A strategy for enrichment of claudins based on their affinity to Clostridium perfringens enterotoxin.

ABSTRACT:

Background

Claudins, a family of protein localized in tight junctions, are essential for the control of paracellular permeation in epithelia and endothelia. The interaction of several claudins with Clostridium perfringens enterotoxin (CPE) has been exploited for an affinity-based enrichment of CPE-binding claudins from lysates of normal rat cholangiocytes.

Results

Immunoblotting and mass spectrometry (MS) experiments demonstrate strong enrichment of the CPE-binding claudins -3, -4 and -7, indicating specific association with glutathione-S-transferase (GST)-CPE(116-319) fusion protein. In parallel, the co-elution of (non-CPE-binding) claudin-1 and claudin-5 was observed. The complete set of co-enriched proteins was identified by MS after electrophoretic separation. Relative m

SUBMITTER: Lohrberg D 

PROVIDER: S-EPMC2713237 | biostudies-literature | 2009 Jun

REPOSITORIES: biostudies-literature