Skip Navigation



PEDS Advance Access published online on September 19, 2006

Protein Engineering Design and Selection, doi:10.1093/protein/gzl036
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
19/11/497    most recent
gzl036v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Barkhordarian, H.
Right arrow Articles by Sierks, M. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Barkhordarian, H.
Right arrow Articles by Sierks, M. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Received May 8, 2006
Revised July 17, 2006
Accepted July 20, 2006

Article

Isolating recombinant antibodies against specific protein morphologies using atomic force microscopy and phage display technologies

Hedieh Barkhordarian 1, Sharareh Emadi 1, Philip Schulz 1, and Michael R. Sierks 1 *

1 Department of Chemical and Materials Engineering, Arizona State University, Tempe, AZ, USA

* To whom correspondence should be addressed.
Michael R. Sierks, E-mail: sierks{at}asu.edu


   Abstract

Isolation of antibodies to antigens that are either unstable, exist in multiple morphologies or have very limited availability can be prohibitively difficult. Here we describe a novel technique combining the capabilities of phage display antibody technology and atomic force microscopy (AFM) that is used to isolate antibody fragments that bind to a specific morphology of the target antigen, {alpha}-synuclein. AFM imaging allows us to both visualize the presence and morphology of the target antigen as well as to monitor the efficiency of each step in the bio-panning process. We demonstrate that phage displayed antibodies specific to the target antigen morphology can be isolated after only two rounds of selection. The target antigen, {alpha}-synuclein, has been correlated with the Parkinson's disease (PD). Accumulation of {alpha}-synuclein fibrillar aggregates into Lewy body inclusions is a hallmark feature of PD. While {alpha}-synuclein can form several different aggregate morphologies including oligomers, protofibrils and fibrils, the role of these morphologies in the progression of PD is not known. The successful selection of the recombinant antibody described here can have potential therapeutic value since the single-chain fragment variable (scFv) can be expressed intracellularly to control folding and toxicity of the specific protein aggregates.

Keywords: antibodies; atomic force microscopy; bio-panning; phage display; protein morphology.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
S. Emadi, S. Kasturirangan, M. S. Wang, P. Schulz, and M. R. Sierks
Detecting Morphologically Distinct Oligomeric Forms of {alpha}-Synuclein
J. Biol. Chem., April 24, 2009; 284(17): 11048 - 11058.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.