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Helicobacter pylorican cause various gastric conditions including stomach cancer in an acidic environment. Although early H. pyloriinfections can be treated by antibiotics, prolonged antibiotic administrations may lead to the development of antimicrobial resistance, compromising the effectiveness of the treatments. Antimicrobial peptides (AMPs) have been reported to possess unique advantages against antimicrobial-resistant bacteria due to their rapid physical membrane disruptions and anti-inflammation/immunoregulation properties. Herein, we have developed an AMP hydrogel, which can be orally administered for the treatment of H. pyloriinfection. The hydrogel has potent antimicrobial activity against H. pylori, achieving bacterial eradication within minutes of action. Compared with the AMP solution, the hydrogel formulation significantly reduced the cytotoxicity and enhanced proteolytic stability. In vivoexperiments suggested that the hydrogel formed at pH 4 had superior therapeutic effects to those at pH 7 and 10 hydrogels, attributed to its rapid release and bactericidal action within the acidic stomach environment. Compared to conventional antibiotic treatments, the AMP hydrogel had the advantages of fast bacterial killing in the gastric juice and obviated proton pump inhibitors during the treatment. Although both the AMP hydrogel and antibiotics suppressed the expression of pro-inflammatory cytokines, the former uniquely promoted inflammation resolution. These results indicate that the AMP hydrogels with effectiveness and biosafety may be potential candidates for the clinical treatment of H. pyloriinfections.

Nonionic surfactants used in agri-spraying processes may cause varying degrees of corneal irritation when they come in direct contact with farmers’ eyes, and the exact irritations are thought to be determined by how surfactants interact with corneal cell membranes. However, how nonionic surfactants interact with cell membranes at the molecular and nano levels remains largely unexplored. In this study, the interactions between nonionic surfactants (alkyl ethoxylate, C12Em) and lipid membranes were examined by membrane permeability measurement, quartz crystal microbalance with dissipation, dual polarization interferometry, confocal laser scanning microscopy, and neutron reflection, aiming to reveal complementary structural features at the molecular and nano levels. Apart from the extremely hydrophobic surfactant C12E2, all nonionic surfactants studied could penetrate the model cell membrane composed of a phosphocholine lipid bilayer. Nonionic surfactants with intermediate amphiphilicity (C12E6) rapidly fused into the lipid membrane and stimulated the formation of pores across the lipid bilayer, consistent with the cytoplasm leakage and fast cell necrosis observed from the cytotoxicity study of corneal cells. In comparison, while hydrophobic and hydrophilic surfactants [those with long and short ethoxylates (C12E4,12,23)] could cause mild structural alteration to the outer lipid layer of the membrane, these structural changes were insufficient to elicit large cytoplasmic leakage rapidly and instead cell death occurred over longer periods of time due to changes in the membrane permeability. These results reveal the strong link of surfactant–lipid membrane interactions to surfactant cytotoxicity and the association with amphiphilicity of nonionic surfactants.

Interfacial adsorption of monoclonal antibodies (mAbs) can cause structural deformation and induce undesired aggregation and precipitation. Nonionic surfactants are often added to reduce interfacial adsorption of mAbs which may occur during manufacturing, storage, and/or administration. As mAbs are commonly manufactured into ready-to-use syringes coated with silicone oil to improve lubrication, it is important to understand how an mAb, nonionic surfactant, and silicone oil interact at the oil/water interface. In this work, we have coated a polydimethylsiloxane (PDMS) nanofilm onto an optically flat silicon substrate to facilitate the measurements of adsorption of a model mAb, COE-3, and a commercial nonionic surfactant, polysorbate 80 (PS-80), at the siliconized PDMS/water interface using spectroscopic ellipsometry and neutron reflection. Compared to the uncoated SiO2surface (mimicking glass), COE-3 adsorption to the PDMS surface was substantially reduced, and the adsorbed layer was characterized by the dense but thin inner layer of 16 Å and an outer diffuse layer of 20 Å, indicating structural deformation. When PS-80 was exposed to the pre-adsorbed COE-3 surface, it removed 60 wt % of COE-3 and formed a co-adsorbed layer with a similar total thickness of 36 Å. When PS-80 was injected first or as a mixture with COE-3, it completely prevented COE-3 adsorption. These findings reveal the hydrophobic nature of the PDMS surface and confirm the inhibitory role of the nonionic surfactant in preventing COE-3 adsorption at the PDMS/water interface.

Aim: To analyze the worldwide epidemiology of lip and oral cavity cancer attributable to smoking. Methods: The worldwide epidemiology of lip and oral cavity cancer attributable to smoking and its spatial distribution differences were analyzed using the age-standardized mortality rate, age-standardized disability-adjusted life years (DALYs) rate, and estimated annual percent change (EAPC) according to information from the Global Burden of Disease Study 2019. Results: The number of deaths and DALYs associated with lip and oral cavity cancer attributable to smoking globally showed upward trends from 1990 to 2019, but the age-standardized mortality and DALYs rates decreased. The age-standardized mortality rate gradually increased with age. The age-standardized mortality and DALYs rates were markedly higher in low-middle social development index (SDI) regions than in other regions. The age-standardized mortality and DALYs rates showed slight increasing trends (EAPC = 0.16 and 0.07, respectively) in middle-SDI regions and the greatest decrease (EAPC = –1.60 and –1.74, respectively) in high-SDI regions. The three regions with the highest age-standardized mortality and DALYs rates were South Asia (1.59; 39.68), Eastern Europe (1.33; 40.59), and Central Europe (1.30; 37.67), but the largest increases were observed in East Asia (EAPC = 2.32, EAPC = 2.30), the Northern Mariana Islands (EAPC = 3.79, EAPC = 3.67), and Cabo Verde (EAPC = 2.84; DALY, EAPC = 3.38). Conclusion: The overall disease burden attributable to smoking is decreasing, but the number of deaths and DALYs are still increasing. Moreover, there are regional and national differences, and high-risk regions and countries should implement targeted interventions to reduce the burden.

Grain boundaries (GBs) have been shown to initiate metal halide perovskite degradation under light, moisture, and/or heat stresses due to the existence of various defects, making them extremely vulnerable in perovskite solar cells (PSCs). Although various post-treatments have been proven to be effective in repairing GBs, preventing the degradation from perovskite GBs remains an extremely difficult challenge. We report here a generic pre-annealing treatment for reconstructing sequentially deposited perovskite crystallites and GBs. With this strategy, robust GBs are created upon defect suppression with preferred oriented large perovskite grains. As a result, the resultant n-i-p-structured PSCs deliver an impressive power conversion efficiency of nearly 25% and an extremely high fill factor of 85.5%. The unencapsulated cells maintain 81% of their initial efficiencies after 1,000 h of continuous operation at maximum power point at about 55°C in an inert atmosphere, showing greatly improved light stability.

Peptide self-assembly is a hierarchical process during which secondary structures formed in the initial stages play a critical role in determining the subsequent assembling processes and final structural ordering. Unusual secondary structures hold promise as a source to develop novel supramolecular architectures with unique properties. In this work, we report the design of a new peptide self-assembly strategy based on unusual α-sheet secondary structures. In light of the strong propensity of leucine toward forming helical conformations and its high hydrophobicity, we design two short amphiphilic peptides Ac-LDLLDLK-NH2and Ac-DLLDLLDK-NH2with alternating l- and d-form amino acids. Microscopic imaging, neutron scattering, and spectroscopic measurements indicate that the two heterochiral peptides form highly ordered wide nanotubes and helical ribbons with monolayer thickness, in sharp contrast to twisted nanofibrils formed by the homochiral peptide Ac-LLLLK-NH2. Molecular dynamics simulations from monomers to trimers reveal that the two heteropeptides fold into α-sheets instead of β-sheets, which readily pack into tubular architectures in oligomer simulations. Simulated circular dichroism spectra based on α-sheet oligomers validate the proposed α-sheet secondary structures. These results form an important basis for the rational design of higher-order peptide assemblies with novel properties based on unusual α-sheet secondary structures.

Wide-bandgap (WBG) Methylammonium (MA)-free based perovskite solar cells (PSCs) have attracted widespread research interests due to their broad applicability in multijunction tandem. Nevertheless, the efficiency of WBG PSCs is restricted by unfulfilled potential in fill factor and large deficits in open-circuit voltage. The imbalanced carrier mobility not only plays a critical role in bulk non-radiative recombination loss but also hinders efficient charge collection for mixed I/Br WBG perovskites. Herein, we introduced additive named 2,8-Diiododibenzothiophene to overcome above issues. Inverted devices with enhanced photostability and a record fill factor of 85.7 % are demonstrated. Moreover, combining the semitransparent WBG PSCs with 1.25 eV-bandgap perovskite bottom cells, we realized 4-terminal tandem devices and a champion PCE of 28 % is achieved. The multifunctional additive strategy demonstrated here, will open new avenues for improving WBG PSCs’ performance.

Metallic lead (Pb0) impurities in metal-halide perovskites have attracted tremendous research concerns owing to their detrimental effects on perovskite solar cells (PSCs). However, the origins and influences of the Pb0behind this issue have yet to be well understood. Herein, we show that Pb0is hardly formed in the growth of halide perovskites but is easily postformed in the perovskite films with excess PbI2. It is found that Pb0impurities are decomposition byproducts of residual PbI2in perovskites under light or X-ray irradiation. Therefore, PSCs obtained using photodegraded PbI2films show large efficiency and stability losses. By contrast, the perovskite devices without detectable Pb0impurities have a much better efficiency and stability. This work reveals the origins and influences of Pb0in halide perovskites and provides a strategy for avoiding the formation of detrimental Pb0byproducts, which would drive further enhancements in device performance of halide perovskite solar cells, detectors, etc.

Mg-doped SnO2inserted between FTO and CdS manipulates the morphology of CdS/Sb2S3heterojunction and suppresses carrier recombination. The resultant solar cells deliver a remarkable champion efficiency of 6.31%.

The Qinling Mountain Range (QMR) spans a large region in China and is an important area of hominin activities. Many Paleolithic sites are found in Bahe, South Luohe, and Hanjiang river valleys in the northern, eastern, and southern part of the range, respectively. The Danjiang River valley acts as a channel connecting these valleys and stretches from the north to the south of the QMR. The previous dating of the Paleolithic sites in the Danjiang valley mainly relied on geomorphologic comparison, stratigraphic correlation, fossil characteristics, and Paleolithic artifacts, indicating a lack of absolute data. In this study, we conducted a detailed geochronological investigation of the entire valley, and selected an ideal site—the Miaokou profile. Based on the identification of the loess-paleosol sequences, optically stimulated luminescence, and magnetostratigraphy, the Paleolithic artifacts of the Miaokou site located within the S5 and S6 layers of the profile belong to ∼0.6–0.7 Ma. This suggests that the Paleolithic site is an old site in the Danjiang River valley, and this period also witnessed a rapid increase in the number of hominin sites during the Middle Pleistocene. Combining our results with previous reports across the QMR, we propose that the Danjiang River valley might have been a corridor for hominin migration, and is worthy of further investigation.

Antimicrobial peptides are promising alternatives to traditional antibiotics. A group of self-assembling lipopeptides was formed by attaching an acyl chain to the N-terminus of α-helix-forming peptides with the sequence Cx-G(IIKK)yI-NH2(CxGy, x= 4–12 and y= 2). CxGyself-assemble into nanofibers above their critical aggregation concentrations (CACs). With increasing x, the CACs decrease and the hydrophobic interactions increase, promoting secondary structure transitions within the nanofibers. Antimicrobial activity, determined by the minimum inhibition concentration (MIC), also decreases with increasing x, but the MICs are significantly smaller than the CACs, suggesting effective bacterial membrane-disrupting power. Unlike conventional antibiotics, both C8G2and C12G2can kill Staphylococcus aureusand Escherichia coliafter only minutes of exposure under the concentrations studied. C12G2nanofibers have considerably faster killing dynamics and lower cytotoxicity than their nonaggregated monomers. Antimicrobial activity of peptide aggregates has, to date, been underexploited, and it is found to be a very promising mechanism for peptide design. Detailed evidence for the molecular mechanisms involved is provided, based on superresolution fluorescence microscopy, solid-state nuclear magnetic resonance, atomic force microscopy, neutron scattering/reflectivity, circular dichroism, and Brewster angle microscopy.

Wide-band gap (WBG) mixed-halide perovskites have drawn much attention because of their excellent optoelectronic properties and the potential to be deployed in tandem solar cells. Nevertheless, the bromine incorporation inevitably leads to photoinduced phase segregation in WBG mixed-halide perovskites. Herein, potassium is used to effectively suppress photoinduced phase segregation, which is visualized with confocal photoluminescence microscopy imaging. Strikingly, the potassium passivation not only inhibits the formation of the narrow-band gap subphase but also enhances the crystallinity of the WBG mixed-halide perovskite. In addition, the potassium-passivated WBG perovskite exhibits lower defect density, longer charge carrier lifetime, and better photostability. As a result, the optimized KI (2 mol %)-passivated WBG perovskite solar cells (PSCs) deliver a champion power conversion efficiency of 18.3% with negligible hysteresis. They maintain 98% of their initial efficiency after 400 h under 100 mW·cm–2white light illumination in nitrogen.

Molecular dynamics (MD) simulations, stochastic optical reconstruction microscopy (STORM), and neutron reflection (NR) were combined to explore how antimicrobial peptides (AMPs) can be designed to promote the formation of nanoaggregates in bacterial membranes and impose effective bactericidal actions. Changes in the hydrophobicity of the designed AMPs were found to have a strong influence on their bactericidal potency and cytotoxicity. G(IIKK)3I-NH2(G3) achieved low minimum inhibition concentrations (MICs) and effective dynamic kills against both antibiotic-resistant and -susceptible bacteria. However, a G3derivative with weaker hydrophobicity, KI(KKII)2I-NH2(KI), exhibited considerably lower membrane-lytic activity. In contrast, the more hydrophobic G(ILKK)3L-NH2(GL) peptide achieved MICs similar to those observed for G3but with worsened hemolysis. Both the model membranes studied by Brewster angle microscopy, zeta potential measurements, and NR and the real bacterial membranes examined with direct STORM contained membrane-inserted peptide aggregates upon AMP exposure. These structural features were well supported by MD simulations. By revealing how AMPs self-assemble in microbial membranes, this work provides important insights into AMP mechanistic actions and allows further fine-tuning of antimicrobial potency and cytotoxicity.

Antimony selenosulfide (Sb2(S,Se)3) has been emerging as a promising light absorber owing to its tunable bandgap (1.1–1.7 eV), high absorption coefficient (>105cm−1), and excellent phase and environmental stability. Lithium salt‐doped 2,2′,7,7′‐tetrakis(N,N‐di‐p‐methoxy‐phenylamine)‐9,9′‐spirobifluorene (spiro‐OMeTAD) has been generally used as the hole transport layer (HTL) in these high‐efficiency antimony selenosulfide solar cells so far. However, the lithium‐ion reactions and migration in this HTL may cause serious challenges for the stability of these solar cells. Herein, stable and low‐cost tin monosulfide (SnS) nanoparticles surface‐modified nickel oxide (NiOx) as an inorganic hole transport layer to fabricate highly efficient and stable all‐inorganic solar cells is developed. It is found that NiOxfilms not only demonstrate a higher conductivity but also form better energy band alignment after SnS surface treatment. Consequently, the power conversion efficiency of the full inorganic Sb2(S,Se)3solar cells increases from 4.85% to 6.41%. Most importantly, the devices also demonstrate much improved thermal, moisture, and long‐term stabilities as compared to the solar cells with spiro‐OMeTAD hole transport layer. The nickel oxide (NiOx) film with tin monosulfide treatment shows higher conductivity and hole carrier mobility. Furthermore, the NiOxfilms can form a better energy band alignment and the power conversion efficiency of optimized all‐inorganic antimony selenosulfide solar cells increases from 4.85% to 6.41%. In addition, the all‐inorganic cells manifest excellent stability as compared with the organic devices.

A versatile material-antimony potassium tartrate is added to wide-bandgap perovskite cells for the first time.Inverted wide-bandgap perovskite solar cells with a structure of ITO/MeO-2PACz/perovskite/C60/ALD-SnO2/Cu yield a champion power conversion efficiency of 20.35%.A perovskite/perovskite four-terminal tandem solar cell with efficiency of 26.3% is achieved.

The physical stability of a monoclonal antibody (mAb) solution for injection in a prefilled syringe may in part depend on its behavior at the silicone oil/water interface. Here, the adsorption of a mAb (termed COE-3) and its fragment antigen-binding (Fab) and crystallizable (Fc) at the oil/water interface was measured using neutron reflection. A 1.4 ± 0.1 μm hexadecane oil film was formed on a sapphire block by a spin–freeze–thaw process, retaining its integrity upon contact with the protein solutions. Measurements revealed that adsorbed COE-3 and its Fab and Fc fragments retained their globular structure, forming layers that did not penetrate substantially into the oil phase. COE-3 and Fc were found to adsorb flat-on to the interface, with denser 45 and 42 Å inner layers, respectively, in contact with the oil and a more diffuse 17–21 Å outer layer caused by fragments adsorbing in a tilted manner. In contrast, Fab fragments formed a uniform 60 Å monolayer. Monolayers were formed under all conditions studied (10–200 ppm, using three isotopic contrasts), although changes in packing density across the COE-3 and Fc layers were observed. COE-3 had a higher affinity to the interface than either of its constituent fragments, while Fab had a lower interfacial affinity consistent with its higher net surface charge. This study extends the application of high-resolution neutron reflection measurements to the study of protein adsorption at the oil/water interface using an experimental setup mimicking the protein drug product in a siliconized prefilled syringe.

Antimicrobial peptides (AMPs) can target bacterial membranes and kill bacteria through membrane structural damage and cytoplasmic leakage. A group of surfactant-like cationic AMPs was developed from substitutions to selective amino acids in the general formula of G(IIKK)3I-NH2, (called G3, a de novo AMP), to explore the correlation between AMP hydrophobicity and bioactivity. A threshold surface pressure over 12 mN/m was required to cause measurable antimicrobial activity and this corresponded to a critical AMP concentration. Greater surface activity exhibited stronger antimicrobial activity but had the drawback of worsening hemolytic activity. Small unilamellar vesicles (SUVs) with specific lipid compositions were used to model bacterial and host mammalian cell membranes by mimicking the main structural determinants of the charge and composition. Leakage from the SUVs of encapsulated carboxyfluorescein measured by fluorescence spectroscopy indicated a negative correlation between hydrophobicity and model membrane selectivity, consistent with measurements of the zeta potential that demonstrated the extent of AMP binding onto model SUV lipid bilayers. Experiments with model lipid membranes thus explained the trend of minimum inhibitory concentrations and selectivity measured from real cell systems and demonstrated the dominant influence of hydrophobicity. This work provides useful guidance for the improvement of the potency of AMPs via structural design, whilst taking due consideration of cytotoxicity.

Mixed thermoreversible gels were successfully fabricated by the addition of a thermosensitive polymer, poly(N-isopropylacrylamide) (PNIPAM), to fibrillar nanostructures self-assembled from a short peptide I3K. When the temperature was increased above the lower critical solution temperature of the PNIPAM, the molecules collapsed to form condensed globular particles, which acted as cross-links to connect different peptide nanofibrils and freeze their movements, resulting in the formation of a hydrogel. Since these processes were physically driven, such hydrogels could be reversibly switched between the sol and gel states as a function of temperature. As a model peptide, I3K was formulated with PNIPAM to produce a thermoreversible sol–gel system with a transition temperature of ∼33 °C, which is just below the body temperature. The antibacterial peptide of G(IIKK)3I-NH2could be conveniently encapsulated in the hydrogel by the addition of the solution at lower temperatures in the sol phase and then increasing the temperature to be above 33 °C for gelation. The hydrogel gave a sustained and controlled linear release of G(IIKK)3I-NH2over time. Using the peptide nanofibrils as three-dimensional scaffolds, such thermoresponsive hydrogels mimic the extracellular matrix and could potentially be used as injectable hydrogels for minimally invasive drug delivery or tissue engineering.

During the formulation of therapeutic monoclonal antibodies (mAbs), nonionic surfactants are commonly added to attenuate structural rearrangement caused by adsorption/desorption at interfaces during processing, shipping, and storage. We examined the adsorption of a mAb (COE-3) at the SiO2/water interface in the presence of pentaethylene glycol monododecyl ether (C12E5), polysorbate 80 (PS80-20EO), and a polysorbate 80 analogue with seven ethoxylates (PS80-7EO). Spectroscopic ellipsometry was used to follow COE-3 dynamic adsorption, and neutron reflection was used to determine interfacial structure and composition. Neither PS80-20EO nor C12E5had a notable affinity for COE-3 or the interface under the conditions studied and thus did not prevent COE-3 adsorption. In contrast, PS80-7EO did coadsorb but did not influence the dynamic process or the equilibrated amount of absorbed COE-3. Near equilibration, COE-3 underwent structural rearrangement and PS80-7EO started to bind the COE-3 interfacial layer and subsequently formed a well-defined surfactant bilayer via self-assembly. The resultant interfacial layer comprised an inner mAb layer of about 70 Å thickness and an outer surfactant layer of a further 70 Å, with distinct transitional regions across the mAb–surfactant and surfactant–bulk water boundaries. Once formed, such interfacial layers were very robust and worked to prevent further mAb adsorption, desorption, and structural rearrangement. Such robust interfacial layers could be anticipated to exist for formulated mAbs stored in type II glass vials; further research is required to understand the behavior of these layers for siliconized glass syringes.

Mixed lead and tin (Pb-Sn) halide perovskites promise high-performance solar cells because of their narrow bandgaps and other outstanding essential properties. However, there is still a big gap between the performance of the practical devices and theoretical limitations. Here we investigate key factors for realizing high-performance narrow-bandgap Pb-Sn perovskite solar cells (PSCs) via numerical simulations. We first study the effects of extrinsic factors on device performance, which predicts that a p-i-n structure along with appropriate charge transport layers is superior to an n-i-p structure, benefiting from a better energy band alignment. We further investigate key intrinsic factors and demonstrate that surface defect density, body defect density, and film thickness of perovskite absorbers play a pivotal role in determining device performance. The simulation results imply that narrow-bandgap Pb-Sn PSCs with fully-powered optimization should be able to realize a power conversion efficiency of 28.56%. Motivated by the simulations, we also successfully fabricate efficient narrow-bandgap Pb-Sn single-junction and 4-terminal all-perovskite tandem PSCs, which deliver high efficiencies of 21.01% and 26.01% measured under reverse voltage scans, respectively. This work points the way toward the improvement of narrow-bandgap Pb-Sn PSCs in the future.

Cationic biocides have been widely used as active ingredients in personal care and healthcare products for infection control and wound treatment for a long time, but there are concerns over their cytotoxicity and antimicrobial resistance. Designed lipopeptides are potential candidates for alleviating these issues because of their mildness to mammalian host cells and their high efficacy against pathogenic microbial membranes. In this study, antimicrobial and cytotoxic properties of a de novo designed lipopeptide, CH3(CH2)12CO-Lys-Lys-Gly-Gly-Ile-Ile-NH2(C14KKGGII), were assessed against that of two traditional cationic biocides CnTAB (n= 12 and 14), with different critical aggregation concentrations (CACs). C14KKGGII was shown to be more potent against both bacteria and fungi but milder to fibroblast host cells than the two biocides. Biophysical measurements mimicking the main features of microbial and host cell membranes were obtained for both lipid monolayer models using neutron reflection and small unilamellar vesicles (SUVs) using fluorescein leakage and zeta potential changes. The results revealed selective binding to anionic lipid membranes from the lipopeptide and in-membrane nanostructuring that is distinctly different from the co-assembly of the conventional CnTAB. Furthermore, CnTAB binding to the model membranes showed low selectivity, and its high cytotoxicity could be attributed to both membrane lysis and chemical toxicity. This work demonstrates the advantages of the lipopeptides and their potential for further development toward clinical application.

Gram-negative bacteria are covered by both an inner cytoplasmic membrane (IM) and an outer membrane (OM). Antimicrobial peptides (AMPs) must first permeate through the OM and cell wall before attacking the IM to cause cytoplasmic leakage and kill the bacteria. The bacterial OM is an asymmetric bilayer with the outer leaflet primarily composed of lipopolysaccharides (LPSs) and the inner leaflet composed of phospholipids (PLs). Two cationic α-helical AMPs were designed to target Gram-negative bacteria, a full peptide G(IIKK)3I-NH2(G3), and a hydrophobic lipopeptide C8-G(IIKK)2I-NH2(C8G2, with C8denoting the octanoyl chain). LPS dominates OM functions as the first line of defense against antibiotics, thereby reducing drug susceptibility. This work explores how the two AMPs interact with LPS through several carefully chosen OM models that facilitated measurements from solid-state nuclear magnetic resonance (ss-NMR), small-angle neutron scattering (SANS), and neutron reflectivity (NR). The results revealed that G3molecules bound preferably to the LPS head region and functioned as bridge molecules to reassemble the dislocated lipids into bilayer stacks. In contrast, C8G2lipopeptides could quickly penetrate into the central region of the OM to cause direct removal of some membrane lipids. Different structural disruptions implicated different antimicrobial efficacies from these AMPs. The demonstration of the structural features underlying different susceptibilities of the OM to AMPs offers a useful route for the future development of strain-specific AMPs against antimicrobial-resistant pathogens.