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PDBsum entry 3wpd
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DNA binding protein/DNA
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PDB id
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3wpd
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DOI no:
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Nature
520:702-705
(2015)
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PubMed id:
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Structural basis of CpG and inhibitory DNA recognition by Toll-like receptor 9.
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U.Ohto,
T.Shibata,
H.Tanji,
H.Ishida,
E.Krayukhina,
S.Uchiyama,
K.Miyake,
T.Shimizu.
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ABSTRACT
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Innate immunity serves as the first line of defence against invading pathogens
such as bacteria and viruses. Toll-like receptors (TLRs) are examples of innate
immune receptors, which sense specific molecular patterns from pathogens and
activate immune responses. TLR9 recognizes bacterial and viral DNA containing
the cytosine-phosphate-guanine (CpG) dideoxynucleotide motif. The molecular
basis by which CpG-containing DNA (CpG-DNA) elicits immunostimulatory activity
via TLR9 remains to be elucidated. Here we show the crystal structures of three
forms of TLR9: unliganded, bound to agonistic CpG-DNA, and bound to inhibitory
DNA (iDNA). Agonistic-CpG-DNA-bound TLR9 formed a symmetric TLR9-CpG-DNA complex
with 2:2 stoichiometry, whereas iDNA-bound TLR9 was a monomer. CpG-DNA was
recognized by both protomers in the dimer, in particular by the amino-terminal
fragment (LRRNT-LRR10) from one protomer and the carboxy-terminal fragment
(LRR20-LRR22) from the other. The iDNA, which formed a stem-loop structure
suitable for binding by intramolecular base pairing, bound to the concave
surface from LRR2-LRR10. This structure serves as an important basis for
improving our understanding of the functional mechanisms of TLR9.
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');
}
}
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