Journal:Acta Cryst D:S2059798324008210
From Proteopedia
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By refining our data collection methods, we successfully determined the MicroED structure of TLR2TIR-induced MyD88TIR microcrystals, achieving superior resolution (2.85 Å) and completeness (89%) compared to the previously studied MALTIR-induced MyD88TIR microcrystals. Notably, both types of assemblies showed distinct conformational differences in regions critical for signaling, such as the BB loop and CD loop, when compared to their monomeric structures. These findings suggest that TLR2TIR and MALTIR interact with MyD88 in a similar manner, promoting the unidirectional nucleation of MyD88TIR assemblies during signaling. This highlights the unique role of TLR2TIR in modulating MyD88 assembly and signaling, offering new insights into the specificity and dynamics of TLR-mediated immune responses. | By refining our data collection methods, we successfully determined the MicroED structure of TLR2TIR-induced MyD88TIR microcrystals, achieving superior resolution (2.85 Å) and completeness (89%) compared to the previously studied MALTIR-induced MyD88TIR microcrystals. Notably, both types of assemblies showed distinct conformational differences in regions critical for signaling, such as the BB loop and CD loop, when compared to their monomeric structures. These findings suggest that TLR2TIR and MALTIR interact with MyD88 in a similar manner, promoting the unidirectional nucleation of MyD88TIR assemblies during signaling. This highlights the unique role of TLR2TIR in modulating MyD88 assembly and signaling, offering new insights into the specificity and dynamics of TLR-mediated immune responses. | ||
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+ | Fig_7a | ||
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<b>References</b><br> | <b>References</b><br> | ||
<references/> | <references/> | ||
</StructureSection> | </StructureSection> | ||
__NOEDITSECTION__ | __NOEDITSECTION__ |
Revision as of 17:59, 13 October 2024
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