The overall objective of this research plan is to evaluate and optimize a new analytical procedure (MicroGravimetric ImmunoAssay) for the detection and quantitation of an important brain protein, myelin basic protein, with projected utility in the diagnosis and treatment of Multiple Sclerosis and Alzheimer's disease. We believe that the development and eventual commercialization of such a methodology could simplify and speed the diagnosis of important mental disorders. The research plan includes the construction of microelectronic sensors based on surface acoustic wave technology which incorporates a polymer layer that protects the sensor, reduces non-specific binding and allows covalent coupling of monoclonal antibodies. Prototype sensors will be tested for fundamental operational characteristics. Biochemical reagents including myelin basic protein and monoclonal antibodies to that protein will be prepared in a parallel program. When both are ready, sensors incorporating the monoclonal antibodies will be evaluated and compared to reference laboratory techniques.

Project Start
1986-04-01
Project End
1986-10-31
Budget Start
1986-04-01
Budget End
1986-10-31
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Integrated Chemical Sensors Corporation
Department
Type
DUNS #
City
Newton
State
MA
Country
United States
Zip Code
02164
Anderson, J L; Khan, M; David, W S et al. (1999) Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22. Am J Med Genet 82:161-5
Conlon, P J; Lynn, K; Winn, M P et al. (1999) Spectrum of disease in familial focal and segmental glomerulosclerosis. Kidney Int 56:1863-71
Scott, W K; Yamaoka, L H; Stajich, J M et al. (1999) The alpha-synuclein gene is not a major risk factor in familial Parkinson disease. Neurogenetics 2:191-2
Nance, M A; Raabe, W A; Midani, H et al. (1998) Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21. Hum Hered 48:169-78
Messina, D N; Speer, M C; Pericak-Vance, M A et al. (1997) Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am J Hum Genet 61:909-17
Scott, W K; Staijich, J M; Yamaoka, L H et al. (1997) Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research Group. Science 277:387-8; author reply 389