Titlebook: Subcellular Biochemistry; Volume 10 Donald B. Roodyn Book 1984 Plenum Press, New York 1984 Calcium.Chloroplast.DNA.Lipid.Nucleotide.RNA.bio

協(xié)定

stress-test

高射炮

Rafael Sentandreu,Enrique Herrero,José P. Martínez-García,Germán Larribairus. This chapter gives a general overview of how HIV-1 is neutralized by antibody, why the neutralizing antibody response fails to control infection and, finally, what is being done to develop an HIV-1 vaccine that has an effective antibody component.

Dedication

籠子

Héctor N. Seuánezypeptide composed of a C-terminal-truncated . peptide and the entire . peptide. The second stage involves the proteolytic processing of this fusion protein to generate mature structural and functional viral components (Debouck ., 1987; Lillehoj ., 1988). An HIV-specific protease cleaves the fusion p

初次登臺

oduce some ten different recombinant baculoviruses expressing various gene products encoded by both HIV-1 and HIV-2. Here we describe four of these recombinant viruses that produce products encoded by the gag and . genes of HIV-1. We show that a feature of gag and . translation in HIV-1 infected cel

發(fā)生

碎石

對手

Rafael Sentandreu,Enrique Herrero,José P. Martínez-García,Germán Larribacific antigens. Perhaps the most beneficial B cell response is one that is directed against the surface gp120 and transmembrane gp41 envelope glycoproteins of the virus; both glycoproteins are major targets for the antibody-mediated neutralization of HIV-1 infectivity. To ensure its survival, the vi

HEAVY

B. B. Biswas,B. Ghosh,Arun Lahiri Majumdercific antigens. Perhaps the most beneficial B cell response is one that is directed against the surface gp120 and transmembrane gp41 envelope glycoproteins of the virus; both glycoproteins are major targets for the antibody-mediated neutralization of HIV-1 infectivity. To ensure its survival, the vi