2R0Z

PFA1 FAB complexed with GripI peptide fragment

Summary for 2R0Z

• Entry DOI: 10.2210/pdb2r0z/pdb
• Related: 2IPT 2IPU 2IQ9 2IQA 2R0W
• Descriptor: IgG2a Fab fragment light chain, IgG2a Fab fragment heavy chain, Fd portion, GripI peptide fragment, ... (5 entities in total)
• Functional Keywords: immunoglobulin; alzheimer disease; amyloid, immune system
• Biological source: Mus musculus (house mouse); More
• Total number of polymer chains: 3
• Total formula weight: 49167.84

Authors

Gardberg, A.S.,Dealwis, C. (deposition date: 2007-08-21, release date: 2007-10-16, Last modification date: 2017-10-25)

Primary citation

Gardberg, A.S.,Dice, L.T.,Ou, S.,Rich, R.L.,Helmbrecht, E.,Ko, J.,Wetzel, R.,Myszka, D.G.,Patterson, P.H.,Dealwis, C.
Molecular basis for passive immunotherapy of Alzheimer's disease
Proc.Natl.Acad.Sci.Usa, 104:15659-15664, 2007

PubMed Abstract: Amyloid aggregates of the amyloid-beta (Abeta) peptide are implicated in the pathology of Alzheimer's disease. Anti-Abeta monoclonal antibodies (mAbs) have been shown to reduce amyloid plaques in vitro and in animal studies. Consequently, passive immunization is being considered for treating Alzheimer's, and anti-Abeta mAbs are now in phase II trials. We report the isolation of two mAbs (PFA1 and PFA2) that recognize Abeta monomers, protofibrils, and fibrils and the structures of their antigen binding fragments (Fabs) in complex with the Abeta(1-8) peptide DAEFRHDS. The immunodominant EFRHD sequence forms salt bridges, hydrogen bonds, and hydrophobic contacts, including interactions with a striking WWDDD motif of the antigen binding fragments. We also show that a similar sequence (AKFRHD) derived from the human protein GRIP1 is able to cross-react with both PFA1 and PFA2 and, when cocrystallized with PFA1, binds in an identical conformation to Abeta(1-8). Because such cross-reactivity has implications for potential side effects of immunotherapy, our structures provide a template for designing derivative mAbs that target Abeta with improved specificity and higher affinity.

PubMed: 17895381
DOI: 10.1073/pnas.0705888104

Experimental method

X-RAY DIFFRACTION (2.096 Å)