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The quantum efficiency of fluorescence was measured for simple derivatives of indole and phenol and for tryptophyl and tyrosyl residues in peptides and proteins. Fluorescence of these compounds decreased as the electronegativity of substituents increased. In proteins, one strongly electronegative structure is the peptide bond.

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Microcrystals of l-Asn-d-Trp-l-Phe-NH (NdWFamide), a tripeptide derived from Aplysia kurodai that exhibits invertebrate cardiac activity, were evaluated by vibrational circular dichroism (VCD). The chirality of the tryptophan residue at the second position in NdWFamide was associated with the conformation and biological characteristics. The VCD spectrum of NdWFamide was a mirror image of its enantiomer; however, it was significantly different from that of its diastereomer, NWFamide, which is its precursor.

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Proton transfer through membrane-bound ion channels is mediated by both water and polar residues of proteins, but the detailed molecular mechanism is challenging to determine. The tetrameric influenza A and B virus M2 proteins form canonical proton channels that use an HxxxW motif for proton selectivity and gating. The BM2 channel also contains a second histidine (His), H27, equidistant from the gating tryptophan, which leads to a symmetric HxxxWxxxH motif.

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T-cell priming occurs when a naïve T cell recognizes cognate peptide-MHC complexes on an activated antigen-presenting cell. The circumstances of this initial priming have ramifications on the fate of the newly primed T cell. Newly primed CD8 T cells can embark onto different trajectories, with some becoming short-lived effector cells and others adopting a tissue resident or memory cell fate.

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Anti-inflammatory Effects of PMX205 in Mouse Macrophage Periodontitis Model.

Iran J Immunol

June 2018

Department of Periodontics, School of Stomatology, Jilin University, Changchun, Jilin, China.

Background: C5a receptor antagonist PMX205 is a synthetic hexapeptide capable of blocking C5a-C5a receptor (C5aR) axis by simulating C5a active C-terminal amino acid residues. This hexapeptide presents good anti-inflammatory effects in a series of inflammation models. The anti-inflammatory effect of PMX205 on periodontitis is yet to be fully fathomed.

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