Recognition of pneumococcal peptidoglycan: an expanded, pivotal role for LPS binding protein (Q24317469)

defense response to Gram-positive bacterium

GOA release 2020-03-11

1 reference

Lipopolysaccharide binding protein

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Elaine I Tuomanen

8

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author name string

Joerg R Weber

1

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Dorette Freyer

2

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Christian Alexander

3

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Nicolas W J Schröder

4

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Anja Reiss

5

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Carsten Küster

6

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Dagmar Pfeil

7

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Ralf R Schumann

Crystal structure of human BPI and two bound phospholipids at 2.4 angstrom resolution

9

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language of work or name

English

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publication date

August 2003

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published in

Immunity

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volume

19

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issue

2

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page(s)

269-79

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cites work

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Production and release of peptidoglycan and wall teichoic acid polymers in pneumococci treated with beta-lactam antibiotics.

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A biological price of antibiotic resistance: major changes in the peptidoglycan structure of penicillin-resistant pneumococci

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LPS-binding protein protects mice from septic shock caused by LPS or gram-negative bacteria

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Digestion of Streptococcus pneumoniae cell walls with its major peptidoglycan hydrolase releases branched stem peptides carrying proinflammatory activity

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Drosophila Toll is activated by Gram-positive bacteria through a circulating peptidoglycan recognition protein

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Differential effects of p38- and extracellular signal-regulated kinase mitogen-activated protein kinase inhibitors on inducible nitric oxide synthase and tumor necrosis factor production in murine macrophages stimulated with Streptococcus pneumoniae

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Clinical outcome in pneumococcal meningitis correlates with CSF lipoteichoic acid concentrations

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Targeted deletion of the lipopolysaccharide (LPS)-binding protein gene leads to profound suppression of LPS responses ex vivo, whereas in vivo responses remain intact

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Pneumococcal licD2 gene is involved in phosphorylcholine metabolism.

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