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Interaction of polylysine-[HAV-VP3 peptide] constructs with DPPC mono and bilayers

✍ Scribed by P. Sospedra; I. B. Nagy; I. Haro; C. Mestres; F. Hudecz; F. Reig


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
45 KB
Volume
13
Category
Article
ISSN
0269-3879

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πŸ“œ SIMILAR VOLUMES


Interaction with Phospholipid Mono- and
✍ M. Garcia; M. Pujol; F. Reig; M. A. Alsina; I. Haro πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 214 KB

Figure 1. Pressure increases recorded after injection of (a) VP3 (102-121); (b) palmitoyl-VP3 (102-121); (c) reference MLV liposomes/VP3 (102-121) entrapped into MLV liposomes; (d) reference MLV liposomes/ palmitoyl-VP3 (102-121) incorporated into MLV liposomes under DPPC monolayers spread at 5, 10,

Interaction of VP3(110–121) Peptide with
✍ P. Sospedra; M.A. Alsina; I. Haro; C. Mestres; M.A. Busquets πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 English βš– 159 KB

The use of synthetic peptides in the goal of developing a new, inexpensive vaccine against hepatitis A virus is one of the encouraging approaches followed by many laboratories. These peptides have to be well characterized, being their physicochemical properties one of the most relevant points to con