Elasticity, an often-overseen parameter in the development of nanoscale drug delivery systems

• Agnes-Valencia Weiss and
• Marc Schneider

Beilstein J. Nanotechnol. 2023, 14, 1149–1156, doi:10.3762/bjnano.14.95

• provides different possibilities of measuring forces at the nanoscale. This can be the acquisition of single force–distance curves on a specific spot after locating the particle in an imaging mode or the creation of whole maps using quantitative imaging modes [20][21][22]. An example is shown for lysozyme

Bioselectivity of silk protein-based materials and their bio-inspired applications

• Hendrik Bargel,
• Vanessa T. Trossmann,
• Christoph Sommer and
• Thomas Scheibel

Beilstein J. Nanotechnol. 2022, 13, 902–921, doi:10.3762/bjnano.13.81

• with membrane perturbation and dissipation of the transmembrane potential, which results in bacterial cell lysis and death [92]. In humans, over 120 HDPs have been identified, and typical examples include lysozyme, defensins, histatins, lactoferricin, kinocidins, ribonuclease, dermcidin, and

Gelatin nanoparticles with tunable mechanical properties: effect of crosslinking time and loading

• Agnes-Valencia Weiss,
• Daniel Schorr,
• Julia K. Metz,
• Metin Yildirim,
• Saeed Ahmad Khan and
• Marc Schneider

Beilstein J. Nanotechnol. 2022, 13, 778–787, doi:10.3762/bjnano.13.68

• contrast to this, lysozyme as a crosslinkable macromolecule did not influence the mechanical properties. A good in vitro cell compatibility was found investigating blank GNPs and FITC-dextran-loaded GNPs in viability assays with the cancer cell line A549 and the human primary cell-derived hAELVi cell line

• for 0.5 h imaged under liquid conditions by AFM are shown in Figure 1. Incorporating lysozyme as a protein drug up to an initial loading of 3 mg per 20 mg gelatin resulted in particles with comparable size (242.67 ± 11.32 nm), size distribution (0.132 ± 0.04), and a negative zeta potential at neutral

• macromolecule to the matrix should, following our explanation, not show an effect on the elasticity of the particles as no “defects” in the network will be introduced. In line with this explanation, lysozyme-loaded GNPs exhibited a particle elasticity not significantly different from unloaded GNPs. Regarding

Design and selection of peptides to block the SARS-CoV-2 receptor binding domain by molecular docking

• Kendra Ramirez-Acosta,
• Ivan A. Rosales-Fuerte,
• J. Eduardo Perez-Sanchez,
• Alfredo Nuñez-Rivera,
• Josue Juarez and
• Ruben D. Cadena-Nava

Beilstein J. Nanotechnol. 2022, 13, 699–711, doi:10.3762/bjnano.13.62

• through ADV, 69 of the 104 APD peptides bound stronger to the RBD active region than the ACE2 peptide (Table 1 and Table S2, Supporting Information File 1). Three peptides based on lysozyme were also designed for screening to compare with the APD peptides given the antimicrobial role of lysozyme as part

• affinity values are higher for those APD peptides bound to the RBD with a high number of hydrogen bonds and hydrophobic interactions [47]. Table 1 shows that twelve APD and three lysozyme peptides surpass the binding energy calculated for the ACE2 peptide to the RBD (−4.6 kcal/mol), indicating that these

• of the protein–ligand complex, novel peptides were designed considering the most common amino acid residues from the 13 APD and lysozyme peptides that bind to the RBD active region through hydrogen bonds [35]. This task is easy to develop in comparison to the typical procedures used in standard

A comprehensive review on electrospun nanohybrid membranes for wastewater treatment

• Senuri Kumarage,
• Imalka Munaweera and
• Nilwala Kottegoda

Beilstein J. Nanotechnol. 2022, 13, 137–159, doi:10.3762/bjnano.13.10

• membrane incorporating halloysite nanotubes (HNTs) filled with lysozyme (50 wt % of lysozyme) into Polyamide 11 (PA11) as a bio-based pad for extending the shelf life of chicken slices and has found that the filled nanohybrid membrane resulted in a reduction of bacterial growth compared to electrospun PA11

Comprehensive review on ultrasound-responsive theranostic nanomaterials: mechanisms, structures and medical applications

• Sepand Tehrani Fateh,
• Lida Moradi,
• Elmira Kohan,
• Michael R. Hamblin and
• Amin Shiralizadeh Dezfuli

Beilstein J. Nanotechnol. 2021, 12, 808–862, doi:10.3762/bjnano.12.64

• %, respectively [207]. Liao et al. fabricated epidermal growth factor-coated lysozyme MBs responsive to US waves, which showed good antimicrobial activity, promoting neovascularization and significantly reducing the time needed for wound healing

Fabrication of nano/microstructures for SERS substrates using an electrochemical method

• Jingran Zhang,
• Tianqi Jia,
• Xiaoping Li,
• Junjie Yang,
• Zhengkai Li,
• Guangfeng Shi,
• Xinming Zhang and
• Zuobin Wang

Beilstein J. Nanotechnol. 2020, 11, 1568–1576, doi:10.3762/bjnano.11.139

• . Additionally, a 10−6 mol·L−1 solution of lysozyme was successfully detected using the Mg–Au nanopore substrates. Our low-cost method is reproducible, homogeneous, and suitable for the fabrication of SERS substrates. Keywords: electrochemical machining; gold (Au); lysozyme detection; magnesium (Mg); micro

• nanostructures were fabricated by controlling the treatment time and R6G molecules were chosen to be adsorbed onto the substrate. Finally, the Raman intensities of low concentrations of lysozyme were determined using arrayed structures as the SERS substrates. Using this approach allows for the accurate

• could be detected. Thus, the electrochemical method can be used to create flexible Au-coated substrates of highly reproducible structure with long-term stability. SERS measurement of lysozyme on the nanopore substrates The enzyme lysozyme can rupture the cell walls of certain pathogens following

Electrokinetic characterization of synthetic protein nanoparticles

• Daniel F. Quevedo,
• Cody J. Lentz,
• Adriana Coll de Peña,
• Yazmin Hernandez,
• Nahal Habibi,
• Rikako Miki,
• Joerg Lahann and
• Blanca H. Lapizco-Encinas

Beilstein J. Nanotechnol. 2020, 11, 1556–1567, doi:10.3762/bjnano.11.138

• composed of BSA and lysozyme. Two types of particles were synthesized: particles that were homogenous blends of proteins and anisotropic particles. A total of eight distinct types of SPNPs were electrokinetically characterized. The results illustrate that particle composition strongly influences the

• composed of different proteins EK microfluidics could potentially be used to separate SPNPs of two different proteins based on size and ζp value. Thus, we next investigated the trapping voltage of SPNPs composed of two commonly used model proteins, BSA and lysozyme. The two proteins have significantly

• different isoelectric points, 11.35 for lysozyme and 5.4 for BSA. This difference in isoelectric point implies that the two particles would behave differently in an EK device. SPNPs were synthesized using two main proteins: lysozyme (SPNP-Lys-488) or BSA (SPNP-BSA-488). The particles were fully

Luminescent gold nanoclusters for bioimaging applications

• Nonappa

Beilstein J. Nanotechnol. 2020, 11, 533–546, doi:10.3762/bjnano.11.42

• importantly, the Au-BSA NCs are stable under ambient conditions and retain their PL even after drying (Figure 1G,H) allowing for long-term storage [64]. Several other proteins including lysozyme, human serum albumin (HSA) and insulin have been used to prepare inherently luminescent AuNCs [65][66][67][68][69

• citrate reduction of Au(III) salts resulting in core–shell (IO@Au) nanoparticles of 9.3 ± 2.6 nm. The core–shell particles underwent lysozyme-mediated aggregation (IO@Au-Lys). The aggregated structures were further treated with Au-BSA NCs (IO@Au-Lys-Au-BSA) to form a composite structure. The combination

• : glutathione; NAC: N-acetylcysteine; MTU: 5-methyl-2-thiouracil). D) Structures of biomolecular ligands (HSA: human serum albumin, PDB ID IE78; BSA: bovine serum albumin, PDB ID 3VO3, and Lys: lysozyme, PDB ID 3WUN). E) Schematic representation showing Au-BSA NC synthesis. F) Absorbance and fluorescence

Advanced hybrid nanomaterials

• Andreas Taubert,
• Fabrice Leroux,
• Pierre Rabu and
• Verónica de Zea Bermudez

Beilstein J. Nanotechnol. 2019, 10, 2563–2567, doi:10.3762/bjnano.10.247

• for sensing or corrosion protection. To understand composite formation of a complex hybrid assembly, high quality characterization is paramount. An example is small angle X-ray scattering (SAXS), which was used in the work “Mechanism of silica–lysozyme composite formation unraveled by in situ fast

• SAXS” to identify and characterize subtle interparticle interactions [24]. This study shows that fast in situ synchrotron SAXS provides an understanding of lysozyme deformation molecules during aggregation. All these contributions indicate a marked interest of current research in hybrid materials for

Targeted therapeutic effect against the breast cancer cell line MCF-7 with a CuFe₂O₄/silica/cisplatin nanocomposite formulation

• B. Rabindran Jermy,
• Vijaya Ravinayagam,
• Widyan A. Alamoudi,
• Dana Almohazey,
• Hatim Dafalla,
• Lina Hussain Allehaibi,
• Abdulhadi Baykal,
• Muhammet S. Toprak and
• Thirunavukkarasu Somanathan

Beilstein J. Nanotechnol. 2019, 10, 2217–2228, doi:10.3762/bjnano.10.214

• -shell support thickness of about 50 nm was reported with a high ferrite loading capacity of about 30–50 wt % with particle diameters between 9 and 17 nm (at the external carbon layer). Such a magnetic nanoformulation was found to be useful for enzyme lysozyme immobilization. The magnetic properties of

Materials nanoarchitectonics at two-dimensional liquid interfaces

• Katsuhiko Ariga,
• Michio Matsumoto,
• Taizo Mori and
• Lok Kumar Shrestha

Beilstein J. Nanotechnol. 2019, 10, 1559–1587, doi:10.3762/bjnano.10.153

Mechanism of silica–lysozyme composite formation unravelled by in situ fast SAXS

• Tomasz M. Stawski,
• Daniela B. van den Heuvel,
• Rogier Besselink,
• Dominique J. Tobler and
• Liane G. Benning

Beilstein J. Nanotechnol. 2019, 10, 182–197, doi:10.3762/bjnano.10.17

• inorganic nanoparticles (NPs) and proteins in aqueous media is of paramount interest for colloid chemistry. In particular, the interactions between silica (SiO2) NPs and lysozyme (LZM) have attracted attention, because LZM is well-known to adsorb strongly to silica NPs, while at the same time preserving its

• originating from the presence of LZM. We developed a scattering model and applied it to analyse this structure function, which allowed us to extract structural information on the deformation of lysozyme molecules during aggregation, as well as to derive the mechanisms of composite formation. Keywords

• : composite; lysozyme; scattering; silica; small-angle X-ray scattering (SAXS); Introduction A mechanistic understanding of aggregation in aqueous media leading to the formation of composites of inorganic nanoparticles and proteins is of paramount interest for colloid chemistry, Earth sciences, or the design

Protein-coated pH-responsive gold nanoparticles: Microwave-assisted synthesis and surface charge-dependent anticancer activity

• Dickson Joseph,
• Nisha Tyagi,
• Christian Geckeler and
• Kurt E.Geckeler

Beilstein J. Nanotechnol. 2014, 5, 1452–1462, doi:10.3762/bjnano.5.158

• ]. Biomolecules have been reported to interact with gold salts and reduce them into metallic gold, acting both as a reductant and stabilizer [12][17][18][19][20][21]. Proteins, such as bovine serum albumin, silk fibroin protein, chicken egg white lysozyme, α-amylase, green fluorescent protein and apoferritin have

• and non-irradiated. Based on Figure S3 (Supporting Information File 1), we observed that non-globular monomer proteins, such as lysozyme (LYS) and histone (HIS), did not undergo any change in their UV absorbance, whereas globular monomer proteins, such as ovalbumin (OVA) and BSA, showed an increase in

• histone (HIS), chicken egg white lysozyme (LYS), ovalbumin (OVA), bovine serum albumin (BSA), bovine hemoglobin (BHG), bovine gamma globulin (BGG), glucose oxidase (Aspergillus niger) (GOX), and trypsin (porcine pancreas, TRY), used for the experiments were obtained from Sigma (USA) as a lyophilized

Detection of interaction between biomineralising proteins and calcium carbonate microcrystals

• Hanna Rademaker and
• Malte Launspach

Beilstein J. Nanotechnol. 2011, 2, 222–227, doi:10.3762/bjnano.2.26

• aragonite microcrystals. Generally, this could be expected due to the greater specific surface area of the aragonite microcrystals used compared to the calcite microcrystals. Nonetheless a lysozyme control experiment shows that unspecific binding cannot be the only reason for the larger amount of protein in

• lane A (here lane A from Figure 3). This control experiment shows the influence of the greater specific surface area of aragonite on the SDS-PAGE results, assuming unspecific binding of lysozyme to both, aragonite and calcite. A difference in intensities in lanes A and C from Figure 3 due only to

• of chitin associated proteins) and their relative intensity in lane A (aragonite associated proteins) shows an increased relative concentration of the one indicated by the orange arrow in lane A. To estimate the detection limit for proteins in this experiment, different quantities of lysozyme were