Algal chloroplast produced camelid VHH antitoxins are capable of neutralizing botulinum neurotoxin. Issue 1 (17th September 2014)
- Record Type:
- Journal Article
- Title:
- Algal chloroplast produced camelid VHH antitoxins are capable of neutralizing botulinum neurotoxin. Issue 1 (17th September 2014)
- Main Title:
- Algal chloroplast produced camelid VHH antitoxins are capable of neutralizing botulinum neurotoxin
- Authors:
- Barrera, Daniel J.
Rosenberg, Julian N.
Chiu, Joanna G.
Chang, Yung‐Nien
Debatis, Michelle
Ngoi, Soo‐Mun
Chang, John T.
Shoemaker, Charles B.
Oyler, George A.
Mayfield, Stephen P. - Abstract:
- <abstract abstract-type="main" id="pbi12244-abs-0001"> <title>Summary</title> <p>We have produced three antitoxins consisting of the variable domains of camelid heavy chain‐only antibodies (V<sub>H</sub>H) by expressing the genes in the chloroplast of green algae. These antitoxins accumulate as soluble proteins capable of binding and neutralizing botulinum neurotoxin. Furthermore, they accumulate at up to 5% total soluble protein, sufficient expression to easily produce these antitoxins at scale from algae. The genes for the three different antitoxins were transformed into <italic>Chlamydomonas reinhardtii</italic> chloroplasts and their products purified from algae lysates and assayed for <italic>in vitro</italic> biological activity using toxin protection assays. The produced antibody domains bind to botulinum neurotoxin serotype A (BoNT/A) with similar affinities as camelid antibodies produced in <italic>Escherichia coli</italic>, and they are similarly able to protect primary rat neurons from intoxication by BoNT/A. Furthermore, the camelid antibodies were produced in algae without the use of solubilization tags commonly employed in <italic>E. coli</italic>. These camelid antibody domains are potent antigen‐binding proteins and the heterodimer fusion protein containing two V<sub>H</sub>H domains was capable of neutralizing BoNT/A at near equimolar concentrations with the toxin. Intact antibody domains were detected in the gastrointestinal (GI) tract of mice treated<abstract abstract-type="main" id="pbi12244-abs-0001"> <title>Summary</title> <p>We have produced three antitoxins consisting of the variable domains of camelid heavy chain‐only antibodies (V<sub>H</sub>H) by expressing the genes in the chloroplast of green algae. These antitoxins accumulate as soluble proteins capable of binding and neutralizing botulinum neurotoxin. Furthermore, they accumulate at up to 5% total soluble protein, sufficient expression to easily produce these antitoxins at scale from algae. The genes for the three different antitoxins were transformed into <italic>Chlamydomonas reinhardtii</italic> chloroplasts and their products purified from algae lysates and assayed for <italic>in vitro</italic> biological activity using toxin protection assays. The produced antibody domains bind to botulinum neurotoxin serotype A (BoNT/A) with similar affinities as camelid antibodies produced in <italic>Escherichia coli</italic>, and they are similarly able to protect primary rat neurons from intoxication by BoNT/A. Furthermore, the camelid antibodies were produced in algae without the use of solubilization tags commonly employed in <italic>E. coli</italic>. These camelid antibody domains are potent antigen‐binding proteins and the heterodimer fusion protein containing two V<sub>H</sub>H domains was capable of neutralizing BoNT/A at near equimolar concentrations with the toxin. Intact antibody domains were detected in the gastrointestinal (GI) tract of mice treated orally with antitoxin‐producing microalgae. These findings support the use of orally delivered antitoxins produced in green algae as a novel treatment for botulism.</p> </abstract> … (more)
- Is Part Of:
- Plant biotechnology journal. Volume 13:Issue 1(2015:Jan.)
- Journal:
- Plant biotechnology journal
- Issue:
- Volume 13:Issue 1(2015:Jan.)
- Issue Display:
- Volume 13, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 13
- Issue:
- 1
- Issue Sort Value:
- 2015-0013-0001-0000
- Page Start:
- 117
- Page End:
- 124
- Publication Date:
- 2014-09-17
- Subjects:
- Plant biotechnology -- Periodicals
Plant genetic engineering -- Periodicals
630.272 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1467-7652 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=pbi ↗
http://www.blackwellpublishing.com/journal.asp?ref=1467-7644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/pbi.12244 ↗
- Languages:
- English
- ISSNs:
- 1467-7644
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6513.780000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3572.xml