| Literature DB >> 17431183 |
Alexander J Bankovich1, Stefan Raunser, Z Sean Juo, Thomas Walz, Mark M Davis, K Christopher Garcia.
Abstract
The pre-B cell receptor (pre-BCR) serves as a checkpoint in B cell development. In the 2.7 angstrom structure of a human pre-BCR Fab-like fragment, consisting of an antibody heavy chain (HC) paired with the surrogate light chain, the "unique regions" of VpreB and lambda5 replace the complementarity-determining region 3 (CDR3) loop of an antibody light chain and appear to "probe" the HC CDR3, potentially influencing the selection of the antibody repertoire. Biochemical analysis indicates that the pre-BCR is impaired in its ability to recognize antigen, which, together with electron microscopic visualization of a pre-BCR dimer, suggests ligand-independent oligomerization as the likely signaling mechanism.Entities:
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Year: 2007 PMID: 17431183 DOI: 10.1126/science.1139412
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728