Antiviral Effects of Milk Proteins: Acylation Results in Polyanionic Compounds with Potent Activity against Human Immunodeficiency Virus Types 1 and 2 in Vitro

PJ Swart, ME Kuipers, C Smit, R Pauwels… - AIDS research and …, 1996 - liebertpub.com
PJ Swart, ME Kuipers, C Smit, R Pauwels, MP De Béthune, E De Clercq, DKF Meijer
AIDS research and human retroviruses, 1996liebertpub.com
ABSTRACT A number of native and modified milk proteins from bovine or human sources
were analyzed for their inhibitory effects on human immunodeficiency virus type 1 (HIV-1)
and HIV-2 in vitro in an MT4 cell test system. The proteins investigated were lactoferrin, α-
lactalbumin, β-lactoglobulin A, and β-lactoglobulin B. By acylation of the amino function of
the lysine residues in the proteins, using anhydrides of succinic acid or cis-aconitic acid,
protein derivatives were obtained that all showed a strong antiviral activity against human …
Abstract
A number of native and modified milk proteins from bovine or human sources were analyzed for their inhibitory effects on human immunodeficiency virus type 1 (HIV-1) and HIV-2 in vitro in an MT4 cell test system. The proteins investigated were lactoferrin, α-lactalbumin, β-lactoglobulin A, and β-lactoglobulin B.
By acylation of the amino function of the lysine residues in the proteins, using anhydrides of succinic acid or cis-aconitic acid, protein derivatives were obtained that all showed a strong antiviral activity against human immunodeficiency virus type 1 and/or 2. The in vitro IC50 values of the aconitylated proteins were in the concentration range of 0.3 to 3 nM. Succinylation or aconitylation of α-lactalbumin and β-lactoglobulin A/B also produced strong anti-HIV-2 activity with IC50 values on the order 500 to 3000 nM. All compounds showed virtually no cytotoxicity at the concentration used.
Peptide-scanning studies indicated that the native lactoferrin as well as the charged modified proteins strongly bind to the V3 loop of the gp120 envelope protein, with Kd values in the same concentration range as the above-mentioned IC50. Therefore, shielding of this domain, resulting in inhibition of virus-cell fusion and entry of the virus into MT4 cells, may be the likely underlying mechanism of antiviral action.
Mary Ann Liebert