Document Detail


Recognition imaging of chromatin and chromatin-remodeling complexes in the atomic force microscope.
MedLine Citation:
PMID:  18951183     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Atomic force microscopy (AFM) can directly visualize single molecules in solution, which makes it an extremely powerful technique for carrying out studies of biological complexes and the processes in which they are involved. A recent development, called Recognition Imaging, allows the identification of a specific type of protein in solution AFM images, a capability that greatly enhances the power of the AFM approach for studies of complex biological materials. In this technique, an antibody against the protein of interest is attached to an AFM tip. Scanning a sample with this tip generates a typical topographic image simultaneously and in exact spatial registration with a "recognition image." The latter identifies the locations of antibody-antigen binding events and thus the locations of the protein of interest in the image field. The recognition image can be electronically superimposed on the topographic image, providing a very accurate map of specific protein locations in the topographic image. This technique has been mainly used in in vitro studies of biological complexes and reconstituted chromatin, but has great potential for studying chromatin and protein complexes isolated from nuclei.
Authors:
Dennis Lohr; Hongda Wang; Ralph Bash; Stuart M Lindsay
Related Documents :
22847883 - Mesh in prolapse surgery: an imaging perspective.
23845053 - Aspects of sexual self-schema in premenopausal women with dyspareunia: associations wit...
15898543 - Radiometric framework for image mosaicking.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Methods in molecular biology (Clifton, N.J.)     Volume:  464     ISSN:  1940-6029     ISO Abbreviation:  Methods Mol. Biol.     Publication Date:  2009  
Date Detail:
Created Date:  2008-10-27     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9214969     Medline TA:  Methods Mol Biol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  123-38     Citation Subset:  IM    
Affiliation:
Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Mapping cis- and trans- chromatin interaction networks using chromosome conformation capture (3C).
Next Document:  Using cells encapsulated in agarose microbeads to analyse nuclear structure and functions.