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9GFH

BCR Fab from the subset 1 chronic lymphocytic leukaemia case P1173

Summary for 9GFH
Entry DOI10.2210/pdb9gfh/pdb
DescriptorBCR P1173 light chain, BCR P1173 heavy chain, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total)
Functional Keywordsb-cell receptor, fab fragment, chronic lymphocytic leukaemia, immune system
Biological sourceHomo sapiens
More
Total number of polymer chains8
Total formula weight193632.22
Authors
Cocomazzi, P.G.,Degano, M. (deposition date: 2024-08-09, release date: 2025-08-20, Last modification date: 2026-01-14)
Primary citationCocomazzi, P.G.,Iatrou, A.,Minici, C.,Gounari, M.,Linder, A.T.,Akpinaroglu, C.,Patrone, M.,Broggini, L.,Frenquelli, M.,Sarrigeorgiou, I.,Lymberi, P.,Petrakis, G.,Koletsa, T.,Scarfo, L.,Agathangelidis, A.,Jumaa, H.,Maity, P.C.,Ghia, P.,Stamatopoulos, K.,Degano, M.
Defective cell-autonomous signalling and antigenic polyreactivity of B-cell receptors from chronic lymphocytic leukaemia stereotyped subset 1.
Nat Commun, 2025
Cited by
PubMed Abstract: A shared feature of B-cell receptors (BCRs) expressed on neoplastic B cells from patients with chronic lymphocytic leukaemia (CLL) concerns their continual activation of intracellular signalling without requiring external antigens. This autonomous signalling mechanism has previously been demonstrated to arise from BCR-BCR homotypic interactions in three distinct stereotyped CLL subsets (2, 4 and 169). CLL subset 1 is the second largest stereotyped subset, epitomizing unmutated CLL and known for a particularly aggressive clinical course. Here we show that, despite their significant sequence similarity, BCRs originating from three different subset 1 CLL cases exhibit variations in their combining site structures and associated physicochemical properties. Subset 1 BCRs are characterized by a common reactivity pattern towards various autoantigens, though they maintain distinct receptor-specific characteristics. Analysis of crystal structures of the respective BCR Fab fragments reveals lack of conservation in intermolecular crystal contacts, paralleled by no self-association in solution and incapacity to induce intracellular signalling when expressed in a model B-cell line. These findings suggest that cell-autonomous signalling may not be universally present across all CLL, implying the existence of other mechanisms in sustaining leukemic cell proliferation and CLL progression mediated by BCR signalling.
PubMed: 41469389
DOI: 10.1038/s41467-025-68040-5
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.72 Å)
Structure validation

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