The University of Southampton
University of Southampton Institutional Repository

Engineering and characterization of a fluorescent native-like HIV-1 envelope glycoprotein Trimer

Engineering and characterization of a fluorescent native-like HIV-1 envelope glycoprotein Trimer
Engineering and characterization of a fluorescent native-like HIV-1 envelope glycoprotein Trimer

Generation of a stable, soluble mimic of the HIV-1 envelope glycoprotein (Env) trimer on the virion surface has been considered an important first step for developing a successful HIV-1 vaccine. Recently, a soluble native-like Env trimer (BG505 SOSIP.664) has been described. This protein has facilitated major advances in the HIV-1 vaccine field, since it was the first Env immunogen that induced consistent neutralizing antibodies against a neutralization-resistant (tier 2) virus. Moreover, BG505 SOSIP.664 enabled elucidation of the atomic resolution structure of the Env trimer and facilitated the isolation and characterization of new broadly neutralizing antibodies against HIV-1. Here, we designed and characterized the BG505 SOSIP.664 trimer fused to fluorescent superfolder GFP (sfGFP), a GFP variant that allows efficient folding (BG505 SOSIP.664-sfGFP). Despite the presence of the sfGFP, the Env protein largely retained its morphology, antigenicity, glycan composition, and thermostability. In addition, we show that BG505 SOSIP.664-sfGFP can be used for fluorescence-based assays, such as flow cytometry.

Green fluorescent protein (GFP), HIV-1 Env, Protein engineering, SOSIP, Superfolder GFP
2919-2934
Sliepen, Kwinten
d2551fe9-7d04-459e-85b5-29fc4b35317a
Van Montfort, Thijs
1388f4c7-5c6c-4699-bd59-1845d235eabb
Ozorowski, Gabriel
9d448a80-7310-4b30-ba44-ee8b18222a02
Pritchard, Laura K.
bfa1d1b4-50b6-401f-b153-8c3322b2e726
Crispin, Max
cd980957-0943-4b89-b2b2-710f01f33bc9
Ward, Andrew B.
78ce5b6a-b852-4ee4-a950-f7ff7b183d83
Sanders, Rogier W.
d3b67c2c-c725-42e7-b972-50b30be67c74
Sliepen, Kwinten
d2551fe9-7d04-459e-85b5-29fc4b35317a
Van Montfort, Thijs
1388f4c7-5c6c-4699-bd59-1845d235eabb
Ozorowski, Gabriel
9d448a80-7310-4b30-ba44-ee8b18222a02
Pritchard, Laura K.
bfa1d1b4-50b6-401f-b153-8c3322b2e726
Crispin, Max
cd980957-0943-4b89-b2b2-710f01f33bc9
Ward, Andrew B.
78ce5b6a-b852-4ee4-a950-f7ff7b183d83
Sanders, Rogier W.
d3b67c2c-c725-42e7-b972-50b30be67c74

Sliepen, Kwinten, Van Montfort, Thijs, Ozorowski, Gabriel, Pritchard, Laura K., Crispin, Max, Ward, Andrew B. and Sanders, Rogier W. (2015) Engineering and characterization of a fluorescent native-like HIV-1 envelope glycoprotein Trimer. Biomolecules, 5 (4), 2919-2934, [A29]. (doi:10.3390/biom5042919).

Record type: Article

Abstract

Generation of a stable, soluble mimic of the HIV-1 envelope glycoprotein (Env) trimer on the virion surface has been considered an important first step for developing a successful HIV-1 vaccine. Recently, a soluble native-like Env trimer (BG505 SOSIP.664) has been described. This protein has facilitated major advances in the HIV-1 vaccine field, since it was the first Env immunogen that induced consistent neutralizing antibodies against a neutralization-resistant (tier 2) virus. Moreover, BG505 SOSIP.664 enabled elucidation of the atomic resolution structure of the Env trimer and facilitated the isolation and characterization of new broadly neutralizing antibodies against HIV-1. Here, we designed and characterized the BG505 SOSIP.664 trimer fused to fluorescent superfolder GFP (sfGFP), a GFP variant that allows efficient folding (BG505 SOSIP.664-sfGFP). Despite the presence of the sfGFP, the Env protein largely retained its morphology, antigenicity, glycan composition, and thermostability. In addition, we show that BG505 SOSIP.664-sfGFP can be used for fluorescence-based assays, such as flow cytometry.

This record has no associated files available for download.

More information

Accepted/In Press date: 15 October 2015
Published date: October 2015
Keywords: Green fluorescent protein (GFP), HIV-1 Env, Protein engineering, SOSIP, Superfolder GFP

Identifiers

Local EPrints ID: 414312
URI: http://eprints.soton.ac.uk/id/eprint/414312
PURE UUID: 2e47e977-8b9a-40ff-94f7-fe6ad26befdb
ORCID for Max Crispin: ORCID iD orcid.org/0000-0002-1072-2694

Catalogue record

Date deposited: 26 Sep 2017 16:30
Last modified: 11 Jul 2024 01:58

Export record

Altmetrics

Contributors

Author: Kwinten Sliepen
Author: Thijs Van Montfort
Author: Gabriel Ozorowski
Author: Laura K. Pritchard
Author: Max Crispin ORCID iD
Author: Andrew B. Ward
Author: Rogier W. Sanders

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×