Histidines in the Octapeptide Repeat of PrPC React with PrPSc at an Acidic pH
| Autor: | Justin T. Cruite, Laura Solforosi, Gil C. Abalos, Anne Bellon |
|---|---|
| Rok vydání: | 2011 |
| Předmět: |
Repetitive Sequences
Amino Acid PrPSc Proteins Endosome animal diseases Biochemistry Cell Line Mice Recombinant antibodies Animals Humans Histidine PrPC Proteins Neutral ph Alanine biology Chemistry Hydrogen-Ion Concentration In vitro nervous system diseases nervous system biology.protein Antibody Acids Oligopeptides |
| Zdroj: | Biochemistry. 50:1618-1623 |
| ISSN: | 1520-4995 0006-2960 |
| DOI: | 10.1021/bi1017683 |
| Popis: | Cellular PrP is actively cycled between the cell surface and the endosomal pathway. The exact site and mechanism of conversion from PrP(C) to PrP(Sc) remain unknown. We have previously used recombinant antibodies containing grafts of PrP sequence to identify three regions of PrP(C) (aa23-27, 98-110, and 136-158) that react with PrP(Sc) at neutral pH. To determine if any regions of PrP(C) react with PrP(Sc) at an acidic pH similar to that of an endosomal compartment, we tested our panel of grafted antibodies for the ability to precipitate PrP(Sc) in a range of pH conditions. At pH near or lower than 6, PrP-grafted antibodies representing the octapeptide repeat react strongly with PrP(Sc) but not PrP(C). Modified grafts in which the histidines of the octarepeat were replaced with alanines did not react with PrP(Sc). PrP(Sc) precipitated by the octapeptide at pH 5.7 was able to seed conversion of normal PrP to PrP(Sc) in vitro. However, modified PrP containing histidine to alanine substitutions within the octapeptide repeats was still converted to PrP(Sc) in N2a cells. These results suggest that once PrP has entered the endosomal pathway, the acidic environment facilitates the binding of PrP(Sc) to the octarepeat of PrP(C) by the change in charge of the histidines within the octarepeat. |
| Databáze: | OpenAIRE |
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