Journal Article FZJ-2018-01104

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
Biophysical insights from a single chain camelid antibody directed against the disrupted in schizophrenia 1 protein

 ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;

2018
PLoS Lawrence, Kan.

PLoS one 13(1), e0191162 - () [10.1371/journal.pone.0191162]

This record in other databases:      

Please use a persistent id in citations:   doi:

Abstract: Accumulating evidence suggests an important role for the Disrupted-in-Schizophrenia 1 (DISC1) protein in neurodevelopment and chronic mental illness. In particular, the C-terminal 300 amino acids of DISC1 have been found to mediate important protein-protein interactions and to harbor functionally important phosphorylation sites and disease-associated polymorphisms. However, long disordered regions and oligomer-forming subdomains have so far impeded structural analysis. VHH domains derived from camelid heavy chain only antibodies are minimal antigen binding modules with appreciable solubility and stability, which makes them well suited for the stabilizing proteins prior to structural investigation. Here, we report on the generation of a VHH domain derived from an immunized Lama glama, displaying high affinity for the human DISC1 C region (aa 691–836), and its characterization by surface plasmon resonance, size exclusion chromatography and immunological techniques. The VHH-DISC1 (C region) complex was also used for structural investigation by small angle X-ray scattering analysis. In combination with molecular modeling, these data support predictions regarding the three-dimensional fold of this DISC1 segment as well as its steric arrangement in complex with our VHH antibody.

Classification:

Contributing Institute(s):
  1. Strukturbiochemie (ICS-6)
  2. Neutronenstreuung (Neutronenstreuung ; JCNS-1)
  3. Neutronenstreuung (ICS-1)
Research Program(s):
  1. 553 - Physical Basis of Diseases (POF3-553) (POF3-553)

Appears in the scientific report 2018
Database coverage:
Medline ; Creative Commons Attribution CC BY 4.0 ; DOAJ ; OpenAccess ; BIOSIS Previews ; DOAJ Seal ; Ebsco Academic Search ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; SCOPUS ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection ; Zoological Record
Click to display QR Code for this record

The record appears in these collections:
Dokumenttypen > Aufsätze > Zeitschriftenaufsätze
Institutssammlungen > JCNS > JCNS-1
Institutssammlungen > IBI > IBI-8
Institutssammlungen > IBI > IBI-7
Workflowsammlungen > Öffentliche Einträge
ICS > ICS-1
ICS > ICS-6
Publikationsdatenbank
Open Access

 Datensatz erzeugt am 2018-02-02, letzte Änderung am 2024-06-19


Dieses Dokument bewerten:

Rate this document:
1
2
3
 
(Bisher nicht rezensiert)