TY - JOUR
T1 - Gold manno-Glyconanoparticles for Intervening in HIV gp120 Carbohydrate-Mediated Processes
AU - Di Gianvincenzo, Paolo
AU - Chiodo, Fabrizio
AU - Marradi, Marco
AU - Penadés, Soledad
PY - 2012/5/14
Y1 - 2012/5/14
N2 - After nearly three decades since the discovery of human immunodeficiency virus (HIV) (1983), no effective vaccine or microbicide is available, and the virus continues to infect millions of people worldwide each year. HIV antiretroviral drugs reduce the death rate and improve the quality of life in infected patients, but they are not able to completely remove HIV from the body. The glycoprotein gp120, part of the envelope glycoprotein (Env) of HIV, is responsible for virus entry and infection of host cells. High-mannose type glycans that decorate gp120 are involved in different carbohydrate-mediated HIV binding. We have demonstrated that oligomannoside-coated gold nanoparticles (manno-GNPs) are able to interfere with HIV high-mannose glycan-mediated processes. In this chapter, we describe the methods for the preparation and characterization of manno-GNPs and the experiments performed by means of SPR and STD-NMR techniques to evaluate the ability of manno-GNPs to inhibit 2G12 antibody binding to gp120. The antibody 2G12-mediated HIV neutralization and the lectin DC-SIGN-mediated HIV trans-infection in cellular systems are also described.
AB - After nearly three decades since the discovery of human immunodeficiency virus (HIV) (1983), no effective vaccine or microbicide is available, and the virus continues to infect millions of people worldwide each year. HIV antiretroviral drugs reduce the death rate and improve the quality of life in infected patients, but they are not able to completely remove HIV from the body. The glycoprotein gp120, part of the envelope glycoprotein (Env) of HIV, is responsible for virus entry and infection of host cells. High-mannose type glycans that decorate gp120 are involved in different carbohydrate-mediated HIV binding. We have demonstrated that oligomannoside-coated gold nanoparticles (manno-GNPs) are able to interfere with HIV high-mannose glycan-mediated processes. In this chapter, we describe the methods for the preparation and characterization of manno-GNPs and the experiments performed by means of SPR and STD-NMR techniques to evaluate the ability of manno-GNPs to inhibit 2G12 antibody binding to gp120. The antibody 2G12-mediated HIV neutralization and the lectin DC-SIGN-mediated HIV trans-infection in cellular systems are also described.
KW - Antibody 2G12
KW - Carbohydrate-mediated interactions
KW - Glycoconjugates
KW - Gold nanoparticles
KW - HIV gp120
KW - Lectin DC-SIGN
KW - Oligomannosides
KW - Saturation transfer difference-NMR
KW - Surface plasmon resonance
KW - Trans-infection assays
UR - http://www.scopus.com/inward/record.url?scp=84860720748&partnerID=8YFLogxK
U2 - 10.1016/B978-0-12-391858-1.00002-2
DO - 10.1016/B978-0-12-391858-1.00002-2
M3 - Article
C2 - 22568899
AN - SCOPUS:84860720748
VL - 509
SP - 21
EP - 40
JO - Methods in Enzymology
JF - Methods in Enzymology
SN - 0076-6879
ER -