Resumen
In order to develop transgenic animal models that selectively overexpress various Aβ peptides, we have developed a novel expression system that selectively expresses Aβ40 or Aβ42 in the secretory pathway. This system utilizes fusion constructs in which the sequence encoding the 23-amino-acid ABri peptide at the carboxyl terminus of the 266-amino-acid type 2 transmembrane protein BRI is replaced with a sequence encoding either Aβ40 or Aβ42. Constitutive processing of the resultant BRI-Aβ fusion proteins in transfected cells results in high-level expression and secretion of the encoded Aβ peptide. Significantly, expression of Aβ42 from the BRI-Aβ42 construct resulted in no increase in secreted Aβ40, suggesting that the majority of Aβ42 is not trimmed by carboxypeptidase to Aβ40 in the secretory pathway.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 58-62 |
| Número de páginas | 5 |
| Publicación | Biochimica et Biophysica Acta - Molecular Basis of Disease |
| Volumen | 1537 |
| N.º | 1 |
| DOI | |
| Estado | Published - jul 27 2001 |
Nota bibliográfica
Funding Information:This work was supported by a Beeson Award from AFAR, an Ellison Medical Foundation New Scholars award and the NIH (NS39072, T.E.G.) (AG10491, R.W.) (Mayo Clinic ADRC, J.H.). BC05, BAN50, and BA27 were gifts of Takeda Industries.
Financiación
This work was supported by a Beeson Award from AFAR, an Ellison Medical Foundation New Scholars award and the NIH (NS39072, T.E.G.) (AG10491, R.W.) (Mayo Clinic ADRC, J.H.). BC05, BAN50, and BA27 were gifts of Takeda Industries.
| Financiadores | Número del financiador |
|---|---|
| National Institutes of Health (NIH) | AG10491 |
| National Institute of Neurological Disorders and Stroke | R01NS039072 |
| Ellison Medical Foundation | |
| Mayo Clinic Rochester | |
| American Federation for Aging Research |
ASJC Scopus subject areas
- Molecular Medicine
- Molecular Biology