Abstract
BackgroundPrevious studies have shown that 3-hydroxyphthalic anhydride (HP)-modified bovine milk protein, β-lactoglobulin (β-LG), is a promising microbicide candidate. However, concerns regarding the potential risk of prion contamination in bovine products and carcinogenic potential of phthalate derivatives were raised. Here we sought to replace bovine protein with an animal protein of non-bovine origin and substitute HP with another anhydride for the development of anti-HIV microbicide for preventing HIV sexual transmission.ResultsMaleic anhydride (ML), succinic anhydride (SU) and HP at different conditions and variable pH values were used for modification of proteins. All the anhydrate-modified globulin-like proteins showed potent anti-HIV activity, which is correlated with the percentage of modified lysine and arginine residues in the modified protein. We selected maleic anhydride-modified ovalbumin (ML-OVA) for further study because OVA is easier to obtain than β-LG, and ML is safer than HP. Furthermore, ML-OVA exhibited broad antiviral activities against HIV-1, HIV-2, SHIV and SIV. This modified protein has no or low in vitro cytotoxicity to human T cells and vaginal epithelial cells. It is resistant to trypsin hydrolysis, possibly because the lysine and arginine residues in OVA are modified by ML. Mechanism studies suggest that ML-OVA inhibits HIV-1 entry by targeting gp120 on HIV-1 virions and also the CD4 receptor on the host cells.ConclusionML-OVA is a potent HIV fusion/entry inhibitor with the potential to be developed as an effective, safe and inexpensive anti-HIV microbicide.
Highlights
Previous studies have shown that 3-hydroxyphthalic anhydride (HP)-modified bovine milk protein, βlactoglobulin (β-LG), is a promising microbicide candidate
We previously found that anhydrate-modified bovine proteins, especially 3hydroxyphthalic anhydride-modified bovine β-lactoglobulin (3HP-β-LG), may fulfill these requirements because they have potent antiviral activities against human immunodeficiency virus (HIV)-1, HIV-2, simian immunodeficiency viruses (SIV) and herpes simplex viruses (HSV). 3HP-β-LG is effective against some sexually transmitted infection (STI) pathogens, e.g., Chlamydia trachomatis
By evaluating the anti-HIV activities of these modifications and the characteristics of proteins used in the reaction, we found that HP-modified chicken ovalbumin (HPOVA) was the most promising anti-HIV inhibitor among these modified proteins [14]
Summary
Previous studies have shown that 3-hydroxyphthalic anhydride (HP)-modified bovine milk protein, βlactoglobulin (β-LG), is a promising microbicide candidate. We sought to replace bovine protein with an animal protein of non-bovine origin and substitute HP with another anhydride for the development of anti-HIV microbicide for preventing HIV sexual transmission. Despite extraordinary advances in the development of prevention and therapeutic strategies against human immunodeficiency virus (HIV) infection, HIV/AIDS continues to spread at an alarming rate worldwide. Unprotected sex is the primary infection route for humans, especially for females, to acquire HIV/AIDS. We previously found that anhydrate-modified bovine proteins, especially 3hydroxyphthalic anhydride-modified bovine β-lactoglobulin (3HP-β-LG), may fulfill these requirements because they have potent antiviral activities against HIV-1, HIV-2, simian immunodeficiency viruses (SIV) and herpes simplex viruses (HSV).
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