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Search for "proteins" in Full Text gives 395 result(s) in Beilstein Journal of Nanotechnology. Showing first 200.
Nanocarrier systems loaded with IR780, iron oxide nanoparticles and chlorambucil for cancer theragnostics
Beilstein J. Nanotechnol. 2024, 15, 180–189, doi:10.3762/bjnano.15.17
- DLS and PDI increased to approx. 280 nm and 0.24, respectively. The NPs were still well dispersed in cell culture media; however, the size increase suggested the adsorption of FBS proteins onto the NPs. The SEM results (Figure 1B) showed the actual size of the nanoparticles, which had a round shape of
- -life. When NPs are administered, they come into contact with blood cells and plasma proteins, which may cause adsorption or opsonization by serum proteins [35]. However, these proteins will have a reduced probability of interacting with our negatively charged nanoparticles, as most proteins are
Modification of graphene oxide and its effect on properties of natural rubber/graphene oxide nanocomposites
Beilstein J. Nanotechnol. 2024, 15, 168–179, doi:10.3762/bjnano.15.16
- were purchased from Sigma-Aldrich. Vinyltriethoxysilanes, tert-butyl hydroperoxide (TBHPO), and urea were purchased from Tokyo Chemical Industry, Japan. Removal of proteins from natural rubber According to the method reported in [24], deproteinization of HANR was carried out using urea as a denaturing
Assessing phytotoxicity and tolerance levels of ZnO nanoparticles on Raphanus sativus: implications for widespread adoptions
Beilstein J. Nanotechnol. 2024, 15, 115–125, doi:10.3762/bjnano.15.11
- at 1000 mg/L. Conversely, at a concentration of 2000 mg/L, ZnO NPs significantly reduced soluble proteins and increased IAA levels, indicating toxicity and physiological stress. Plants treated with a dose of 10,000 mg/L exhibited wilting and yellowing by day 18 and did not survive until day 45. A
Nanotechnological approaches in the treatment of schistosomiasis: an overview
Beilstein J. Nanotechnol. 2024, 15, 13–25, doi:10.3762/bjnano.15.2
- sublethal doses can cause alterations in parasite tegument [85]. Bee venom comprises various pharmacologically active components, including melittin (constituting more than 50% of total proteins) and a mixture of enzymes, cell-lytic peptides, proteases, and bioactive amines [86]. This mixture has
Fluorescent bioinspired albumin/polydopamine nanoparticles and their interactions with Escherichia coli cells
Beilstein J. Nanotechnol. 2023, 14, 1208–1224, doi:10.3762/bjnano.14.100
- ]. These properties can even be controlled by an external signal [17][18][19]. PDA NPs are formed upon oxidation in dopamine (DA) solutions with additives such as surfactants, polyelectrolytes, and proteins [14]. Eumelanin-like NPs with a diameter less than 20 nm have been obtained by this method. The
- structure of these albumin/PDA NPs has not been elucidated completely. It has been demonstrated that proteins are present in the NPs’ shell; they might also be present in the core (Figure 1d). Nevertheless, their potential both for fluorescent labelling of alive bacterial cells and as nanovector for
- between DA and BSA, which contains the KE diad and allows for the control of the NP formation [13]. During the synthesis, DA is added into the BSA solution, thus avoiding that the proteins come into contact with already formed PDA. Bergtold et al. proposed that the size control is exerted by the specific
Curcumin-loaded albumin submicron particles with potential as a cancer therapy: an in vitro study
Beilstein J. Nanotechnol. 2023, 14, 1127–1140, doi:10.3762/bjnano.14.93
- pharmacokinetic drawbacks such as poor water solubility resulting in low bioavailability, low absorption, rapid metabolism, and elimination [6][7]. The reported solubility of free CUR in distilled water at 25 °C is 1.34 µg/mL [8]. The conjugation of CUR with proteins has been confirmed to improve its aqueous
- Na2CO3 solutions in the presence of albumin [26][27]. This approach has been shown to have high effectiveness for entrapping various biopolymers (e.g., proteins and hemoglobin) into carbonate particles before dissolving with EDTA to obtain pure biopolymer submicron particles. The CCD technique is a
- albumin proteins [30]. CUR showed strong binding affinity towards HSA, likely at the tryptophan residue, which is present in the hydrophobic cavities of HSA [23][31]. The final CUR-HSA-MPs are obtained after dissolution of the MnCO3 template with EDTA. Characterization of CUR-HSA-MPs Dynamic light
Recognition mechanisms of hemoglobin particles by monocytes – CD163 may just be one
Beilstein J. Nanotechnol. 2023, 14, 1028–1040, doi:10.3762/bjnano.14.85
- scavenging and consecutive increase in peripheral vascular resistance. Whether binding between cell surface proteins and Hb/HBOC can occur, and how high the corresponding affinity is, probably depends on modifications made to Hb. Intramolecular crosslinking has an impact, depending on whether the binding
- × 1015 molecules/mL. The average Hpx serum concentration of 0.6 g/L corresponds to 4.5 × 1015 molecules/mL. Thus, the dose of 60 g HBOC 201 is sufficient to bind the available Hp and Hpx, allowing subsequent doses of HBOCs to remain in circulation until these proteins are replenished. In case of infusion
- since both proteins are specific for monocytes. CD163 was tested because of its direct affinity to Hb. Also, we tested the effect of blocking CD204 (scavenger receptor A/SR-A). SR-A is a membrane protein occurring in the monocyte/macrophage lineage. Playing an important role in host defense, it exhibits
Antibody-conjugated nanoparticles for target-specific drug delivery of chemotherapeutics
Beilstein J. Nanotechnol. 2023, 14, 912–926, doi:10.3762/bjnano.14.75
- active targeting via the functionalization of ligands, such as antibodies or proteins, that interact with receptors overexpressed at the target site [5][6]. However, the movement of NPs is hampered by biological barriers such as endothelial, cellular, skin, and mucosal barriers, which obstruct their
- targeting capabilities [7]. Researchers focused their interest on understanding the obstructions that impede targeted drug delivery, and several advances have been made to develop NPs with enhanced ability to cross these barriers. Bio-pharmacological drugs, which include recombinant proteins, monoclonal
- NPs specifically bind to the cell surface proteins and deliver the drug cargo to tumor sites via passive or active targeting. As a result, the therapeutic ratio is improved. At the same time, the systemic toxicity is reduced and the therapeutic efficacy is increased [13]. Antibody-conjugated NPs
Biomimetics on the micro- and nanoscale – The 25th anniversary of the lotus effect
Beilstein J. Nanotechnol. 2023, 14, 850–856, doi:10.3762/bjnano.14.69
- biological processes and surface interactions involved in the bioselective adhesion of mammalian cells. The second topic of the review was on repellence of microbes on protein-based material surfaces, highlighting the importance of materials made of recombinant spider silk proteins. Biomaterials that
Nanostructured lipid carriers containing benznidazole: physicochemical, biopharmaceutical and cellular in vitro studies
Beilstein J. Nanotechnol. 2023, 14, 804–818, doi:10.3762/bjnano.14.66
- intrinsic toxicity of our nanoscale vehicle on T. cruzi may be linked to a modification of glycosylphosphatidylinositols (GPIs). Glycosylphosphatidylinositols are the main anchor complexes used by protozoans to bind to cell surface proteins. It covalently attaches to the C terminus of a protein connecting
Silver nanoparticles loaded on lactose/alginate: in situ synthesis, catalytic degradation, and pH-dependent antibacterial activity
Beilstein J. Nanotechnol. 2023, 14, 781–792, doi:10.3762/bjnano.14.64
- antibacterial properties can serve as a source of silver ions. Another mechanism involves the electrostatic attraction between negatively charged microbial cells and positively charged AgNPs [25]. Because of their affinity to sulfur proteins and through electrostatic attraction, silver ions can bind to both
Metal-organic framework-based nanomaterials as opto-electrochemical sensors for the detection of antibiotics and hormones: A review
Beilstein J. Nanotechnol. 2023, 14, 631–673, doi:10.3762/bjnano.14.52
- , proteins, aptamers, and immunoglobulins) to realise an analyte-specific reaction. Because of their modification with biomolecules, some electrochemical biosensors have shown higher specificity and selectivity than unmodified electrochemical sensors; nevertheless, they have shorter lifetimes and poorer
Suspension feeding in Copepoda (Crustacea) – a numerical model of setae acting in concert
Beilstein J. Nanotechnol. 2023, 14, 603–615, doi:10.3762/bjnano.14.50
- -resolution CLSM imaging or atomic force microscopy. As it was visualized by CLSM [55][56][57], the basal parts of some short and long setae appear to be relatively soft and seem to contain resilin or other proteins. This should influence the mobility of the rotating setae. To account for this in the
Nanoarchitectonics to entrap living cells in silica-based systems: encapsulations with yolk–shell and sepiolite nanomaterials
Beilstein J. Nanotechnol. 2023, 14, 522–534, doi:10.3762/bjnano.14.43
- bionanocomposites that display biomimetic and bioinspired characteristics, derived from their biological components (e.g., polysaccharides, proteins, nucleic acids, enzymes and viruses, etc.) and the inorganic network (e.g., silica and silicates, clay minerals and phosphates) [5][6][7][8]. More complex biohybrid
Plasmonic nanotechnology for photothermal applications – an evaluation
Beilstein J. Nanotechnol. 2023, 14, 380–419, doi:10.3762/bjnano.14.33
New trends in nanobiotechnology
Beilstein J. Nanotechnol. 2023, 14, 377–379, doi:10.3762/bjnano.14.32
- the interaction between peptides with physiological proteins. Through the study, the selection and rapid design of peptides based on peptide binding sites, hydrogen bond number, and binding affinity were obtained. It was also concluded the potential role of these peptides in the prevention of
Quercetin- and caffeic acid-functionalized chitosan-capped colloidal silver nanoparticles: one-pot synthesis, characterization, and anticancer and antibacterial activities
Beilstein J. Nanotechnol. 2023, 14, 362–376, doi:10.3762/bjnano.14.31
- medium [74]. Since NPs are exposed to various forces that affect their stability and size in such environments (containing electrolytes, proteins and lipids), they may tend to collapse and aggregate. Although no aggregation and turbidity were observed during the preparation stage with the naked eye and
The steep road to nonviral nanomedicines: Frequent challenges and culprits in designing nanoparticles for gene therapy
Beilstein J. Nanotechnol. 2023, 14, 351–361, doi:10.3762/bjnano.14.30
- are assessed with the use of fluorescent-labeling carriers and the expression of fluorescent proteins (e.g., enhanced green fluorescent protein). Both of which are typically assessed by widefield fluorescent microscopy/confocal microscopy (referred to as “imaging”) and/or flow cytometry (Table 1
- of proteins after transfection. Because organelles (e.g., endosomes) are not uniformly distributed throughout the cell, these 2D imaging methods are rarely accurate for quantification of either uptake or transfection. Nevertheless, they still have been the methods of choice during the last five years
- particular type of NP can be measured using pharmacological inhibitors or genetic approaches that knockdown/knockout or transiently block the expression of key proteins involved in endocytosis [30]. Then, changes in NP uptake can be quantified and attributed to the significance of that pathway. Unfortunately
Polymer nanoparticles from low-energy nanoemulsions for biomedical applications
Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29
- , proteins, vaccines, and nucleotides [2]. In spite of biodegradability and biocompatibility, some studies have also demonstrated a certain concentration-dependent toxicologic profile including a mild inflammatory response after treatment with PLGA nanoparticles [49]. Some authors have suggested that the
- 5) with viabilities higher than 70% for HeLa cells are promising candidates for gene therapy (e.g., gene vaccines). Protein binding on PLGA nanoparticles prepared from nanoemulsions has also been studied [62]. After incubation with human serum, afamin was one of the specific proteins bound to PLGA
Overview of mechanism and consequences of endothelial leakiness caused by metal and polymeric nanoparticles
Beilstein J. Nanotechnol. 2023, 14, 329–338, doi:10.3762/bjnano.14.28
- determining vascular permeability are the intercellular junctions, which condition paracellular transport across the endothelium. There may be tight junctions between endothelial cells, mainly formed by occludin and claudin proteins. This type of connection is most characteristic of the central nervous system
- activation of mechanisms controlling the phosphorylation of proteins of intercellular junctions, which in turn opens the cell–cell junctions and creates gaps between the cells [13][17]. The use of appropriate vascular permeability stimulants can therefore be an effective solution in the treatment of diseases
- for the interaction with adherens junction proteins (e.g., VE-cadherin). The width of the endothelial gaps was ca. 22.5 nm [28]. Researchers observed that the interaction of the endothelium with NPs widens the existing gaps or induces new ones in the monolayer of vascular endothelial cells, thus
Bismuth-based nanostructured photocatalysts for the remediation of antibiotics and organic dyes
Beilstein J. Nanotechnol. 2023, 14, 291–321, doi:10.3762/bjnano.14.26
- the environment in low concentrations (micrograms per litre to nanograms per litre), are persistent and bioactive, potentially posing a threat to the food chain. Macrolides, fluoroquinolones, and tetracycline also have an impact on the synthesis of mitochondrial proteins and chloroplasts in plants [48
Biocatalytic synthesis and ordered self-assembly of silica nanoparticles via a silica-binding peptide
Beilstein J. Nanotechnol. 2023, 14, 280–290, doi:10.3762/bjnano.14.25
- and proteins, have been demonstrated to be useful in the synthesis and self-assembly of inorganic nanostructures. Herein, we describe a simple Stöber-based method wherein both the synthesis and the self-assembly of SiO2 nanoparticles can be facilitated by a silica-binding peptide (SiBP). We
- monodisperse nanoparticles and to modify the surface properties to fully exploit the advantages offered by self-assembly. Biomolecules, such as peptides and proteins, have been demonstrated to be useful in the synthesis and self-assembly of inorganic nanostructures [15][16]. Herein, we have investigated the
- behavior of biosilicification-related proteins (BSRPs), such as silicateins and silaffins. BSRPs facilitate the formation of inorganic silica structures in marine organisms [27][28]. It has been reported that isolated silicateins and silaffins or certain repeating motifs of these proteins can facilitate
Recent progress in cancer cell membrane-based nanoparticles for biomedical applications
Beilstein J. Nanotechnol. 2023, 14, 262–279, doi:10.3762/bjnano.14.24
- system (RES) or the mononuclear phagocytosis system (MPS) [4]. The subsequent rapid clearance from blood circulation by the liver and kidneys results in insufficient drug accumulation in the target tissue [5]. In addition, NPs can interact with proteins to form a protein corona, which affects the
- bioimaging of tumors. Finally, the prospects and challenges for the clinical translation of cancer cell membrane-mimetic NPs are discussed. 2 The functions of the cancer cell membrane Different types of proteins present in the cancer cell membrane affect the properties of cancer cells and the way they
- interact with other cells. The biological effects of nanoformulations can be enhanced through the effective utilization of specific protein groups. A schematic diagram of surface proteins and functions of the cancer cell membrane is shown in Figure 2. 2.1 Homologous targeting Cancer cells usually exhibit
Nanotechnology – a robust tool for fighting the challenges of drug resistance in non-small cell lung cancer
Beilstein J. Nanotechnol. 2023, 14, 240–261, doi:10.3762/bjnano.14.23
- growth factor inhibition in vitro, maintaining its biological efficacy in cells and xenograft models with different mutation statuses [70][72][73][74]. Further advances in the multimodal combination therapy approach KRAS proteins operate as guanosine diphosphate (GDP)/guanosine triphosphate (GTP
Antimicrobial and mechanical properties of functionalized textile by nanoarchitectured photoinduced Ag@polymer coating
Beilstein J. Nanotechnol. 2023, 14, 95–109, doi:10.3762/bjnano.14.11
- the bacterial cell membrane [19][20], allowing its penetration inside the cytoplasm. This leads to the leakage of cellular components through the pores of the perforated cellular membrane. Once inside, the ions promote reactive oxygen species (ROS) generation, deactivate proteins, and block DNA
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