Antimicrobial peptides (AMPs), as a key component of the immune defense systems of organisms, are a promising solution to the serious threat of drug-resistant bacteria to public health. As one of the most representative and extensively studied AMPs, melittin has exceptional broad-spectrum activities against microorganisms, including both Gram-positive and Gram-negative bacteria. Unfortunately, the action mechanism of melittin with bacterial membranes, especially the underlying physics of peptide-induced membrane poration behaviors, is still poorly understood, which hampers efforts to develop melittin-based drugs or agents for clinical applications. In this mini-review, we focus on recent advances with respect to the membrane insertion behavior of melittin mostly from a computational aspect. Membrane insertion is a prerequisite and key step for forming transmembrane pores and bacterial killing by melittin, whose occurrence is based on overcoming a high free-energy barrier during the transition of melittin molecules from a membrane surface-binding state to a transmembrane-inserting state. Here, intriguing simulation results on such transition are highlighted from both kinetic and thermodynamic aspects. The conformational changes and inter-peptide cooperation of melittin molecules, as well as melittin-induced disturbances to membrane structure, such as deformation and lipid extraction, are regarded as key factors influencing the insertion of peptides into membranes. The associated intermediate states in peptide conformations, lipid arrangements, membrane structure, and mechanical properties during this process are specifically discussed. Finally, potential strategies for enhancing the poration ability and improving the antimicrobial performance of AMPs are included as well.

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This study aimed to develop an effective method to fabricate the amphiphobic polyvinylidene fluoride (PVDF) composite membranes for membrane distillation (MD) with excellent tolerance to various organic foulants. A facial surface modification method was explored to obtain amphiphobic membranes with mechanical and thermal robustness by dynamically forming perfluorooctyl trichlorosilane (PFTS) and coating SiO 2 nanoparticles onto the membrane surface. A variety of techniques such as environmental scanning electron microscopy (ESEM), Fourier transform infrared spectrometry (FTIR), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), liquid entry pressure (LEP) measurement and contact angle goniometry were applied to examine the effects of surface modification on surface chemistry, morphology and wettability of the derived 

Antimicrobial peptides (AMPs) promise a fundamental solution to the devastating threat of drug‐resistant bacteria. However, drawbacks of AMPs (e.g., poor cell membrane penetration efficiency) seriously block their clinical use. In this work, rational design of a hybrid complex of melittin (as a representative AMP) and graphene or graphene oxide (Gra or GO) nanosheets for enhanced antibacterial ability is achieved, via combining in‐silico prediction and in‐tube test. In comparison to pristine melittin, the specifically designed AMP‐Gra (/GO) complex exhibits remarkable efficiency in transmembrane perforation with an over tenfold decrease in the threshold working concentration of peptide; moreover, it has an up to 20‐fold enhancement in antibacterial activity against both Gram‐negative and Gram‐positive bacteria. Such improvement is ascribed to the synergetic insertion of nanosheets and melittin due to similarity in antibacterial mechanism between them and is further regulated by the structural factors of the complex, including the intersheet spacing and surface functionalization of the Gra/GO sheets, etc. These results provide practical guidelines to engineer AMPs with nanotechnology for improved antimicrobial performances, especially based on targeted functionalization of the Gra/GO nanosheets.

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