronal disorders. Detection of different biomarkers of the invention are also diagnostic of the degree of severity of nerve injury, the cell(s) involved in the injury, and the subcellular localization of the injury.
1. A method of determining the presence of neural injury in a subject, comprising detecting at least one or more proteolytic breakdown products of microtubule-associated protein (MAP), wherein the MAP protein is MAP-1, MAP-2A, MAP-2B, MAP-2C, MAP-2D, MAP-3 or MAP-4 in a tissue or fluid sample in contact with injured neural tissue wherein a detectable, amount of the at least one or more breakdown products of MAP is indicative of neural injury in said subject when said amount is greater than in normal subjects without neural injury.
2. The method of claim 1 , wherein the MAP protein is MAP-2A, MAP-2B, MAP-2C, or MAP-2D.
3. The method of claim 1 , wherein the breakdown product is a cleavage product of SEQ ID NO:10.
4. The method of claim 3 , wherein the cleavage product is between position 99 and 100 of SEQ ID NO: 10.
5. The method of claim 1 , wherein the neural injury is traumatic brain injury (TBI).
6. The method of claim 1 , wherein the fluid sample is cerebrospinal fluid (CSF) or blood.
7. The method of claim 1 , wherein the tissue sample is cortical tissue from the hippocampus.
8. The method of claim 1 , wherein the breakdown products of MAP are detected using an immunoassay.
9. The method of claim 1 , wherein the breakdown products of MAP are detected using a biochip array.
10. The method of claim 9 , wherein the biochip array is a protein chip array.
11. The method of claim 9 , wherein the biochip array is a nucleic acid array.
12. The method of claim 1 , wherein the breakdown products of MAP are immobilized on the biochip array.
13. The method of claim 12 , wherein the immobilized breakdown products are subjected to laser ionization to detect the molecular weight of the markers.
14. The method of claim 13 , wherein ille molecular weight of the one or more breakdown products is analyzed against a threshold intensity that is normalized against total ion current.
15. The method of claim 14 , wherein logarithmic transformation is used for reducing peak intensity ranges to limit the number or breakdown products detected.