- Mechanistic insights into the enhancement of adeno-associated virus transduction by proteasome inhibitors.
Mechanistic insights into the enhancement of adeno-associated virus transduction by proteasome inhibitors.
Journal of virology (2013-09-13)
Angela M Mitchell, R Jude Samulski
PMID24027330
ZUSAMMENFASSUNG
Proteasome inhibitors (e.g., bortezomib, MG132) are known to enhance adeno-associated virus (AAV) transduction; however, whether this results from pleotropic proteasome inhibition or off-target serine and/or cysteine protease inhibition remains unresolved. Here, we examined recombinant AAV (rAAV) effects of a new proteasome inhibitor, carfilzomib, which specifically inhibits chymotrypsin-like proteasome activity and no other proteases. We determined that proteasome inhibitors act on rAAV through proteasome inhibition and not serine or cysteine protease inhibition, likely through positive changes late in transduction.
MATERIALIEN
Produktnummer
Marke
Produktbeschreibung
Sigma-Aldrich
αα-Chymotrypsin aus Rinderpankreas, Type II, lyophilized powder, ≥40 units/mg protein
Sigma-Aldrich
αα-Chymotrypsin, (TLCK treated to inactivate residual tryspin activity), Type VII, essentially salt-free, lyophilized powder, ≥40 units/mg protein
Sigma-Aldrich
αα-Chymotrypsin aus Rinderpankreas, Type I-S, essentially salt-free, lyophilized powder
Sigma-Aldrich
αα-Chymotrypsin aus Rinderpankreas, suitable for protein sequencing, salt-free, lyophilized powder
Sigma-Aldrich
α-Chymotrypsin−Agarose from bovine pancreas, lyophilized powder, 2,000-3,500 units/g agarose (One ml gel will yield 65-120 units)