Synaptotagmin and collapsin response mediator protein as biomarkers for traumatic brain injury
Collapsin response mediator proteins (CRMPs) decreased in tissue and increased in biological fluids after neural injury from traumatic brain injury (TBI). Significant decreases of CRMP1, CRMP2, CRMP4 and CRMP5 were accompanied by the appearance of distinct 58 kDa (CRMP-2) or 55 kDa (CRMP-4) breakdown products from proteolytic cleavage by calpain. Synaptotagmin breakdown products were also associated with TBI and could be detected along with intact protein in human cerebral spinal fluid (CSF). Both biomarkers were detected in human biofluid and related to recovery from traumatic brain injury.
1. A method of determining the presence of trauma induced brain injury, comprising:
collecting a biological sample from an injured subject suspected of having the trauma induced brain injury, wherein the biological sample is blood or cerebral spinal fluid (CSF);
measuring said sample for an amount of at least one biomarker of collapsin response mediator protein-1, -2, -3, -4, or -5 (CRMP), synaptotagmin or at least one CRMP breakdown product (BDP) or synaptotagmin BDP formed by the trauma induced brain injury;
comparing the amount of the biomarker CRMP or synaptotagmin with an amount of CRMP or synaptotagmin in an uninjured subject, wherein a decreased amount of the CRMP or the synaptotagmin from said injured subject compared with the uninjured subject is indicative of trauma induced brain injury in said injured subject; or
comparing the amount of the biomarker CRMP BDP or synaptotagmin BDP with an amount of the respective BDP in an uninjured subject, wherein synaptotagmin BDP is one or more proteins produced by calpain cleavage between a glycine-lysine (G-K) in the synaptotagmin and wherein the CRMP BDP is one or more proteins produced by calpain cleavage between one or more of serine-serine (S-S), Leu-Tyr (L-Y), tyrosine-aspartic (Y-D) or arginine-glycine (R-G), wherein an increased amount of the CRMP BDP or the synaptotagmin BDP, as compared with the respective amount in the uninjured subject, is indicative of the trauma induced brain injury.
2. The method of claim 1 wherein the measured CRMP is CRMP-1, CRMP-2, CRMP-4, or CRMP-5.
3. The method of claim 1 further comprising collecting successive biological samples and monitoring the amount of the biomarker measured in the biological sample of the injured subject from time of injury to a time when the amount of the biomarker measured in a successive biological samples of the injured subject substantially equals the amount of the biomarker measured in an uninjured subject, wherein recovery of the injured subject is indicated when the amount of the biomarker approaches the amount of the biomarker measured in the uninjured subject.
4. The method of claim 1 wherein the measured biomarker is the CRMP-2 with a molecular weight of 62kDa or 66kDa whereby a decrease of the biomarker in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.
5. The method of claim 1 wherein the measured biomarker is a CRMP-4 BDP with a molecular weight of 58kDa whereby an increase of the biomarker in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.
6. The method of claim 1 wherein the measured biomarker is one or more BDPs of synaptotagmin with a molecular weight of 35 kDa, 20 kDa or 46 kDa whereby an increase of the biomarker in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.
7. The method of claim 1 wherein the measured biomarker is a CRMP-2 BDP with a molecular weight of 55kDa whereby an increase of the biomarker in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.
8. The method of claim 1 wherein said sample is measured for an amount of at least two biomarkers of a collapsin response mediator protein (CRMP), synaptotagmin or a BDP of CRMP or synaptotagmin formed by the trauma induced brain injury.
9. The method of claim 8 wherein the first biomarker is a CRMP and the second biomarker is a BDP of the CRMP.
10. The method of claim 9 wherein a decreased amount of the CRMP and an increased amount of the CRMP BDP from said injured subject, as compared with the uninjured subject, is indicative of the trauma induced brain injury in said injured subject.
11. The method of claim 9 wherein the CRMP is CRMP-2 with a molecular weight of 62kDa or 66kDa and the CRMP BDP is CRMP-2 55kDa BDP whereby a decrease of CRMP-2 62 kDa or 66 kDa proteins and an increase of CRMP-2 55 kDa BDP in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.
12. The method of claim 9 wherein the CRMP is CRMP-4 with a molecular weight of 62kDa and the CRMP BDP is CRMP-2 55kDa BDP whereby a decrease of CRMP-2 62 kDa or 66 kDa proteins and an increase of CRMP-2 55 kDa BDP in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.
13. The method of claim 8 wherein the first biomarker is synaptotagmin and the second biomarker is a BDP of synaptotagmin.
14. The method of claim 13 wherein a decreased amount of the synaptotagmin and an increased amount of the synaptotagmin BDP from said injured subject, as compared with the uninjured subject, is indicative of the trauma induced brain injury in said injured subject.
15. The method of claim 14 wherein the synaptotagmin has a molecular weight of 65kDa and the synaptotagmin BDP is a 35 kDa, 20 kDa or 46 kDa BDP whereby a decrease of synaptotagmin 65kDa protein and an increase of 35 kDa, 20 kDa or 46 kDa BDP in the injured subject with respect to the uninjured subject is indicative of trauma induced brain injury.