Eliminating antibody polyreactivity through addition of N‐linked glycosylation. (12th May 2015)
- Record Type:
- Journal Article
- Title:
- Eliminating antibody polyreactivity through addition of N‐linked glycosylation. (12th May 2015)
- Main Title:
- Eliminating antibody polyreactivity through addition of N‐linked glycosylation
- Authors:
- Chuang, Gwo‐Yu
Zhang, Baoshan
McKee, Krisha
O'Dell, Sijy
Kwon, Young Do
Zhou, Tongqing
Blinn, Julie
Lloyd, Krissey
Parks, Robert
Von Holle, Tarra
Ko, Sung‐Youl
Kong, Wing‐Pui
Pegu, Amarendra
Wang, Keyun
Baruah, Kavitha
Crispin, Max
Mascola, John R.
Moody, M. Anthony
Haynes, Barton F.
Georgiev, Ivelin S.
Kwong, Peter D. - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Antibody polyreactivity can be an obstacle to translating a candidate antibody into a clinical product. Standard tests such as antibody binding to cardiolipin, HEp‐2 cells, or nuclear antigens provide measures of polyreactivity, but its causes and the means to resolve are often unclear. Here we present a method for eliminating antibody polyreactivity through the computational design and genetic addition of <italic>N</italic>‐linked glycosylation near known sites of polyreactivity. We used the HIV‐1‐neutralizing antibody, VRC07, as a test case, since efforts to increase VRC07 potency at three spatially distinct sites resulted in enhanced polyreactivity. The addition of <italic>N</italic>‐linked glycans proximal to the polyreactivity‐enhancing mutations at each of the spatially distinct sites resulted in reduced antibody polyreactivity as measured by (i) anti‐cardiolipin ELISA, (ii) Luminex AtheNA Multi‐Lyte ANA binding, and (iii) HEp‐2 cell staining. The reduced polyreactivity trended with increased antibody concentration over time in mice, but not with improved overall protein stability as measured by differential scanning calorimetry. Moreover, glycan proximity to the site of polyreactivity appeared to be a critical factor. The results provide evidence that antibody polyreactivity can result from local, rather than global, features of an antibody and that addition of <italic>N</italic>‐linked glycosylation can be an<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Antibody polyreactivity can be an obstacle to translating a candidate antibody into a clinical product. Standard tests such as antibody binding to cardiolipin, HEp‐2 cells, or nuclear antigens provide measures of polyreactivity, but its causes and the means to resolve are often unclear. Here we present a method for eliminating antibody polyreactivity through the computational design and genetic addition of <italic>N</italic>‐linked glycosylation near known sites of polyreactivity. We used the HIV‐1‐neutralizing antibody, VRC07, as a test case, since efforts to increase VRC07 potency at three spatially distinct sites resulted in enhanced polyreactivity. The addition of <italic>N</italic>‐linked glycans proximal to the polyreactivity‐enhancing mutations at each of the spatially distinct sites resulted in reduced antibody polyreactivity as measured by (i) anti‐cardiolipin ELISA, (ii) Luminex AtheNA Multi‐Lyte ANA binding, and (iii) HEp‐2 cell staining. The reduced polyreactivity trended with increased antibody concentration over time in mice, but not with improved overall protein stability as measured by differential scanning calorimetry. Moreover, glycan proximity to the site of polyreactivity appeared to be a critical factor. The results provide evidence that antibody polyreactivity can result from local, rather than global, features of an antibody and that addition of <italic>N</italic>‐linked glycosylation can be an effective approach to reducing antibody polyreactivity.</p> </abstract> … (more)
- Is Part Of:
- Protein science. Volume 24:Number 6(2015:Jun.)
- Journal:
- Protein science
- Issue:
- Volume 24:Number 6(2015:Jun.)
- Issue Display:
- Volume 24, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 24
- Issue:
- 6
- Issue Sort Value:
- 2015-0024-0006-0000
- Page Start:
- 1019
- Page End:
- 1030
- Publication Date:
- 2015-05-12
- Subjects:
- Proteins -- Periodicals
572.6 - Journal URLs:
- http://www.proteinscience.org/ ↗
http://www3.interscience.wiley.com/journal/121502357/ ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1002/pro.2682 ↗
- Languages:
- English
- ISSNs:
- 0961-8368
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.105500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4291.xml