Gotowe bibliografie tematyczne / Conjugated Biomolecules

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Gotowa bibliografia na temat „Conjugated Biomolecules”

Autor: Grafiati

Data publikacji: 7 września 2023

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Artykuły w czasopismach na temat "Conjugated Biomolecules"

Wang, Jian, Ting Ting Wang, Peng Fei Gao i Cheng Zhi Huang. "Biomolecules-conjugated nanomaterials for targeted cancer therapy". J. Mater. Chem. B 2, nr 48 (2014): 8452–65. http://dx.doi.org/10.1039/c4tb01263a.

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Now and in the future, with the development of artificial biomolecules as well as nanomaterials, targeted drug delivery based on elegant biomolecule–nanomaterial conjugation approaches is being developed to achieve great versatility, additional functions, and further advances.

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Park, Sinwook, Keren Buhnik-Rosenblau, Ramadan Abu-Rjal, Yechezkel Kashi i Gilad Yossifon. "Periodic concentration–polarization-based formation of a biomolecule preconcentrate for enhanced biosensing". Nanoscale 12, nr 46 (2020): 23586–95. http://dx.doi.org/10.1039/d0nr05930g.

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Periodic concentration–polarization-based formation of a preconcentrated biomolecule plug using the sandwich immunoassay approach, wherein the target biomolecules bind between immobilized magnetic bead-conjugated antibodies and reporter antibodies.

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Abes, S., H. Moulton, J. Turner, P. Clair, J. P. Richard, P. Iversen, M. J. Gait i B. Lebleu. "Peptide-based delivery of nucleic acids: design, mechanism of uptake and applications to splice-correcting oligonucleotides". Biochemical Society Transactions 35, nr 1 (22.01.2007): 53–55. http://dx.doi.org/10.1042/bst0350053.

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CPPs (cell-penetrating peptides) have given rise to much interest for the delivery of biomolecules such as peptides, proteins or ONs (oligonucleotides). CPPs and their conjugates were initially thought to translocate through the cell membrane by a non-endocytotic mechanism which has recently been re-evaluated. Basic-amino-acid-rich CPPs first interact with cell-surface proteoglycans before being internalized by endocytosis. Sequestration and degradation in endocytotic vesicles severely limits the cytoplasmic and nuclear delivery of the conjugated biomolecules. Accordingly, splicing correction by CPP-conjugated steric-block ON analogues is inefficient in the absence of endosomolytic agents. New arginine-rich CPPs allowing efficient splicing correction by conjugated PNAs (peptide nucleic acids) or PMO (phosphorodiamidate morpholino oligomer) steric blockers in the absence of endosomolytic agents have recently been defined in our group and are currently being characterized. They offer promising leads for the development of efficient cellular delivery vectors for therapeutic steric-block ON analogues.

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Ni, Jielei, Bo Cao, Gang Niu, Danni Chen, Guotao Liang, Tingying Xia, Heng Li i in. "Improved localization precision via restricting confined biomolecule stochastic motion in single-molecule localization microscopy". Nanophotonics 11, nr 1 (16.11.2021): 53–65. http://dx.doi.org/10.1515/nanoph-2021-0481.

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Abstract Single-molecule localization microscopy (SMLM) plays an irreplaceable role in biological studies, in which nanometer-sized biomolecules are hardly to be resolved due to diffraction limit unless being stochastically activated and accurately located by SMLM. For biological samples preimmobilized for SMLM, most biomolecules are cross-linked and constrained at their immobilizing sites but still expected to undergo confined stochastic motion in regard to their nanometer sizes. However, few lines of direct evidence have been reported about the detectability and influence of confined biomolecule stochastic motion on localization precision in SMLM. Here, we access the potential stochastic motion for each immobilized single biomolecule by calculating the displacements between any two of its localizations at different frames during sequential imaging of Alexa Fluor-647-conjugated oligonucleotides. For most molecules, localization displacements are remarkably larger at random frame intervals than at shortest intervals even after sample drift correction, increase with interval times and then saturate, showing that biomolecule stochastic motion is detected and confined around the immobilizing sizes in SMLM. Moreover, localization precision is inversely proportional to confined biomolecule stochastic motion, whereas it can be deteriorated or improved by enlarging the biomolecules or adding a post-crosslinking step, respectively. Consistently, post-crosslinking of cell samples sparsely stained for tubulin proteins results in a better localization precision. Overall, this study reveals that confined stochastic motion of immobilized biomolecules worsens localization precision in SMLM, and improved localization precision can be achieved via restricting such a motion.

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Katas, Haliza, Nik Nur Shamiha Nik Dzulkefli i Shariza Sahudin. "Synthesis of a New Potential Conjugated TAT-Peptide-Chitosan Nanoparticles Carrier via Disulphide Linkage". Journal of Nanomaterials 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/134607.

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Chitosan and TAT peptide have been widely investigated as delivery systems for various biomolecules such as plasmid DNA, oligonucleotides, and siRNAs. Conjugation of chitosan with TAT-peptide was therefore expected to produce a carrier with enhanced ability to facilitate cellular uptake. In this study, chitosan nanoparticles (CNs) were prepared by ionic gelation method prior to conjugation with TAT-peptide via disulphide linkage (CN-TAT). The conjugation was performed at various TAT-peptide-to-chitosan weight ratios ranging from 0.008 : 1 to 0.125 : 1. siRNA as a model biomolecule was loaded by adsorption onto the CN-TAT. Nanosize range particles were produced with a size range of less than 700 nm depending on TAT-peptide concentration used. HPLC and Raman spectrometry analysis revealed that TAT-peptide was successfully conjugated to the CN via disulphide linkage. siRNA loading efficiency for CN-TAT was 93% ±0.01.In vitrocytotoxicity studies showed that CN-TAT has relatively low toxicity. In conclusion, TAT conjugated onto CN via disulphide linkage was successfully synthesized, and its low cytoxicity demonstrates a potential for its use as a vector for biomolecules.

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Higashi, Sayuri L., Normazida Rozi, Sharina Abu Hanifah i Masato Ikeda. "Supramolecular Architectures of Nucleic Acid/Peptide Hybrids". International Journal of Molecular Sciences 21, nr 24 (12.12.2020): 9458. http://dx.doi.org/10.3390/ijms21249458.

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Supramolecular architectures that are built artificially from biomolecules, such as nucleic acids or peptides, with structural hierarchical orders ranging from the molecular to nano-scales have attracted increased attention in molecular science research fields. The engineering of nanostructures with such biomolecule-based supramolecular architectures could offer an opportunity for the development of biocompatible supramolecular (nano)materials. In this review, we highlighted a variety of supramolecular architectures that were assembled from both nucleic acids and peptides through the non-covalent interactions between them or the covalently conjugated molecular hybrids between them.

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Khatchadourian, Rafael, Alexia Bachir, Samuel J. Clarke, Colin D. Heyes, Paul W. Wiseman i Jay L. Nadeau. "Fluorescence Intensity and Intermittency as Tools for Following Dopamine Bioconjugate Processing in Living Cells". Journal of Biomedicine and Biotechnology 2007 (2007): 1–10. http://dx.doi.org/10.1155/2007/70145.

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CdSe/ZnS quantum dots (QDs) conjugated to biomolecules that quench their fluorescence, particularly dopamine, have particular spectral properties that allow determination of the number of conjugates per particle, namely, photoenhancement and photobleaching. In this work, we quantify these properties on a single-particle and ensemble basis in order to evaluate their usefulness as a tool for indicating QD uptake, breakdown, and processing in living cells. This creates a general framework for the use of fluorescence quenching and intermittency to better understand nanoparticle-cell interactions.

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Zhuravlova, Maryna, Nataliya Obernikhina, Stepan Pilyo, Maryna Kachaeva, Oleksiy Kachkovsky i Volodymyr Brovarets. "In silico binding affinity studies of phenyl-substituted 1,3-oxazoles with protein molecules". Ukr. Bioorg. Acta 2020, Vol. 15, N1 15, nr 1 (30.06.2020): 12–19. http://dx.doi.org/10.15407/bioorganica2020.01.012.

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The new model approach of interaction between the pharmacophores with bio-molecules, fragment-to-fragment, is presented. It is a new step of the molecular modeling and takes correctly into consideration not only the spatial complementarity of the interacted molecules but also the contribution of the stacking π-π-electron interaction and hydrogen bonds. As an example, the correct analysis of the interaction of the biological active phenyl-substituted 1,3-oxazoles with protein fragments is performed. It was shown that the length and energy of the hydrogen bond uniquely depend on the chemical constitution of both components in the created complex [Pharmacophore(Oxazole)-Biomolecule (H-X)]. The binding energy regularly decreases in the series X → O, S, NH (fragments of the corresponding biomolecules). It should be pointed out that introduction of the conjugated phenyl groups at positions 2 and 5 of oxazoles increase the stability of the possibly generated complex Pharmacophore-Biomolecule [Pharm-BioM] with fragments of the corresponding biomolecules along the core of oxazole by 0.2 and 0.5 kcal/mole. At the same time, modeling of the possibly generated complex [Pharm-BioM] by phenyl substituents at position 2 and 5 of 1,3-oxazole with phenylalanine as a fragment of protein molecules additionally stabilizes complex by 2.5 kcal/mole by π-stacking mechanism. It seems, the observed biological activity of the phenyl substituted 1,3-oxazole is rather connected with the possibility to generate the stable complex due to the formation of additional bonds with other fragments (conjugated phenyl core). The calculations give that such substituents do not cause spatial hindrances with the polypeptide chain.

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McKenzie, Fiona, Victoria Steven, Andrew Ingram i Duncan Graham. "Quantitation of biomolecules conjugated to nanoparticles by enzyme hydrolysis". Chemical Communications, nr 20 (2009): 2872. http://dx.doi.org/10.1039/b823057a.

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Yang, Meng, Susan Hoppmann, Luxi Chen i Zhen Cheng. "Human Serum Albumin Conjugated Biomolecules for Cancer Molecular Imaging". Current Pharmaceutical Design 18, nr 8 (1.03.2012): 1023–31. http://dx.doi.org/10.2174/138161212799315830.

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Rozprawy doktorskie na temat "Conjugated Biomolecules"

Wigenius, Jens. "Conjugated Polyelectrolytes in Interactions with Biomolecules for Supramolecular assembly and Sensing". Doctoral thesis, Linköpings universitet, Biomolekylär och Organisk Elektronik, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-54902.

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Conjugated polyelectrolytes (CP) show interesting electrical and optical properties for organic electronics as well as for life science applications. Their possibilities of supramolecular assembly with nanowire like misfolded proteins, amyloids, as well as synthetic polypeptides or DNA forming conducting or luminescent nano composites is highly interesting as being a truly bottom up approach for fabrication of OLEDs, photovoltaic’s as well as logic devices. The conformation and aggregation dependent luminescence properties from the special class of CPs, Luminescent conjugated polyelectrolytes (LCP), have been utilised and developed as sensors to follow and study biomolecular interactions, DNA hybridisation, protein-protein interactions and staining of living cell cultures and tissue slides. In this thesis we are bringing the evolution a few steps further by applying new types of experimental techniques, such as light scattering and fluorescence correlation spectroscopy, combined with standard techniques as soft lithography and different spectroscopy techniques, to gain better knowledge of the optical behaviour of LCPs and their interactions with biomolecules. We explore the optical properties and vibronic transitions of LCPs; their ability of resonance energy transfer with LCPs indicating super lightning behaviour; the opposite fluorescence shift when interacting with α-helical rich polypeptides compared to earlier reports of interactions upon staining of β-rich amyloids; and the possibility of LCPs to influence protein aggregation as well as the possibility of fabricating biochips based on LCPs and soft lithography. Here we also show fundamental limitations to patterning using macromolecular fluids, of general relevance to soft lithography and nanoimprint lithography with low viscosity polymers.

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Phillips, Ronald Lee III. "Poly(para-phenyleneethynylene)s probing the biological interface with biomolecular materials /". Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26555.

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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2009.
Committee Chair: Dr. Uwe H.F. Bunz; Committee Member: Dr. Andrew Lyon; Committee Member: Dr. Laren Tolbert; Committee Member: Dr. Nicholas Hud; Committee Member: Dr. Sherry Michele Owen. Part of the SMARTech Electronic Thesis and Dissertation Collection.

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Zhang, Yue. "Development of functional nanoparticle-biomolecule conjugates based biosensors". Thesis, University of Leeds, 2013. http://etheses.whiterose.ac.uk/4944/.

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This thesis is composed of two parts: Part I is focused on studying how quantum dot (QD) surface small-molecule capping ligands affect its Förster resonance energy transfer (FRET) with a fluorescent protein (FP); Part II is focused on developing an ultrasensitve DNA sensing technology by combining magnetic nanoparticle (MNP) and enzymatic signal amplification. Part I The FRET between a CdSe/ZnS core/shell QD capped with three different small-molecule ligands and a hexa-histidine (His6)-tagged FP (mCherry) has been studied. Results show that small-molecule ligands strongly affect the FRET behaviours between QD and FP. The QD-FP self-assembly process is fast (complete in minutes at low nM concentration), strong (with Kd ~ 1 nM), suggesting that the QD-His6-tagged biomolecule self-assembly is an effective approach for making compact QD-bioconjugates which may have a wide range of sensing and biomedical applications. PART II I have developed a facile, rapid, and sensitive DNA sensor by combining the efficient MNP-based target capture with the highly efficient signal amplification power of enzymes to achieve ultra-sensitivity. This sensor works efficiently in both pure buffer and complex media (such as 10% human serum in buffer). Moreover, this developed approach is able to quantitate two distinct DNA strands in a homogenous phase at the same time with a detection limit of ~5 pM. Second, I have developed a novel, highly sensitive and selective approach for label-free DNA detection and single-nucleotide polymorphism (SNP) discrimination by combining target-recycled ligation (TRL), MNP assisted target capture/ separation, and efficient enzymatic amplification. This approach possesses a detection limit of 600 fM unlabelled DNA targets and offers exquisitely high discrimination ratio (up to > 380 fold) between a perfect-match mutant and its single-base mismatch DNA target. Furthermore, it can quantitate the rare cancer mutant in large excesses of coexisting wildtype DNA down to 0.75%.

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Elfwing, Anders. "On decoration of biomolecular scaffolds with a conjugated polyelectrolyte". Doctoral thesis, Linköpings universitet, Biomolekylär och Organisk Elektronik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-141675.

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Biotemplating is the art of using a biological structure as a scaffold which is decorated with a functional material. In this fashion the structures will gain new functionalities and biotemplating offers a simple route of mass-producing mesoscopic material with new interesting properties. Biological structures are abundant and come in a great variety of elaborate and due to their natural origin they could be more suitable for interaction with biological systems than wholly synthetic materials. Conducting polymers are a novel class of material which was developed just 40 years ago and are well suited for interaction with biological material due to their organic composition. Furthermore the electronic properties of the conducting polymers can be tuned giving rise to dynamic control of the behavior of the material. Self-assembly processes are interesting since they do not require complicated or energy demanding processing conditions. This is particularly important as most biological materials are unstable at elevated temperatures or harsh environments. The main aim of this thesis is to show the possibility of using self-assembly to decorate a conducting polymer onto various biotemplates. Due to the intrinsic variety in charge, size and structure between the available natural scaffolds it is difficult, if not impossible, to find a universal method. In this thesis we show how biotemplating can be used to create new hybrid materials by self-assembling a conducting polymer with biological structures based on DNA, protein, lipids and cellulose, and in this fashion create material with novel optical and electronic properties.

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Herland, Anna. "Conjugated Polymers, Amyloid Detection and Assembly of Biomolecular Nanowires". Doctoral thesis, Linköping : Biomolecular and Organic Electronics, Department of Physics, Chemistry and Biology, Linköping University, 2007. http://www.bibl.liu.se/liupubl/disp/disp2007/tek1117s.pdf.

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Mekapothula, Swapna. "Gold nanoparticle-biomolecule conjugates synthesis, properties, cellular interactions and cytotoxicity studies /". Diss., Columbia, Mo. : University of Missouri-Columbia, 2008. http://hdl.handle.net/10355/5641.

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Thesis (M.S.)--University of Missouri-Columbia, 2008.
"May 2008" The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Includes bibliographical references.

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Ogbodu, Racheal O. "Photophysicochemical properties and in vitro photodynamic therapy activities of zinc phthalocyanine conjugates with biomolecules and single-walled carbon nanotubes". Thesis, Rhodes University, 2015. http://hdl.handle.net/10962/d1017924.

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The synthesis, photophysicochemcial properties, in vitro dark toxicity and photodynamic therapy (PDT) activities of different derivatives of zinc phthalocyanine (ZnPc) conjugates with biomolecules (folic acid, bovine serum albumin (BSA), ascorbic acid, uridine or spermine) and single-walled carbon nanotubes (SWCNTs) are presented in this work. The fluorescence quantum yields (ΦF) (Subscript F) of the ZnPc derivatives or ZnPc-biomolecule conjugates remained relatively the same as compared to the precursor Pcs. Slight increases were observed in the ΦF (Subscript F) values of conjugates containing substituents such as pyrene, folic acid or BSA with intrinsic fluorescence properties. The triplet quantum yield (ΦT ) (Subscript T) values for some ZnPc conjugates increases compared to the precursor ZnPcs due to extended π conjugation (for the conjugate with pyrene) and the presence of phenyl ring that support spin-orbit charge transfer intersystem crossing to triplet state. While some conjugates showed decreases in the ΦT (Subscript T) values compared to precursor ZnPcs due to the presence of substituents that could quench photo-excited state properties. The singlet oxygen quantum yield (ΦΔ ) values follow the trends of the triplet quantum yield values. The conjugates containing BSA also show increases in the ΦΔ values without corresponding increases in ΦT (Subscript T) values due to the ability of BSA to generate free radicals including singlet oxygen. The presence of SWCNTs decreases the photophysicochemcial properties of some ZnPc-SWCNT conjugates compared to the precursor ZnPcs due to photo-induced electron transfer from an excited Pc complex (electron donor) to SWCNTs (electron acceptor). However, increases were observed in some ZnPc-SWCNT conjugates as a result of fast charge recombination process due to highly short-lived radical ion pair produced. These phenomena affected the ΦF (Suscript F) values, ΦT (Suscript T) values, and the ΦΔ values. Increases or decreases in ΦT (Suscript T) values resulted in corresponding increases or decreases in ΦΔ values

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Winger, Theodore Medard. "Synthetic phospholipid-peptide conjugates : biomolecular building blocks for receptor activating structures". Thesis, Georgia Institute of Technology, 1994. http://hdl.handle.net/1853/9505.

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Maione, Silvana. "Polymers and peptide-polymer conjugates as bioactive platforms and carriers for the encapsulation of biomolecules". Doctoral thesis, Universitat Politècnica de Catalunya, 2017. http://hdl.handle.net/10803/460833.

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In the last decade, conductive polymers have received great interest in both scientific and technological levels due to the electroactive properties exhibited by these materials. For this reason, the main aim of this Doctoral Thesis is to study the applications of some conducting polymers, mainly derived from polythiophene, in the field of biomedicine and biotechnology. According to the objectives proposed in this Document, different studies focused on the preparation and characterization of graft copolymers have been carried out using macromonomers formed by oligo-thiophenes to which PEG chains of well-defined molecular weight have been incorporated as substituents. After this, the behavior of these new polymers has been investigated in terms of cytotoxicity and biocompatibility using cell adhesion and cell proliferation assays. Then, the synthesis and characterization of conducting polymer-peptide hybrids have been developed. Initially, the methodology used for the preparation of these materials has been optimized using model systems in which the peptide has been replaced by an amino acid, which has been engineered by chemical similarity. After evaluate different synthetic approaches, hybrids constructed by combining the same conducting polymer and the RG*D peptide have been prepared, where RG*D is a sequence analogous to the RGD (Arg-Gly-Asp) in which the central Gly residue is replaced by the above mentioned engineered amino acids. The biocompatibility and the bioactivity of all these compounds have been examined. The last part of this thesis is oriented towards the encapsulation of small biomolecules in polymeric nanostructures that can be used as transport systems and controlled release systems when incorporated into the organism. The encapsulation of simple amino acids has been examined firstly, this research evolving towards the immobilization of linear and cyclic hydrophobic peptides. In all cases encapsulation was carried out by electrospraying or electrospinning.
En la última década, los polímeros conductores han despertado un gran interés tanto a nivel científico como tecnológico debido a las propiedades electroactivas que exhiben estos materiales. Por este motivo, en la presente Tesis Doctoral se han estudiado las aplicaciones de algunos de estos polímeros conductores, principalmente derivados del politiofeno, en el ámbito de la biomedicina y la biotecnología. Según los objetivos propuestos en esta Memoria, inicialmente se han realizado estudios relacionados con la preparación y caracterización de copolímeros de injerto empleando macromonómeros formados por oligotiofenos, a los que se les ha incorporado una cadena de polietilenglicol de peso molecular definido. Seguidamente se ha investigado su comportamiento mediante ensayos de citotoxicidad, adhesión celular y proliferación celular. A continuación, se ha realizado la síntesis y la caracterización de híbridos polímero conductor-péptido. Inicialmente, se ha optimizado el método de preparación de estos materiales empleando sistemas modelo, en los que el péptido ha sido re-emplazado por un amino ácido diseñado por similaridad química. Una vez evaluadas las diferentes estrategias sintéticas, se han obtenido híbridos formados por el mismo polímero y el péptido RG*D, donde RG*D es una secuencia análoga a la RGD (Arg-Gly-Asp) en la que el residuo central se ha sustituido por el amino ácido mencionado anteriormente. Para estos materiales se ha evaluado la biocompatibilidad y la bioactividad. La última parte de esta Tesis está orientada a la encapsulación de biomoléculas de pequeño tamaño en nanoestructuras poliméricas que pueden ser empleadas como sistemas transportadores y sistemas de liberación controlada cuando se incorporan al organismo. Los estudios se han iniciado encapsulando diferentes amino ácidos y se han acabado con péptidos hidrofóbicos lineales y cíclicos. En todos los casos la encapsulación se ha llevado a cabo mediante electrospraying o electrospinning.

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Stumper, Anne [Verfasser]. "Designing potent PDT drug candidates - development of crucial linking strategies for biomolecule-metal-complex-conjugates / Anne Stumper". Ulm : Universität Ulm, 2018. http://d-nb.info/1150301856/34.

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Książki na temat "Conjugated Biomolecules"

Noble Metal Nanoparticlesbiomolecules Conjugates. John Wiley & Sons Inc, 2014.

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Części książek na temat "Conjugated Biomolecules"

Barbatti, Mario, Matthias Ruckenbauer, Jaroslaw J. Szymczak, Bernhard Sellner, Mario Vazdar, Ivana Antol, Mirjana Eckert-Maksić i Hans Lischka. "Model Systems for Dynamics of π-Conjugated Biomolecules in Excited States". W Handbook of Computational Chemistry, 1175–213. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-0711-5_33.

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Barbatti, Mario, Matthias Ruckenbauer, Jaroslaw J. Szymczak, Bernhard Sellner, Mario Vazdar, Ivana Antol, Mirjana Eckert-Maksić i Hans Lischka. "Model Systems for Dynamics of π-Conjugated Biomolecules in Excited States". W Handbook of Computational Chemistry, 1–43. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-007-6169-8_33-2.

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Barbatti, Mario, Matthias Ruckenbauer, Jaroslaw J. Szymczak, Bernhard Sellner, Mario Vazdar, Ivana Antol, Mirjana Eckert-Maksić i Hans Lischka. "Model Systems for Dynamics of π-Conjugated Biomolecules in Excited States". W Handbook of Computational Chemistry, 1697–739. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-27282-5_33.

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van de Plas, F. E. M. Peter, i Jan L. M. Leunissen. "Colloidal Gold as a Marker in Molecular Biology: The Use of Ultra-Small Gold Conjugates". W Nonradioactive Analysis of Biomolecules, 193–205. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57206-7_11.

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Choy, Jin Ho, Jae Min Oh i Soo Jin Choi. "Nanoceramics-Biomolecular Conjugates for Gene and Drug Delivery". W Advances in Science and Technology, 769–78. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/3-908158-01-x.769.

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Galibert, Mathieu, Olivier Renaudet, Didier Boturyn i Pascal Dumy. "Preparation of Peptide and Other Biomolecular Conjugates Through Chemoselective Ligations". W Methods in Molecular Biology, 67–79. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-151-2_6.

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Capek, Ignac. "Dispersions Based on Carbon Nanotubes – Biomolecules Conjugates". W Carbon Nanotubes - Growth and Applications. InTech, 2011. http://dx.doi.org/10.5772/18583.

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"Water-Soluble Biomolecules, Synthetic Polymers, and their Conjugates". W Polymer Biomaterials in Solution, as Interfaces and as Solids, 863–986. CRC Press, 2014. http://dx.doi.org/10.1201/b12021-17.

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Neuditschko, Benjamin, Bernhard K. Keppler, Christopher Gerner i Samuel M. Meier-Menches. "Organometallic Receptors and Conjugates With Biomolecules in Bioorganometallic Chemistry". W Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-820206-7.00054-8.

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Sudhaharan, Thankiah, i Annadi Ram Reddy. "Assay of Diversified Biomolecules with a Luminogenic Conjugate Substrate". W Luminescence Biotechnology, 131–43. CRC Press, 2001. http://dx.doi.org/10.1201/9781420041804.ch8.

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Streszczenia konferencji na temat "Conjugated Biomolecules"

Karunanithy, Robinson, P. Sivakumar i Torrey Holland. "IDENTIFYING THE DIFFERENCES IN CONJUGATED VS. NON-CONJUGATED BIOMOLECULES IN CANCER RESEARCH USING VIBRATIONAL SPECTROSCOPY". W 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.wi01.

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Nilsson, K. Peter R. "Luminescent conjugated oligothiophenes: real time in vivo imaging of biomolecules". W SPIE Photonic Devices + Applications, redaktorzy Ruth Shinar i George G. Malliaras. SPIE, 2009. http://dx.doi.org/10.1117/12.825655.

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McMahon, Nathan, Jocelyn Jones, Jennifer Eng, Sunjong Kwon, Young Hwan Chang, Guillaume Thibault, Koei Chin, Michel Nederlof, Joe Gray i Summer Gibbs. "Signal removal methods for highly multiplexed immunofluorescent staining using antibody conjugated oligonucleotides". W Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XVII, redaktorzy Daniel L. Farkas, James F. Leary i Attila Tarnok. SPIE, 2019. http://dx.doi.org/10.1117/12.2510573.

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Savitsky, Alexander P., K. V. Lopatin, Oleg I. Lobanov, N. A. Golubeva, Marina Y. Poroshina, Elena B. Chernyaeva, L. I. Solovieva i in. "Photophysical properties of protein conjugates with PDT photosensitizers". W Laser Spectroscopy of Biomolecules: 4th International Conference on Laser Applications in Life Sciences, redaktor Jouko E. Korppi-Tommola. SPIE, 1993. http://dx.doi.org/10.1117/12.146207.

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Licha, Kai, Andreas Becker, Frank Kratz i Wolfhard Semmler. "New contrast agents for optical imaging: acid-cleavable conjugates of cyanine dyes with biomolecules". W BiOS '99 International Biomedical Optics Symposium, redaktorzy Darryl J. Bornhop, Christopher H. Contag i Eva M. Sevick-Muraca. SPIE, 1999. http://dx.doi.org/10.1117/12.351013.

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Pauli, J., R. Brehm, M. Grabolle, T. Behnke, J. Mathejczyk, F. Hamann, F. Alves, I. Hilger i U. Resch-Genger. "Dye-biomolecule conjugates and NIR-fluorescent particles for targeting of disease-related biomarkers". W SPIE BiOS, redaktorzy Samuel Achilefu i Ramesh Raghavachari. SPIE, 2011. http://dx.doi.org/10.1117/12.876828.

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Alper, Joshua, i Kimberly Hamad-Schifferli. "Biomolecular Activity Switch: An Application of Metallic Nanoparticle Plasmon Resonance and Femtosecond Pulsed Lasers". W ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-68104.

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Streszczenie:

With an increased effort within the engineering community to design molecular machines, it has become clear that a specific, external control method is required. Here we propose a simple mechanism for a molecular switch involving conjugating a molecule within the machinery to a gold nanorod. Then actuate that machinery’s active state by affecting a change in the conjugated molecule. We demonstrate the feasibility of the method using a fluorescent probe, and we report on progress we have made toward demonstrating it with a protein.

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