A reliable protocol for producing primary monomeric HIV-1 gp120 is presented.
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The protocol avoids renowned problems in amplifying and cloning HIV-1 Env sequences.
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The conditions for studying the gp120 interactions with CD4 and CCR5 are described.
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The binding assay to CD4 is adaptable to large collections of glycoproteins.
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The receptor binding assays confirmed that the gp120 are functionally relevant.
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