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7DM1

crystal structure of the M.tuberculosis phosphate ABC transport receptor PstS-1 in complex with Fab p4-36

Summary for 7DM1
Entry DOI10.2210/pdb7dm1/pdb
DescriptorPhosphate-binding protein PstS 1, light chain, heavy chain, ... (5 entities in total)
Functional Keywordsantibody, complex, transport protein, transprot protein-immune system complex, transprot protein/immune system
Biological sourceMycobacterium tuberculosis H37Rv
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Total number of polymer chains6
Total formula weight170969.35
Authors
Ma, B.,Freund, N.,Xiang, Y. (deposition date: 2020-12-01, release date: 2020-12-23, Last modification date: 2024-11-13)
Primary citationWatson, A.,Li, H.,Ma, B.,Weiss, R.,Bendayan, D.,Abramovitz, L.,Ben-Shalom, N.,Mor, M.,Pinko, E.,Bar Oz, M.,Wang, Z.,Du, F.,Lu, Y.,Rybniker, J.,Dahan, R.,Huang, H.,Barkan, D.,Xiang, Y.,Javid, B.,Freund, N.T.
Human antibodies targeting a Mycobacterium transporter protein mediate protection against tuberculosis.
Nat Commun, 12:602-602, 2021
Cited by
PubMed Abstract: Mycobacterium tuberculosis (Mtb) exposure drives antibody responses, but whether patients with active tuberculosis elicit protective antibodies, and against which antigens, is still unclear. Here we generate monoclonal antibodies from memory B cells of one patient to investigate the B cell responses during active infection. The antibodies, members of four distinct B cell clones, are directed against the Mtb phosphate transporter subunit PstS1. Antibodies p4-36 and p4-163 reduce Mycobacterium bovis-BCG and Mtb levels in an ex vivo human whole blood growth inhibition assay in an FcR-dependent manner; meanwhile, germline versions of p4-36 and p4-163 do not bind Mtb. Crystal structures of p4-36 and p4-170, complexed to PstS1, are determined at 2.1 Å and 2.4 Å resolution, respectively, to reveal two distinctive PstS1 epitopes. Lastly, a prophylactic p4-36 and p4-163 treatment in Mtb-infected Balb/c mice reduces bacterial lung burden by 50%. Our study shows that inhibitory anti-PstS1 B cell responses arise during active tuberculosis.
PubMed: 33504803
DOI: 10.1038/s41467-021-20930-0
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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