• Keine Ergebnisse gefunden

Fd virus

N/A
N/A
Protected

Academic year: 2022

Aktie "Fd virus"

Copied!
1
0
0

Wird geladen.... (Jetzt Volltext ansehen)

Volltext

(1)

Fd virus

Length: 880 nm Width : 6.6 nm

Persistence length : ca. 2.8 µm Mol. Weight : 16.4x10g/mol I.E.P. : pH 4.2

The virus consists of a single­stranded circular DNA molecule coated with a protein layer of 2700 identical protein subunits. These subunits with a molecular mass of 5240 form about 99%

of the total protein mass. The rest of the protein mass belongs to the minor coat protein of 42200 daltons. The virus was originally isolated from sewageand can be grown in male strains of Escherichia coli. A review on the phase behavior and with many general references can be found in ref. 2.

References

1) D.A. Marvin and H. Hoffmann­Berling, Nature 197, 517 (1963).

2) S. Fraden, Phase transitions in colloidal suspensions of virus particles, p. 113­164 in

“Obs ervation, prediction and simulation of phase transitions in complex fluids” ( M. Baus, L.F.

Rull and J.P. Ryckaert, Eds.) Kluwer Academic Publishers, Dordrecht 1995, NATO­ASI – Series C, vol. 460.

Referenzen

ÄHNLICHE DOKUMENTE

The role of antibody polyspecificity and lipid reactivity in binding of broadly neutralizing anti-HIV-1 envelope human monoclonal antibodies 2F5 and 4E10 to glycoprotein 41

Studies on the cell-entry mechanisms of cell-penetrating peptides have revealed the very high complexity of the internalization process. Several pathways of cellular uptake are

Cell separation, the degradation of the septum after cytokinesis, requires the transcription of genes controlled by the Ace2 transcription factor (28. Cbk1

For each seed protein, we use a simulation-based approach to infer its traceability, TI(t), that is defined on the interval [0, 1]. From its traceability graph and the

A similar observation was made when the G gene was deleted from HRSV and BRSV (Karger et al., 2001; Techaarpornkul et al., 2002). When the GAG dependence of a recombinant virus with

The aim of the current study was to characterize the role of the surface protein S of coronaviruses for virus entry using the following model systems: (a) severe acute

High-resolution epitope mapping for monoclonal antibodies to the structural protein Erns of classical swine fever virus using peptide array and random peptide phage

By tryptic peptide analysis and by in vitro translation studies it has been shown that VP2 and VP3 are unrelated t o VP1 but closely related to each other In this study