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Stabilization of the gp120 V3 loop through hydrophobic interactions reduces the immunodominant V3-directed non-neutralizing response to HIV-1 envelope trimers.

Publication ,  Journal Article
de Taeye, SW; de la Peña, AT; Vecchione, A; Scutigliani, E; Sliepen, K; Burger, JA; van der Woude, P; Schorcht, A; Schermer, EE; van Gils, MJ ...
Published in: J Biol Chem
February 2, 2018

To provide protective immunity against circulating primary HIV-1 strains, a vaccine most likely has to induce broadly neutralizing antibodies to the HIV-1 envelope glycoprotein (Env) spike. Recombinant Env trimers such as the prototype BG505 SOSIP.664 that closely mimic the native Env spike can induce autologous neutralizing antibodies (NAbs) against relatively resistant (tier 2) primary viruses. Ideally, Env immunogens should present broadly neutralizing antibody epitopes but limit the presentation of immunodominant non-NAb epitopes that might induce off-target and potentially interfering responses. The V3 loop in gp120 is such a non-NAb epitope that can effectively elicit non-NAbs when animals are immunized with SOSIP.664 trimers. V3 immunogenicity can be diminished, but not abolished, by reducing the conformational flexibility of trimers via targeted sequence changes, including an A316W substitution in V3, that create the SOSIP.v4.1 and SOSIP.v5.2 variants. Here, we further modified these trimer designs by introducing leucine residues at V3 positions 306 and 308 to create hydrophobic interactions with the tryptophan residue at position 316 and with other topologically proximal sites in the V1V2 domain. Together, these modifications further stabilized the resulting SOSIP.v5.2 S306L/R308L trimers in the prefusion state in which V3 is sequestered. When we tested these trimers as immunogens in rabbits, the induction of V3 non-NAbs was significantly reduced compared with the SOSIP.v5.2 trimers and even more so compared with the SOSIP.664 prototype, without affecting the autologous NAb response. Hence, these additional trimer sequence modifications may be beneficial for immunization strategies that seek to minimize off-target non-NAb responses.

Duke Scholars

Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

February 2, 2018

Volume

293

Issue

5

Start / End Page

1688 / 1701

Location

United States

Related Subject Headings

  • Protein Stability
  • Protein Multimerization
  • Hydrophobic and Hydrophilic Interactions
  • Humans
  • HIV Envelope Protein gp120
  • HIV Antibodies
  • HEK293 Cells
  • Epitopes
  • Biochemistry & Molecular Biology
  • Antibodies, Neutralizing
 

Citation

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de Taeye, S. W., de la Peña, A. T., Vecchione, A., Scutigliani, E., Sliepen, K., Burger, J. A., … Sanders, R. W. (2018). Stabilization of the gp120 V3 loop through hydrophobic interactions reduces the immunodominant V3-directed non-neutralizing response to HIV-1 envelope trimers. J Biol Chem, 293(5), 1688–1701. https://doi.org/10.1074/jbc.RA117.000709
Taeye, Steven W. de, Alba Torrents de la Peña, Andrea Vecchione, Enzo Scutigliani, Kwinten Sliepen, Judith A. Burger, Patricia van der Woude, et al. “Stabilization of the gp120 V3 loop through hydrophobic interactions reduces the immunodominant V3-directed non-neutralizing response to HIV-1 envelope trimers.J Biol Chem 293, no. 5 (February 2, 2018): 1688–1701. https://doi.org/10.1074/jbc.RA117.000709.
de Taeye SW, de la Peña AT, Vecchione A, Scutigliani E, Sliepen K, Burger JA, et al. Stabilization of the gp120 V3 loop through hydrophobic interactions reduces the immunodominant V3-directed non-neutralizing response to HIV-1 envelope trimers. J Biol Chem. 2018 Feb 2;293(5):1688–701.
de Taeye, Steven W., et al. “Stabilization of the gp120 V3 loop through hydrophobic interactions reduces the immunodominant V3-directed non-neutralizing response to HIV-1 envelope trimers.J Biol Chem, vol. 293, no. 5, Feb. 2018, pp. 1688–701. Pubmed, doi:10.1074/jbc.RA117.000709.
de Taeye SW, de la Peña AT, Vecchione A, Scutigliani E, Sliepen K, Burger JA, van der Woude P, Schorcht A, Schermer EE, van Gils MJ, LaBranche CC, Montefiori DC, Wilson IA, Moore JP, Ward AB, Sanders RW. Stabilization of the gp120 V3 loop through hydrophobic interactions reduces the immunodominant V3-directed non-neutralizing response to HIV-1 envelope trimers. J Biol Chem. 2018 Feb 2;293(5):1688–1701.

Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

February 2, 2018

Volume

293

Issue

5

Start / End Page

1688 / 1701

Location

United States

Related Subject Headings

  • Protein Stability
  • Protein Multimerization
  • Hydrophobic and Hydrophilic Interactions
  • Humans
  • HIV Envelope Protein gp120
  • HIV Antibodies
  • HEK293 Cells
  • Epitopes
  • Biochemistry & Molecular Biology
  • Antibodies, Neutralizing