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Wang, G.-F.

Publications and source records attributed to Wang, G.-F..

2 recordsLinked to original sources

Maize TIR-only Proteins ZmTIR1 and ZmTIR2, but not ZmTIR3 Confer Auto-active Hypersensitive Response Likely by Forming Condensation

Nucleotide binding, leucine-rich-repeat (NLR) proteins are the major intracellular receptors for defending against pathogen infection. The recognition between NLRs and pathogen secreted effectors often triggers a localized programmed cell death termed hypersensitive response (HR). Despite significant progresses have been achieved in understanding canonical NLRs with the N-terminal Toll/interleukin-1 receptor (TIR) domains, the molecular mechanisms underlying TIR-only proteins in plant immune responses remain unclear. In this study, we identified six TIR-containing proteins in maize, including three TIR-only proteins. Functional analysis showed that ZmTIR1 and ZmTIR2, but not ZmTIR3, confer autoactive HR when transiently expressed in N. benthamiana. The autoactivity conferred by ZmTIR1 and ZmTIR2 depends on EDS1-PAD4-RNL module and their putative NADase activities. Interestingly, ZmTIR1 and ZmTIR2 predominantly localize in the punctate dots and likely form condensation, while ZmTIR3 mainly localizes in the cytoplasm and the nucleus. Two specific amino acids in the BB-loop region were identified to be required for ZmTIR1- and ZmTIR2-mediated condensation formation and auto-HR. Furthermore, ZmTIR and ZmTIR2 are induced by Cochliobolus heterostrophus, the causal agent of southern leaf blight (SLB) in maize, and knock-down the expression of ZmTIR1 or ZmTIR2 decreased the resistance to SLB in maize. Our study reveals a novel mechanism of monocot TIR-only proteins in maize immune responses.

plant biology↗

Exploring Abeta42 Monomer Diffusive Dynamics on Fibril Surfaces through Molecular Simulations

This study provides critical insights into the role of surface-mediated secondary processes in Alzheimers disease, particularly regarding the aggregation of Abeta42 peptides. Employing coarse-grained molecular dynamics simulations, we focus on elucidating the molecular intricacies of these secondary processes beyond primary nucleation. Central to our investigation is the analysis of a freely diffusing Abeta42 monomer on pre-formed fibril structures. We conduct detailed calculations of the monomers diffusion coefficient on fibril surfaces (as a one-dimensional case), along with various monomer orientations. Our findings reveal a strong and consistent correlation between the monomers diffusion coefficient and its orientation on the surface. Further analysis differentiates the effects of parallel and perpendicular alignments with respect to the fibril axis. Additionally, we explore how different fibril surfaces influencemonomer dynamics by comparing the C-terminal and N-terminal surfaces. We find that the monomer exhibits lower diffusion coefficients on the N-terminal surface. Differences in surface roughness (SR), quantified using root-mean-square distances, significantly affect monomer dynamics, thereby influencing the secondary aggregation process. Importanly, this study underscores that fibril twisting acts as a regulatory niche, selectively influencing these orientations and their diffusion properties necessary for facilitating fibril growth within biologically relevant time scales. This discovery opens new avenues for targeted therapeutic strategies aimed at manipulating fibril dynamics to mitigate the progression of Alzheimers disease. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=168 SRC="FIGDIR/small/582685v3_ufig1.gif" ALT="Figure 1"> View larger version (33K): org.highwire.dtl.DTLVardef@f94f0eorg.highwire.dtl.DTLVardef@1b5362corg.highwire.dtl.DTLVardef@1f7aea9org.highwire.dtl.DTLVardef@1ec109f_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗