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FASEB J. 2015 Jan;29(1):70-80. doi: 10.1096/fj.14-252262. Epub 2014 Oct 28.

Structural basis of clade-specific HIV-1 neutralization by humanized anti-V3 monoclonal antibody KD-247.

Author information

1
Christopher S. Bond Life Sciences Center, Department of Molecular Microbiology and Immunology, School of Medicine.
2
Structural Biology Core, and.
3
Department of Biochemistry, University of Missouri, Columbia, Missouri, USA;
4
AIDS Research Center, National Institute of Infectious Diseases, Tokyo, Japan;
5
The Chemo-Sero-Therapeutic Research Institute (Kaketsuken), Kyokushi, Kikuchi, Kumamoto, Japan; and.
6
Division of Clinical Retrovirology and Infectious Diseases, Center for AIDS Research, Kumamoto University, Kumamoto, Japan.
7
Christopher S. Bond Life Sciences Center, Department of Molecular Microbiology and Immunology, School of Medicine, Department of Biochemistry, University of Missouri, Columbia, Missouri, USA; sarafianoss@missouri.edu.

Abstract

Humanized monoclonal antibody KD-247 targets the Gly(312)-Pro(313)-Gly(314)-Arg(315) arch of the third hypervariable (V3) loop of the HIV-1 surface glycoprotein. It potently neutralizes many HIV-1 clade B isolates, but not of other clades. To understand the molecular basis of this specificity, we solved a high-resolution (1.55 Å) crystal structure of the KD-247 antigen binding fragment and examined the potential interactions with various V3 loop targets. Unlike most antibodies, KD-247 appears to interact with its target primarily through light chain residues. Several of these interactions involve Arg(315) of the V3 loop. To evaluate the role of light chain residues in the recognition of the V3 loop, we generated 20 variants of KD-247 single-chain variable fragments with mutations in the antigen-binding site. Purified proteins were assessed for V3 loop binding using AlphaScreen technology and for HIV-1 neutralization. Our data revealed that recognition of the clade-specificity defining residue Arg(315) of the V3 loop is based on a network of interactions that involve Tyr(L32), Tyr(L92), and Asn(L27d) that directly interact with Arg(315), thus elucidating the molecular interactions of KD-247 with its V3 loop target.

KEYWORDS:

HIV; crystal structure; entry; single-chain variable fragment

PMID:
25351987
PMCID:
PMC4285544
DOI:
10.1096/fj.14-252262
[Indexed for MEDLINE]
Free PMC Article

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