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Biology subjects

Zan, B.

Publications and source records attributed to Zan, B..

2 recordsLinked to original sources

Dynamic exchange of antimicrobial peptides stabilize persistent lipid pores

Antimicrobial peptides (AMPs) are a promising broad-spectrum complement to conventional antibiotics. But despite their relatively simple structures, the reported modes of action of AMPs are diverse, ranging from formation of stable ion-channel-like structures, or disruption of biochemical pathways, to comprehensive membrane solubilization. This apparent complexity of function is a significant hurdle in their future application and rational design. Here, we combine single-molecule tracking with optical single-channel recording in synthetic mimics of bacterial membranes to image the pores formed by AMPs in real time, mapping the diffusion of individual AMPs relative to sites of membrane permeablization. Using alamethicin, magainin-II and melittin as archetypes of three principal membrane-disrupting AMP classes, we observe AMP molecules freely diffusing on the membrane, but with an enhancement of local peptide surface density within a nanoscopic region surrounding each pore locus. We do not observe this enhancement for indolicidin, an AMP which is not believed to use pore formation as its main mode of toxicity. Corroborated by molecular dynamics simulations that replicate our experiments, these results suggest defects formed by membrane-active AMPs are persistent but dynamic structures, stabilised by individual peptides free to diffuse into and out of the pore. Whilst alamethicin, magainin-II and melittin are often placed in different mechanistic pore-forming groups, the broad similarities between observations in these different AMPs encourages a continuum view of pore-forming ability, rather than discrete categories of mechanism.

biophysics↗

Mn2+-Induced Structural Flexibility Enhances the Entire Catalytic Cycle and the Cleavage of Mismatches in Prokaryotic Argonaute Proteins

Prokaryotic Argonaute (pAgo) proteins, a class of DNA/RNA-guided programmable endonucleases, have been extensively utilized in nucleic acid biosensors. The specific binding and cleavage of nucleic acids by pAgo proteins, which are crucial processes for their applications, are dependent on the presence of Mn2+ bound in the pockets, as verified through X-ray crystallography. However, a comprehensive understanding of how dissociated Mn2+ in the solvent affects the catalytic cycle, and its underlying regulatory role in this structure-function relationship, remains underdetermined. By combining experimental and computational methods, this study reveals that unbound Mn2+ in solution enhances the flexibility of diverse pAgo proteins. This increase in flexibility through decreasing the number of hydrogen bonds, induced by Mn2+, leads to higher affinity for substrates, thus facilitating cleavage. More importantly, Mn2+-induced structural flexibility increases the mismatch tolerance between guide-target pairs by increasing the conformational states, thereby enhancing the cleavage of mismatches. Further simulations indicated that the enhanced flexibility in linkers triggers conformational changes in the PAZ domain for recognizing various lengths of nucleic acids. Additionally, Mn2+-induced dynamic alterations of the protein cause a conformational shift in the N domain and catalytic sites towards their functional form, resulting in a decreased energy penalty for target release and cleavage. These findings demonstrate that the dynamic conformations of pAgo proteins, resulting from the presence of the unbound Mn2+ in solution, significantly promote the catalytic cycle of endonucleases and the tolerance of cleavage to mismatches. This flexibility enhancement mechanism serves as a general strategy employed by Ago proteins from diverse prokaryotes to accomplish their catalytic functions and provide useful information for Ago-based precise molecular diagnostics.

biophysics↗