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6GR0

Petrobactin-binding engineered lipocalin in complex with gallium-petrobactin

Summary for 6GR0
Entry DOI10.2210/pdb6gr0/pdb
DescriptorNeutrophil gelatinase-associated lipocalin, 4-[4-[3-[[3,4-bis(oxidanyl)phenyl]carbonylamino]propylamino]butylamino]-2-[2-[4-[3-[[3,4-bis(oxidanyl)phenyl]carbonylamino]propylamino]butylamino]-2-oxidanylidene-ethyl]-2-oxidanyl-4-oxidanylidene-butanoic acid, GALLIUM (III) ION, ... (4 entities in total)
Functional Keywordsanticalin, beta-barrel, petrobactin, lcn2, lipocalin, ngal, protein engineering, transport protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains3
Total formula weight65202.57
Authors
Skerra, A.,Eichinger, A. (deposition date: 2018-06-08, release date: 2018-08-15, Last modification date: 2024-11-06)
Primary citationDauner, M.,Eichinger, A.,Lucking, G.,Scherer, S.,Skerra, A.
Reprogramming Human Siderocalin To Neutralize Petrobactin, the Essential Iron Scavenger of Anthrax Bacillus.
Angew. Chem. Int. Ed. Engl., 57:14619-14623, 2018
Cited by
PubMed Abstract: Bacillus anthracis owes its pronounced virulence-apart from specific toxins-to a twofold import mechanism for Fe ions. This pathogenic bacterium secretes the siderophores bacillibactin (BB) and petrobactin (PB), of which only BB is neutralized by human siderocalin, an abundant lipocalin in plasma. We describe its reshaping via combinatorial protein design to bind PB⋅Fe instead of BB⋅Fe , and with even higher affinity (K ≈20 pm). X-ray crystallographic analysis of the resulting "petrocalin" in complex with PB⋅Ga reveals a positively charged ligand pocket while the extended butterfly-like conformation of the bound PB provides a rationale for the missing recognition by the natural siderocalin. In microbiological studies, a combination of petrocalin and siderocalin effectively suppressed the growth of a BB /PB strain of Bacillus cereus under iron-limiting culture conditions. Thus, our reprogrammed lipocalin may offer novel treatment options for devastating infections caused by B. anthracis.
PubMed: 30063283
DOI: 10.1002/anie.201807442
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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