Fluorescent bioinspired albumin/polydopamine nanoparticles and their interactions with Escherichia coli cells

• Eloïse Equy,
• Jordana Hirtzel,
• Sophie Hellé,
• Béatrice Heurtault,
• Eric Mathieu,
• Morgane Rabineau,
• Vincent Ball and
• Lydie Ploux

Beilstein J. Nanotechnol. 2023, 14, 1208–1224, doi:10.3762/bjnano.14.100

• applications, especially because of their biocompatibility. We synthesized and characterized fluorescent PDA NPs of 10–25 nm diameter based on a protein containing a lysine–glutamate diad (bovine serum albumin, BSA) and determined whether they can penetrate and accumulate in bacterial cells to serve as a

• additive plays a crucial role in the control of the NP size. Specifically, Bergtold et al. demonstrated that a protein (e.g. chromofungin) containing a diad of lysine (K) and glutamate (E) (Figure 1a,b) in its sequence allows for the control of the formation of PDA NPs, in contrast to an additive without a

• KE diad (e.g., catestatin) [13]. During the formation process, hydroxy groups of dopamine form hydrogen bonds with carboxylic groups (COO−) of glutamate (pKa = 4.3), whereas protonated amino groups (NH3+) of lysine (pKa = 10.5) further stabilize the aggregate by cation–π interactions with the

Green SPIONs as a novel highly selective treatment for leishmaniasis: an in vitro study against Leishmania amazonensis intracellular amastigotes

• Brunno R. F. Verçoza,
• Robson R. Bernardo,
• Luiz Augusto S. de Oliveira and
• Juliany C. F. Rodrigues

Beilstein J. Nanotechnol. 2023, 14, 893–903, doi:10.3762/bjnano.14.73

• promastigotes (control and treated cells) were washed in phosphate-buffered saline (PBS) pH 7.2 and adhered for 10 min on glass coverslips previously coated with poly-ʟ-lysine (Sigma-Aldrich, Germany). The intracellular amastigotes were obtained after infection of RAW 264.7 macrophages at a ratio of ten

Polymer nanoparticles from low-energy nanoemulsions for biomedical applications

• Santiago Grijalvo and
• Carlos Rodriguez-Abreu

Beilstein J. Nanotechnol. 2023, 14, 339–350, doi:10.3762/bjnano.14.29

• synthesis of polyurethane and polyurea from the reaction of poly(ethyleneglycol) or lysine with isophorone diisocyanate (IPDI) [68][69]. Nanoemulsions were prepared using Polysorbate 80 as surfactant, medium-chain triglycerides as the oil phase (O/S ratio from 10/90 to 30/70), and 90 wt % of aqueous phase

• content is not subject to CC BY 4.0. TEM images and corresponding size distributions of (a) PEGylated polyurethane and (b) lysine-coated polyurea nanocapsules obtained from O/W nanoemulsions in an aqueous solution/polysorbate 80/medium chain triglyceride/diisocyanate system at O/S = 10/90 and 90 wt % of

Cyclodextrins as eminent constituents in nanoarchitectonics for drug delivery systems

• Makoto Komiyama

Beilstein J. Nanotechnol. 2023, 14, 218–232, doi:10.3762/bjnano.14.21

• transferrin (tumor-targeting protein) which bears poly(ʟ-lysine), mitochondrion-targeting peptide, poly(ethylene glycol), and arylazopyrazole (trans isomer) [89]. Under irradiation with NIR light (808 nm), the photothermal effect disrupted mitochondrial function, leading to inhibition of tumor growth. 6 Some

Recent advances in green carbon dots (2015–2022): synthesis, metal ion sensing, and biological applications

• Aisha Kanwal,
• Naheed Bibi,
• Sajjad Hyder,
• Arif Muhammad,
• Hao Ren,
• Jiangtao Liu and
• Zhongli Lei

Beilstein J. Nanotechnol. 2022, 13, 1068–1107, doi:10.3762/bjnano.13.93

• as a dual sensor for tetracycline and ʟ-lysine. The fluorescence of CDs is quenched by adding tetracycline and regained by introducing ʟ-lysine [18]. Palmyra leaves were utilized by Athinarayanan et al. for the production of CDs. The cellular toxicity of the CDs was analyzed, and the CDs were found

Biomimetic chitosan with biocomposite nanomaterials for bone tissue repair and regeneration

• Se-Kwon Kim,
• Sesha Subramanian Murugan,
• Pandurang Appana Dalavi,
• Sebanti Gupta,
• Sukumaran Anil,
• Gi Hun Seong and
• Jayachandran Venkatesan

Beilstein J. Nanotechnol. 2022, 13, 1051–1067, doi:10.3762/bjnano.13.92

• weeks. The emergence of new bone in the defective region is confirmed by microscale computational micrographs and staining assay findings [98]. Ning et al. (2019) developed glycyl-ʟ-histidyl-ʟ-lysine-containing copper ions integrated with mesoporous silica nanoparticles (MSN) and chitosan. Further, the

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

• proteins (HDPs) was coined [89]. HDPs are rich in cationic amino acids (e.g., arginine and lysine), and amino acids with hydrophobic side chains (e.g., tryptophan, phenylalanine, tyrosine, leucine, isoleucine, and valine). This composition renders them amphiphilic, which is crucial to their mode of action

• amino acid yielded a positively charged eADF4(κ16) and an uncharged eADF4(Ω16) variant, where the glutamic acid residue is exchanged with a lysine or glutamine residue, respectively [144][145][146]. The dragline silk of Nephila clavipes inspired the recombinant spider silk proteins 6mer and 15mer, in

• not allow good and sufficient cell attachment necessary for tissue engineering applications. However, several independent studies showed that the materials made of the positively charged eADF4(κ16) variant enabled partial cell adhesion due to the positive surface charge derived from lysine residues in

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

• from −14.89 to −20.25 mV showing a slight increase for particles crosslinked for a longer time. This can be explained by the consumption of lysine groups during the crosslinking process, resulting in less positively charged functional groups. The loading of FITC-dextran did not influence either size or

• nanoparticles. Crosslinking degree Glutaraldehyde is a frequently used crosslinker in the preparation of GNPs. Each molecule of glutaraldehyde reacts with two free amine groups [25]. Translating this to gelatin, it randomly reacts with the free aliphatic amine of lysine side chains. Therefore, it is appropriate

• to quantify the degree of crosslinking by determining free lysine in the particles. Colorimetric determination with trinitrobenzenesulfonic acid (TNBS) is a common method [26]. Under alkaline conditions, the primary amines and TNBS react to trinitrophenyl derivatives and sulfite. The formed compound

Stimuli-responsive polypeptide nanogels for trypsin inhibition

• Petr Šálek,
• Jana Dvořáková,
• Sviatoslav Hladysh,
• Diana Oleshchuk,
• Ewa Pavlova,
• Jan Kučka and
• Vladimír Proks

Beilstein J. Nanotechnol. 2022, 13, 538–548, doi:10.3762/bjnano.13.45

• biocompatible Nα-ʟ-lysine-grafted α,β-poly[(2-propyne)-ᴅ,ʟ-aspartamide-ran-(2-hydroxyethyl)-ᴅʟ-aspartamide-ran-(2-(4-hydroxyphenyl)ethyl)-ᴅʟ-aspartamide] (Nα-Lys-NG). Both nanogels were prepared by HRP/H2O2-mediated crosslinking in inverse miniemulsions with pH and temperature-stimuli responsive behavior

• ) (PLGA) nanoparticles loaded with AAT were successfully manufactured and AAT release profiles from the nanoparticles were investigated [21][22]. In our previous studies, we investigated and described in detail the process of nanogelation from Nα-ʟ-lysine-grafted α,β-poly[(2-propyne)-ᴅ,ʟ-aspartamide-ran

• comparison to PHEG-Tyr nanogel due to the presence of carboxyl groups of lysine in side chains of the zwitterionic Nα-Lys-NG nanogel [25][29]. The zeta potential of Nα-Lys-NG nanogel was not significantly affected by the change of temperature (Figure 3b). However, a slight decrease of zeta potential with

Micro- and nanotechnology in biomedical engineering for cartilage tissue regeneration in osteoarthritis

• Zahra Nabizadeh,
• Mahmoud Nasrollahzadeh,
• Hamed Daemi,
• Mohamadreza Baghaban Eslaminejad,
• Ali Akbar Shabani,
• Mehdi Dadashpour,
• Majid Mirmohammadkhani and
• Davood Nasrabadi

Beilstein J. Nanotechnol. 2022, 13, 363–389, doi:10.3762/bjnano.13.31

• ) (PLGA) microspheres coated with TGF-β3 loaded heparin/poly(ʟ-lysine) NPs showed extended growth factor release for 28 days and were found to be excellent structures for cell adhesion and chondrogenic differentiation [27]. Apart from serving as cell adhesion platforms and growth factor supplements

• for growth factor delivery systems. In this regard, the complexation of cationic polymers such as Pluronic F68 [56], polyethyleneimine (PEI) [57], and poly-ʟ-lysine [58] with anionic heparin has been widely used to promote ionic interactions for the preparation of growth factor-loaded NPs. Heparin

Systematic studies into uniform synthetic protein nanoparticles

• Nahal Habibi,
• Ava Mauser,
• Jeffery E. Raymond and
• Joerg Lahann

Beilstein J. Nanotechnol. 2022, 13, 274–283, doi:10.3762/bjnano.13.22

• cone, directed to a grounded substrate positioned below the cone. The ejected material dissociated into nanodroplets. After rapid solvent evaporation and solidification of non-volatile components, solid nanoparticles were deposited on the substrate. The reaction between lysine groups and NHS ester

Self-assembly of amino acids toward functional biomaterials

• Huan Ren,
• Lifang Wu,
• Lina Tan,
• Yanni Bao,
• Yuchen Ma,
• Yong Jin and
• Qianli Zou

Beilstein J. Nanotechnol. 2021, 12, 1140–1150, doi:10.3762/bjnano.12.85

• Fmoc groups, Fmoc-lysine and Fmoc-aspartic acid, by two-step self-assembly, which had an ultra-low critical gelling concentration and good mechanical properties and can be used for 2D/3D cell scaffolds and the production of conductive soft composites. In addition, Fmoc-amino acids can be co-assembled

• PS to tumor tissues [76]. Liu et al. [78] designed photosensitizer delivery systems by self-assembling cationic diphenylalanine (H-Phe-Phe-NH2 HCl, CDP) or 9-fluorenylmethoxycarbonyl-ʟ-lysine (Fmoc-ʟ-Lys) with Ce6 into nanoparticles (CCNPs and FCNPs, respectively). Intermolecular hydrophobic and π–π

• biomolecules, such as proteins, peptides, and DNA have received extensive attention in recent years [86]. Liu et al. [87] used electrostatic force to adsorb tetrakis(4-sulfonatophenyl)porphine (TPPS) molecules on the surface of 9-fluorenylmethoxycarbonyl-ʟ-lysine (Fmoc-ʟ-Lys) self-assembled nanofibers such

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

Fate and transformation of silver nanoparticles in different biological conditions

• Barbara Pem,
• Marija Ćurlin,
• Darija Domazet Jurašin,
• Valerije Vrček,
• Rinea Barbir,
• Vedran Micek,
• Raluca M. Fratila,
• Jesus M. de la Fuente and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2021, 12, 665–679, doi:10.3762/bjnano.12.53

• absorption spectroscopy (GF-AAS), nuclear magnetic resonance (NMR) spectroscopy, and transmission electron microscopy (TEM) experiments. Physicochemical characteristics of freshly prepared AgNPs Freshly prepared AgNPs coated with PVP, sodium bis(2-ethylhexyl)sulfosuccinate (AOT), and poly(ʟ-lysine) (PLL

On the stability of microwave-fabricated SERS substrates – chemical and morphological considerations

• Limin Wang,
• Aisha Adebola Womiloju,
• Christiane Höppener,
• Ulrich S. Schubert and
• Stephanie Hoeppener

Beilstein J. Nanotechnol. 2021, 12, 541–551, doi:10.3762/bjnano.12.44

• additives to fabricate uniform Ag nanoparticles. These include basic aminoacids (such as ʟ-lysine or ʟ-arginine) and soluble starch or other additives, which act as reducing and protecting agents, respectively [22]. In our approach, the monolayer of silver nanoparticles is formed by the reduction of silver

The impact of molecular tumor profiling on the design strategies for targeting myeloid leukemia and EGFR/CD44-positive solid tumors

• Nikola Geskovski,
• Nadica Matevska-Geshkovska,
• Simona Dimchevska Sazdovska,
• Marija Glavas Dodov,
• Kristina Mladenovska and
• Katerina Goracinova

Beilstein J. Nanotechnol. 2021, 12, 375–401, doi:10.3762/bjnano.12.31

• articles regarding the use of EGFR mAbs as a specific targeting motif for polymer NPs such as poly(lactic acid-co-lysine), poly(ethylene glycol-co-caprolactone), an poly(lactic acid-co-glycolic acid) NPs. All of them have shown

Fusion of purple membranes triggered by immobilization on carbon nanomembranes

• René Riedel,
• Natalie Frese,
• Fang Yang,
• Martin Wortmann,
• Raphael Dalpke,
• Daniel Rhinow,
• Norbert Hampp and
• Armin Gölzhäuser

Beilstein J. Nanotechnol. 2021, 12, 93–101, doi:10.3762/bjnano.12.8

• , the sample was rinsed with ethanol and dried in a stream of nitrogen. The sample was further functionalized by immersion in 1 mg of N-[N,N-bis(carboxymethyl)-ʟ-lysine]-12-mercaptododecan-amide (≥90%, Sigma-Aldrich) in 15 mL dried DMF solution. The sample was stored protected from light for 24 h

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

• ) esters as the copolymer. The NHS esters react with the lysine groups of BSA and polymerize into insoluble SPNPs. The SPNPs had a spherical shape according to SEM images. We further analyzed the size distribution of the particles using the ImageJ software and found that the particles had an average

• copolymer react with lysine groups in the proteins, the nanoparticles were placed in a dry oven at 37 °C for 7 days. All SPNP synthesis reagents were purchased from Sigma-Aldrich and Fisher Scientific. After polycondensation, the particles were collected by scraping them off the collecting surface using a

Applications of superparamagnetic iron oxide nanoparticles in drug and therapeutic delivery, and biotechnological advancements

• Maria Suciu,
• Corina M. Ionescu,
• Alexandra Ciorita,
• Septimiu C. Tripon,
• Dragos Nica,
• Hani Al-Salami and
• Lucian Barbu-Tudoran

Beilstein J. Nanotechnol. 2020, 11, 1092–1109, doi:10.3762/bjnano.11.94

• , dendrimers, albumin, silicones, liposomes, poloxamer, poly-ʟ-lysine, sugars, or polyethylene glycol (PEG) [27][28][29][30][31][32][33]. Hyperthermia treatment for cancer therapy is still under scrutiny. It shows great potential due to the property of SPIONs to produce local heat when placed under an

Multilayer capsules made of weak polyelectrolytes: a review on the preparation, functionalization and applications in drug delivery

• Varsha Sharma and
• Anandhakumar Sundaramurthy

Beilstein J. Nanotechnol. 2020, 11, 508–532, doi:10.3762/bjnano.11.41

• microparticles (10–200 µm) fabricated via stop flow lithography have emerged as useful templates to form custom-shaped and flexible microcapsules of poly-ʟ-lysine (PLL) [36]. The shell was formed by diffusion of PLL into an oppositely charged hydrogel matrix, enabling an easy surface modification that can be

• cell line showed a rapid uptake, demonstrating the potential for cancer therapy. Silica and gold NPs were assembled in a one pot assembly of specifically tailored diblock polymers of PLL and poly-ʟ-cysteine [82]. The electrostatic binding between the positively charged lysine blocks and negatively

Poly(1-vinylimidazole) polyplexes as novel therapeutic gene carriers for lung cancer therapy

• Gayathri Kandasamy,
• Elena N. Danilovtseva,
• Vadim V. Annenkov and
• Uma Maheswari Krishnan

Beilstein J. Nanotechnol. 2020, 11, 354–369, doi:10.3762/bjnano.11.26

• systems have emerged as a front-runner for gene delivery applications due to their polycationic nature, biocompatibility as well as the ability to escape the endosome by activating the proton sponge mechanism. In an earlier report, histidylated poly(ʟ-lysine) was found to exhibit high transfection

• -vinylimidazole) chains modified with aminoethyl groups demonstrated excellent DNA binding ability in synergy with lactosylated poly(ʟ-lysine). This system was found to exhibit excellent gene transfection ability specifically in hepatocytes through interactions with the asialoglycoprotein receptor expressed on

• the hepatocyte surface through the lactosylated poly(ʟ-lysine). The endosomal escape was mediated through a pH-responsive protonation of the imidazole and amino moieties that disrupted the endosomal membrane [17]. Zinc–PVI systems have also been investigated for complexing DNA for gene delivery

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

• different from hydrophobic interactions have been proposed. For example, electrostatic interactions can improve the photosensitizer loading. Mostly amino acid-based polymers with poly(ʟ-lysine) [46][47] or poly(aspartic acid) [48][49] charged blocks have been employed for poly ion complex assemblies (PICs

• reactive amine bonds. Not all of the lysine units should be modified to guarantee water solubility and enzymatic activation [83]. PEGylation could also improve solubility, but it was also proved to be detrimental regarding quenching [84]. More recently, polysaccharides based on chitosan or heparin have

Internalization mechanisms of cell-penetrating peptides

• Ivana Ruseska and
• Andreas Zimmer

Beilstein J. Nanotechnol. 2020, 11, 101–123, doi:10.3762/bjnano.11.10

• secondary amphipathic CPPs are the proline-rich peptides [7]. Nonamphipathic peptides are rather short peptides, such as HIV-TAT, which have a high content of positively charged amino acids such as arginine or lysine. Studies suggest that at least eight positive charges are necessary for efficient uptake to

• lysine, derived from the nuclear localization sequence (NLS) of SV-40 large T antigen, necessary for improving the solubility and the intracellular localization of the peptide and (iii) a spacer domain, which improves the flexibility. It has been reported by Deshayes et al. [29] that the internalization

• their stability and cellular uptake. MPG bears three domains: (i) a hydrophobic domain derived from the fusion domain of HIV-1 gp41, (ii) a lysine-rich nuclear localization sequence (NLS) derived from SV-40 large T antigen with five positive charges and (iii) a spacer sequence. Studies performed at low

Fully amino acid-based hydrogel as potential scaffold for cell culturing and drug delivery

• Dávid Juriga,
• Evelin Sipos,
• Orsolya Hegedűs,
• Gábor Varga,
• Miklós Zrínyi,
• Krisztina S. Nagy and
• Angéla Jedlovszky-Hajdú

Beilstein J. Nanotechnol. 2019, 10, 2579–2593, doi:10.3762/bjnano.10.249

• and the biodegradability of the hydrogel. In this paper, PASP cross-linked with cystamine (CYS) and lysine-methylester (LYS) was introduced as fully amino acid-based polymer hydrogel. Gels were synthesized employing six different ratios of CYS and LYS. The pH dependent swelling degree and the

• reductive conditions resulted in an increased drug release due to the cleavage of disulfide bridges in the hydrogels. Consequently, these hydrogels provide new possibilities in the fields of both tissue engineering and controlled drug delivery. Keywords: biocompatibility; cystamine; hydrogel; lysine; poly

• (amino acid)s [28][29]. The effect of poly-ʟ-lysine, which has a cationic character, on the cell behavior has been widely studied in the field of tissue engineering [30][31], while among the anionic poly(amino acid)s, poly(glutamic acid) is typically used for the development of hydrogel scaffolds [32

Evaluation of click chemistry microarrays for immunosensing of alpha-fetoprotein (AFP)

• Seyed Mohammad Mahdi Dadfar,
• Sylwia Sekula-Neuner,
• Vanessa Trouillet,
• Hui-Yu Liu,
• Ravi Kumar,
• Annie K. Powell and
• Michael Hirtz

Beilstein J. Nanotechnol. 2019, 10, 2505–2515, doi:10.3762/bjnano.10.241

• reagents are the simplest and most frequently used reagents for labeling proteins like antibodies. Within a pH range of 7–9, succinimidyl-ester reacts efficiently with the primary amino groups (–NH2) in the side chain of the lysine (K) residues of proteins to form stable amide bonds. This reaction results