Relevant bibliographies by topics / Biomacromolecules

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Biomacromolecules'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 September 2023

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Journal articles on the topic "Biomacromolecules"

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Sequeira, Rosy Alphons, Jitkumar Bhatt, and Kamalesh Prasad. "Recent Trends in Processing of Proteins and DNA in Alternative Solvents: A Sustainable Approach." Sustainable Chemistry 1, no. 2 (August 25, 2020): 116–37. http://dx.doi.org/10.3390/suschem1020010.

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Throughout numerous research works on biomacromolecules, several breakthrough innovations have occurred in the field of biomacromolecule processing. Remarkable improvements have been made so far to address the problems associated with biomacromolecule processing technologies in terms of enhancing the efficiency of the processes. Green technology broadly focuses on the search for new techno-economic systems to replace the conventional systems which exhibit pernicious consequences for the environment and the health of organisms. The strategy practiced popularly is the use of alternate solvent systems, replacing the conventional toxic, volatile, and harsh organic solvents to prevent denaturation, biotransformation, enzyme activity loss, and degradation of biomacromolecules. Ionic liquids (ILs) and deep eutectic solvents (DESs) are emerging as greener alternatives over the past two decades and there has been an exponential increase in reports in the literature. The utility of neoteric solvents in biomacromolecule treatment may be envisaged for industrial processes in the near future. The current state of the art regarding the recent developments made over the past few years using neoteric solvents has been reviewed in this article. The recent scientific developments regarding the use of these neoteric solvents, especially ILs and DESs, for processes such as solubilization, extraction, and functionalization of biomacromolecules, especially proteins and DNA, have been addressed in this article. This review may be beneficial for designing novel and selective methodologies for the processing of biomacromolecules, opening doors for better material research in areas such as biotechnology and biological sciences.
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Pleshakova, Tatyana O., Yuri D. Ivanov, Anastasia A. Valueva, Victoria V. Shumyantseva, Ekaterina V. Ilgisonis, Elena A. Ponomarenko, Andrey V. Lisitsa, Vladimir P. Chekhonin, and Alexander I. Archakov. "Analysis of Single Biomacromolecules and Viruses: Is It a Myth or Reality?" International Journal of Molecular Sciences 24, no. 3 (January 18, 2023): 1877. http://dx.doi.org/10.3390/ijms24031877.

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The beginning of the twenty-first century witnessed novel breakthrough research directions in the life sciences, such as genomics, transcriptomics, translatomics, proteomics, metabolomics, and bioinformatics. A newly developed single-molecule approach addresses the physical and chemical properties and the functional activity of single (individual) biomacromolecules and viral particles. Within the alternative approach, the combination of “single-molecule approaches” is opposed to “omics approaches”. This new approach is fundamentally unique in terms of its research object (a single biomacromolecule). Most studies are currently performed using postgenomic technologies that allow the properties of several hundreds of millions or even billions of biomacromolecules to be analyzed. This paper discusses the relevance and theoretical, methodological, and practical issues related to the development potential of a single-molecule approach using methods based on molecular detectors.
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Zhang, Huifeng, Yanfei Zhang, Chuang Zhang, Huan Yu, Yinghui Ma, Zhengqiang Li, and Nianqiu Shi. "Recent Advances of Cell-Penetrating Peptides and Their Application as Vectors for Delivery of Peptide and Protein-Based Cargo Molecules." Pharmaceutics 15, no. 8 (August 7, 2023): 2093. http://dx.doi.org/10.3390/pharmaceutics15082093.

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Peptides and proteins, two important classes of biomacromolecules, play important roles in the biopharmaceuticals field. As compared with traditional drugs based on small molecules, peptide- and protein-based drugs offer several advantages, although most cannot traverse the cell membrane, a natural barrier that prevents biomacromolecules from directly entering cells. However, drug delivery via cell-penetrating peptides (CPPs) is increasingly replacing traditional approaches that mediate biomacromolecular cellular uptake, due to CPPs’ superior safety and efficiency as drug delivery vehicles. In this review, we describe the discovery of CPPs, recent developments in CPP design, and recent advances in CPP applications for enhanced cellular delivery of peptide- and protein-based drugs. First, we discuss the discovery of natural CPPs in snake, bee, and spider venom. Second, we describe several synthetic types of CPPs, such as cyclic CPPs, glycosylated CPPs, and D-form CPPs. Finally, we summarize and discuss cell membrane permeability characteristics and therapeutic applications of different CPPs when used as vehicles to deliver peptides and proteins to cells, as assessed using various preclinical disease models. Ultimately, this review provides an overview of recent advances in CPP development with relevance to applications related to the therapeutic delivery of biomacromolecular drugs to alleviate diverse diseases.
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Ivanov, Yuri D., Vadim Yu Tatur, Alexander V. Glukhov, and Vadim S. Ziborov. "Concentration Sensitivity of Nucleic Acid and Protein Molecule Detection Using Nanowire Biosensors." Biophysica 1, no. 3 (August 14, 2021): 328–33. http://dx.doi.org/10.3390/biophysica1030024.

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The concentration detection limit (DL) of biomacromolecules attainable using a nanowire detector has become a topical issue. A DL of 10−15 M is required to reveal oncological and infectious diseases at an early stage. This study discusses the DL experimentally attainable in the subfemtomolar concentration range, and possible mechanisms explaining such a low-concentration DL through the cooperative effect of biomacromolecular complexes formed on the surface of the nanowire (NW) chip near the nanowire.
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Kaupbayeva, Bibifatima, and Alan J. Russell. "Polymer-enhanced biomacromolecules." Progress in Polymer Science 101 (February 2020): 101194. http://dx.doi.org/10.1016/j.progpolymsci.2019.101194.

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Ruso, Juan M., and Natalia Hassan. "Role of Biomacromolecules in Biomedical Engineering." Current Topics in Medicinal Chemistry 18, no. 14 (October 10, 2018): 1171–87. http://dx.doi.org/10.2174/1568026618666180816155917.

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Biomacromolecules structures and their interaction between different systems have been extensively studied in the last years. Nevertheless, in the medicinal context, it has not been studied deeply. For this reason, the interest to investigate the behavior of different biomacromolecules such us proteins, organelles, phospholipids, etc. with soft materials has opened new research lines. Computational and experimental methodologies have tried to answer different questions that have been difficult to solve, due to the complexity of the phenomenon, as an example, competition between biomacromolecules and soft materials for a specific organ. In this review, we would like to demonstrate how soft materials influence the biomacromolecules structures and how to change their response, biodistribution and also biocompatibility for future applications.
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Ling, Jordy Kim Ung, and Kunn Hadinoto. "Deep Eutectic Solvent as Green Solvent in Extraction of Biological Macromolecules: A Review." International Journal of Molecular Sciences 23, no. 6 (March 21, 2022): 3381. http://dx.doi.org/10.3390/ijms23063381.

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Greater awareness of environmental sustainability has driven many industries to transition from using synthetic organic solvents to greener solvents in their manufacturing. Deep eutectic solvents (DESs) have emerged as a highly promising category of green solvents with well-demonstrated and wide-ranging applications, including their use as a solvent in extraction of small-molecule bioactive compounds for food and pharmaceutical applications. The use of DES as an extraction solvent of biological macromolecules, on the other hand, has not been as extensively studied. Thereby, the feasibility of employing DES for biomacromolecule extraction has not been well elucidated. To bridge this gap, this review provides an overview of DES with an emphasis on its unique physicochemical properties that make it an attractive green solvent (e.g., non-toxicity, biodegradability, ease of preparation, renewable, tailorable properties). Recent advances in DES extraction of three classes of biomacromolecules—i.e., proteins, carbohydrates, and lipids—were discussed and future research needs were identified. The importance of DES’s properties—particularly its viscosity, polarity, molar ratio of DES components, and water addition—on the DES extraction’s performance were discussed. Not unlike the findings from DES extraction of bioactive small molecules, DES extraction of biomacromolecules was concluded to be generally superior to extraction using synthetic organic solvents.
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KANEKO, Yoshiro, and Jun-ichi KADOKAWA. "Biomacromolecules as Organic Resources." NIPPON GOMU KYOKAISHI 81, no. 3 (2008): 112–17. http://dx.doi.org/10.2324/gomu.81.112.

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Zhang, Luyu, Zirong Dong, Wenjuan Liu, Xiying Wu, Haisheng He, Yi Lu, Wei Wu, and Jianping Qi. "Novel Pharmaceutical Strategies for Enhancing Skin Penetration of Biomacromolecules." Pharmaceuticals 15, no. 7 (July 16, 2022): 877. http://dx.doi.org/10.3390/ph15070877.

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Skin delivery of biomacromolecules holds great advantages in the systemic and local treatment of multiple diseases. However, the densely packed stratum corneum and the tight junctions between keratinocytes stand as formidable skin barriers against the penetration of most drug molecules. The large molecular weight, high hydrophilicity, and lability nature of biomacromolecules pose further challenges to their skin penetration. Recently, novel penetration enhancers, nano vesicles, and microneedles have emerged as efficient strategies to deliver biomacromolecules deep into the skin to exert their therapeutic action. This paper reviews the potential application and mechanisms of novel skin delivery strategies with emphasis on the pharmaceutical formulations.
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Ma, Ji, Yu-Min Yin, Hai-Ling Liu, and Meng-Xia Xie. "Interactions of Flavonoids with Biomacromolecules." Current Organic Chemistry 15, no. 15 (August 1, 2011): 2627–40. http://dx.doi.org/10.2174/138527211796367345.

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Dissertations / Theses on the topic "Biomacromolecules"

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Marrington, Rachel. "Polarised spectroscopy of biomacromolecules." Thesis, University of Warwick, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.409802.

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Blom, Hans. "Purification Processes for Complex Biomacromolecules." Doctoral thesis, Uppsala universitet, Fysikalisk-organisk kemi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-172892.

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This thesis details various techniques and considerations for the purification of complex biomacromolecules.   Initially an α-mannosidase from babaco fruit was purified using anion exchange-, lectin affinity- and size exclusion chromatography.  The enzyme was approximately 260-280 kDa in size with an apparent an unusual octagonal stoichiometry and displayed properties similar to other known plant α-mannosidases.   Mucins were fractionated by ion exchange and size exclusion chromatography to assess the properties that govern the mucin surface coating interactions in biomaterial research.  Commercially available mucins, of bovine and porcine origin, as wells as crude human mucin were tested. All showed to consist of a population of molecules which differ in size, charge and composition.   The third part of the thesis concerns different aspects of plasmid DNA purification processes. A two-step method for analysis of plasmid DNA consisting of size exclusion followed by thiophilic adsorption chromatography was evaluated. It allowed determination of the supercoiled plasmid DNA concentration in all process steps without requirement for extensive sample preparation. This method was shown to be fully comparable in terms of accuracy to capillary gel electrophoresis, considered as the industry standard. Purification of plasmid DNA generally involves bacterial cell alkaline lysis, which creates a solution with flocculate material which needs to be removed prior to further processing. The addition of ammonium hydrogen carbonate to the suspension was evaluated to clarify the solution. The released carbon dioxide and ammonium lifts the flocculate to the surface and allows draining of a clear solution. The method is fully scalable, does not affect the plasmid DNA quality and requires no special equipment. Thiophilic adsorption chromatography was evaluated for simplification of an existing commercial large scale purification process and was shown to increase both product purity and yields of several tested plasmids. Also, implementation of this step significantly reduced overall production process time.
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King, Mary Catherine. "Novel conjugation strategies for hybrid biomacromolecules." Thesis, University of Ottawa (Canada), 2003. http://hdl.handle.net/10393/28989.

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The work presented in this thesis describes the development of novel methodology for the preparation of macromolecular conjugates using proteins and dendrimers as scaffolds. This methodology is based on the discovery that chemical modification of proteins can be achieved in vacuo, in the absence of solvents, viz., water. The results obtained represent the first attempts to use this methodology to achieve protein modifications that are otherwise difficult or impossible under aqueous conditions. While the inspiration for this research stemmed from practical objectives, much of the work undertaken developed into a proof of principle, not by design, but due to the fact that there is no precedence or established theoretical base for the in vacuo chemical modification of proteins. Initially, the scope of the project involved the design and development of a novel detoxication construct for an artificial liver consisting of an enzyme coupled to lipophilic poly(propyleneimine) dendrimers as partitioning agents for the clearing of hydrophobic compounds from aqueous solution. While the lipophilic dendrimers proved to be feasible partitioning agents when tested with some drugs in aqueous solution, attempts to attach a model enzyme to the construct by established methods in solution met with limited success. The search for better, more efficient methods of tethering, immobilizing and cross-linking enzymes lead to the investigation of alternative conjugation methods. p-Nitrophenylchloroformate is a common activating reagent used in organic synthesis and has been used to activate chemical modifiers for proteins. However, this reagent has not been used for direct chemical modification of proteins because of its insolubility in water. The results obtained show that this reagent, when used with the in vacuo procedure, can activate and cross-link proteins through chemical modification of protein carboxyl groups. In the course of these studies it was observed that a covalent dimer was present in ribonuclease A heated in the absence of reagent. This observation lead to an investigation which demonstrated that proton transfers between interacting carboxylate and ammonium groups in vacuo results in the formation of amide bonds. Compared to solution methods, the in vacuo methods developed are experimentally simple, and may also be carried out without the use of reactive chemical reagents. Glycation of protein amino groups with reducing monosaccharides can readily be achieved by the formation of stable ketoamine derivatives using the in vacuo methodology. (Abstract shortened by UMI.)
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Zhang, Xiao. "Adsorption of Biomacromolecules onto Polysaccharide Surfaces." Diss., Virginia Tech, 2014. http://hdl.handle.net/10919/52574.

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Plant cell wall polysaccharides are abundant natural polymers making them potential sources for sustainable and biodegradable materials. Interfacial behavior, including adsorption and enzymatic degradation, of several plant cell wall polysaccharides and their derivatives were studied with a quartz crystal microbalance with dissipation monitoring (QCM-D), surface plasmon resonance (SPR) and atomic force microscopy (AFM). Xyloglucan adsorption isotherms were obtained to probe how cellulose-hemicellulose interactions were affected by the type of cellulose substrate and molar mass of xyloglucan. Xyloglucan as small as a heptasaccharide still adsorbed irreversibly onto cellulose. Carboxymethyl cellulose (CMC) adsorption onto cellulose and viscoelastic properties and water contents of the adsorbed CMC layers were obtained from a combination of QCM-D and SPR data. The CMC samples formed hydrated and viscoelastic layers compared to the relatively rigid xyloglucan layer. Pectin model surfaces were prepared by pectin adsorption from citric phosphate buffer onto gold substrates. These pectin model surfaces were used for subsequent interaction studies with xyloglucan and enzymatic degradation behavior. There is a strong correlation between the degree of esterification (DE) and film resistance to degradation with the high DE being the most susceptible to degradation. The adsorption of two mixed linkage glucans (MLG), barley and lichen MLG, onto regenerated cellulose (RC) surfaces in the absence and presence of other matrix polysaccharides was studied. Viscoelastic properties of the resulting layer were compared as a function of the proprotion of '-(1''3) linkages with lichen MLG forming softer gel-like layers on RC. The lichen MLG layers were further used for enzymatic degradation studies with respect to enzyme concentration, temperature, pH and ionic strength. These studies show that polymer adsorption is a promising strategy to modify material surfaces and provides fundamental understanding of interactions and biodegradation of cell wall polysaccharides at solid/liquid interfaces.
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Ustriyana, Putu Ayu Ditta Sarita. "Natural and Synthetic Biomacromolecules in Biomineralization." University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1573830824042347.

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Luginbühl, Reto. "Photobonding of biomacromolecules to Silicon Nitride surfaces /." [S.l.] : [s.n.], 1997. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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Su, Shunxing Pelton Robert H. "Biomacromolecules in paper for strength and bio-detection." *McMaster only, 2007.

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Shen, Shengyi. "Development of Split-protein Systems for Interrogating Biomacromolecules." Diss., The University of Arizona, 2013. http://hdl.handle.net/10150/308885.

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The specific interactions of macromolecules along with the activity of enzymes are central to all aspects of biology. It is well recognized that when the relative concentration or activity of macromolecules is perturbed, it can lead to human diseases. Thus, the development of simple methods for the detection of macromolecules and the activity of enzymes in complex environments is important for understanding biology. Moreover, the development of methods for measuring interactions allows for the testing of inhibitors that can be used as tools or drugs for improving human health. Towards this goal, a promising new method has been developed, which is the focus of this thesis, called split-protein reassembly or protein fragment complementation. In this method, a protein reporter, such as the green fluorescent protein or firefly luciferase, is dissected into two fragments, which are attached to designed adaptor proteins. The designed split-protein systems only produce a measurable signal, either fluorescence or luminescence, when a specific macromolecular interaction or activity is present. In this thesis, I have extended previous research on the direct detection of DNA using split-protein sensors utilizing a red fluorescent protein, dsRED from Discosoma that allows for multiplexed DNA detection. I have designed a new split-luciferase based sensor for detection of poly (ADP-ribose) or PAR, which plays a key role in the response to DNA damage and have applied it for monitoring the activity of poly (ADP-ribose) glycohydrolase that controls PAR levels in the cell. Furthermore, I have significantly expanded upon a three-hybrid split-luciferase system for identifying protein kinase inhibitors. I have designed and tested two orthogonal peptide based chemical inducers of dimerization based on BAD and p53mt conjugates. I have studied these chemically induced dimerization systems in detail in order to begin to provide a theoretical basis for the observed experimental results. Finally, in a less related area, I have developed methods for producing water soluble semiconductor nanoparticles called Quantum Dots (QDs), with potential application in biological imaging. I have developed methods for functionalizing the QDs with orthogonal peptides, which can be potentially used for the assembly of high affinity non-covalent QD targeted proteins.
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Zhao, Chao. "Molecular Understanding of the Interaction of Biomacromolecules with Polymers." University of Akron / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=akron1373489167.

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Wang, Chao. "Renewable Natural Polymer Thin Films and Their Interactions with Biomacromolecules." Diss., Virginia Tech, 2014. http://hdl.handle.net/10919/64909.

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Natural polymers from renewable resources have attracted increasing interest as candidates for renewable energy and functional materials. In this work, the interactions between natural polymer thin films and biomacromolecules were studied via surface analysis techniques, such as a quartz crystal microbalance with dissipation monitoring (QCM-D), surface plasmon resonance (SPR) and atomic force microscopy (AFM). Chitinase activity on regenerated chitin (RChitin) films was studied by QCM-D and AFM. The optimal temperature and pH for chitinase activity on surfaces determined by QCM-D and AFM were consistent with bulk solution studies in the literature. Results from QCM-D also indicated that chitinase showed higher activity on fully acetylated chitin than highly deacetylated chitosan. Nanocrystalline chitin (Chitin NC) thin films were prepared by spincoating a nanocrystalline chitin colloidal suspension onto solid surfaces. Solvent exchange experiments via QCM-D with H2O/D2O revealed that Chitin NC films had more water than RChitin films of similar thickness. Results from QCM-D demonstrated that Chitin NC films had high bovine serum albumin loading capacity, and chitinase not only degraded, but also caused swelling of the chitin nanocrystals. Adsorption of human serum albumin (HSA) and fibrinogen (HFN) onto bare gold, regenerated cellulose (RC) and RChitin thin films was studied by SPR and QCM-D. Studies by SPR indicated that HSA and HFN formed close-packed monolayers on gold surfaces and sub-monolayers on polysaccharide surfaces, and the adsorption affinity of HSA for polysaccharide surfaces was greater than that of HFN. Results from QCM-D and SPR showed that the protein layers on polysaccharide surfaces had more associated water than proteins on gold surfaces. The dehydrogenative polymerization of monolignols catalyzed by physically immobilized horseradish peroxidase was investigated using QCM-D and AFM. Results from QCM-D and AFM showed that coniferyl and p-coumaryl alcohol underwent polymerization directly, whereas sinapyl alcohol required the addition of a nucleophile for polymerization. Studies by QCM-D and AFM also indicated that the surface-initiated polymerization was greatly affected by the support surface, monolignol concentration, hydrogen peroxide concentration and temperature. Thin films of dehydrogenative polymer (DHP), kraft (KL), organosolv (OL) and milled wood (MWL) lignins were used to study the enzymatic degradation of lignin mediated by lignin peroxidase (LiP) and manganese peroxidase (MnP). Results from QCM-D showed that the initial rates for degradation catalyzed by LiP increased in the order: KL < OL < MWL < guaiacyl DHP (G-DHP) < p-hydroxyphenyl DHP (H-DHP). In contrast, manganese peroxidase only degraded DHP films with a faster initial rate for G-DHP than H-DHP. Adsorption of hemicelluloses onto KL, OL and MWL thin films was studied by QCM-D and SPR. Results from QCM-D showed that hemicelluloses with different structures displayed very different adsorption behavior. Adsorption isotherms from QCM-D and SPR indicated that xyloglucan possessed stronger affinity for KL and OL films than MWL films. Data from QCM-D and SPR revealed that xyloglucan formed less hydrated layers on lignin surfaces compared to RC surfaces, and the adsorbed xyloglucan layers on different lignin films had similar percentages of coupled water.
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Books on the topic "Biomacromolecules"

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Tsai, C. Stan. Biomacromolecules. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470080124.

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Tsai, C. Stan. Biomacromolecules. New York: John Wiley & Sons, Ltd., 2006.

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Lenaz, Giorgio, and Giulio Milazzo, eds. Bioelectrochemistry of Biomacromolecules. Basel: Birkhäuser Basel, 1996. http://dx.doi.org/10.1007/978-3-0348-9179-0.

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Pharmaceutical chemistry: Therapeutic aspects of biomacromolecules. Chichester: Wiley, 2002.

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Y, Aboul-Enein Hassan, ed. Analytical and preparative separation methods of biomacromolecules. New York: Marcel Dekker, 1999.

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Messerschmidt, Albrecht. X-ray crystallography of biomacromolecules: A practical guide. Weinheim: Wiley-VCH, 2007.

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Kapoor, Deepak N. Biocompatible nanomaterials for targeted and controlled delivery of biomacromolecules. New York,NY: ASME Press/Momentum Press, 2013.

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D, Varfolomeyev S., and Zaikov Gennadiĭ Efremovich, eds. Molecular polymorphism of man: Structural and functional individual multiformity of biomacromolecules. Hauppauge, NY: Nova Science Publishers, 2009.

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D, Varfolomeyev S., and Zaikov Gennadiĭ Efremovich, eds. Molecular polymorphism of man: Structural and functional individual multiformity of biomacromolecules. Hauppauge, NY: Nova Science Publishers, 2009.

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Hanford Symposium on Health and the Environment (34th 1995 Pasco, Wash.). Biomacromolecules--from 3-D to applications: Thirty-fourth Hanford Symposium on Health and the Environment, October 23-26, 1995, Pasco, Washington, U.S.A. Columbus, OH: Battelle Press, 1997.

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Book chapters on the topic "Biomacromolecules"

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Brabec, Viktor, Vladimír Vetterl, and Oldřich Vrána. "Electroanalysis of biomacromolecules." In Experimental Techniques in Bioelectrochemistry, 287–359. Basel: Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-7607-0_5.

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Rathi, Prakash C., Christopher Pfleger, Simone Fulle, Doris L. Klein, and Holger Gohlke. "Statics of Biomacromolecules." In Modeling of Molecular Properties, 281–99. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527636402.ch18.

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Brabec, Viktor, Vladimír Kleinwächter, and Vladimír Vetterl. "Structure, chemical reactivity and electromagnetic properties of nucleic acids." In Bioelectrochemistry of Biomacromolecules, 1–104. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_1.

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Urry, Dan W., and Chi-Hao Luan. "Proteins: Structure, folding and function." In Bioelectrochemistry of Biomacromolecules, 105–82. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_2.

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Hill, H. Allen O., C. Bruce Moore, and David M. A. NabiRahni. "Electrochemistry of redox proteins." In Bioelectrochemistry of Biomacromolecules, 183–204. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_3.

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Armstrong, Fraser A. "Applications of voltammetric methods for probing the chemistry of redox proteins." In Bioelectrochemistry of Biomacromolecules, 205–55. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_4.

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Gilbert, Hiram F. "Thiol/disulfide exchange and redox potentials of proteins." In Bioelectrochemistry of Biomacromolecules, 256–324. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_5.

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Feinberg, Benjamin A., and Michael D. Ryan. "Electrochemistry of iron-sulfur proteins." In Bioelectrochemistry of Biomacromolecules, 325–59. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_6.

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Pye, David A. "Glycosaminoglycans: Sulphated polysaccharides of the cell surface and extracellular matrix." In Bioelectrochemistry of Biomacromolecules, 360–84. Basel: Birkhäuser Basel, 1997. http://dx.doi.org/10.1007/978-3-0348-9179-0_7.

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Li, Qing, Zackary N. Scholl, and Piotr E. Marszalek. "Nanomechanics of Single Biomacromolecules." In Handbook of Nanomaterials Properties, 1077–123. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-31107-9_13.

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Conference papers on the topic "Biomacromolecules"

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Biczysko, Malgorzata, Pavel Afonine, Mark Waller, Holger Kruse, Nigel Moriarty, and Yanting Xu. "Q | R: QUANTUM-BASED REFINEMENT OF BIOMACROMOLECULES." In 2022 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2022. http://dx.doi.org/10.15278/isms.2022.mi01.

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MONDAINI, R. P., and S. P. VILELA. "A PROPOSAL FOR MODELLING THE STRUCTURE OF BIOMACROMOLECULES." In BIOMAT 2010 - International Symposium on Mathematical and Computational Biology. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814343435_0005.

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Laptinskiy, Kirill A., Sergey A. Burikov, Maria Y. Khmeleva, and Tatiana A. Dolenko. "Laser spectroscopy of interactions of carbon nanoparticles with biomacromolecules." In XV International Conference on Pulsed Lasers and Laser Applications, edited by Victor F. Tarasenko, Anton V. Klimkin, and Maxim V. Trigub. SPIE, 2021. http://dx.doi.org/10.1117/12.2608152.

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Davydova, N. K., O. V. Sinitsyna, and K. E. Zinoviev. "Preparation of synthetic copolymers potentially capable to interact with biomacromolecules." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738449.

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Glukhova, Olga E., Elena L. Kossovich, Anna S. Kolesnikova, and Liyana R. Menisheva. "Molecular dynamics study of phospholipid biomacromolecules using a coarse-grained model." In SPIE BiOS, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2013. http://dx.doi.org/10.1117/12.2003176.

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Hobza, Pavel, George Maroulis, and Theodore E. Simos. "Calculations of the Stabilization Energies of the Building Blocks of Biomacromolecules." In Computational Methods in Science and Engineering. AIP, 2007. http://dx.doi.org/10.1063/1.2827024.

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Waye, Mary Miu Yee, Carmen Wing Han Chan, and Ruquan Ye. "Graphene: A New Material for Wound Healing." In International Electronic Conference on Biomolecules: Biomacromolecules and the Modern World Challenges. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/iecbm2022-13693.

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Johannessen, Christian, Robert Pendrill, Lutz Hecht, Göran Widmalm, Laurence D. Barron, P. M. Champion, and L. D. Ziegler. "Raman Optical Activity of Biomacromolecules: Structural Analysis of Sugar Moieties in Glycoproteins." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482288.

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Vervald, Ekaterina, Alexey Vervald, Kirill A. Laptinskiy, and Tatiana Dolenko. "Fluorescent properties of nanodiamonds in result of interactions of nanodiamonds with biomacromolecules in water." In Biophotonics: Photonic Solutions for Better Health Care, edited by Jürgen Popp, Valery V. Tuchin, and Francesco S. Pavone. SPIE, 2018. http://dx.doi.org/10.1117/12.2306592.

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Krasova, Yu V., O. V. Tkachenko, E. N. Sigida, N. V. Evseeva, G. L. Burygin, and Y. V. Lobachev. "Features of the development of wheat tissue culture during processing bacterial biomacromolecules and cells." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-236.

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Reports on the topic "Biomacromolecules"

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Cosman, M., V. V. Krishnan, and R. Maxwell. Development of Nuclear Magnetic Resonance Pulse Sequences and Probes to Study Biomacromolecules. Office of Scientific and Technical Information (OSTI), February 2001. http://dx.doi.org/10.2172/15005390.

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Jones, Robert M., Alison K. Thurston, Robyn A. Barbato, and Eftihia V. Barnes. Evaluating the Conductive Properties of Melanin-Producing Fungus, Curvularia lunata, after Copper Doping. Engineer Research and Development Center (U.S.), November 2020. http://dx.doi.org/10.21079/11681/38641.

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Abstract:
Melanins are pigmented biomacromolecules found throughout all domains of life. Of melanins’ many unique properties, their malleable electrically conductive properties and their ability to chelate could allow them to serve as material for bioelectronics. Studies have shown that sheets or pellets of melanin conduct low levels of electricity; however, electrical conductance of melanin within a cellular context has not been thoroughly investigated. In addition, given the chelating properties of melanin, it is possible that introducing traditionally con-ductive metal ions could improve the conductivity. Therefore, this study investigated the conductive properties of melanized cells and how metal ions change these. We measured the con-ductivity of pulverized Curvularia lunata, a melanized filamentous fungi, with and without the addition of copper ions. We then com-pared the conductivity measurements of the fungus to chemically synthesized, commercially bought melanin. Our data showed that the conductivity of the melanized fungal biomass was an order of magnitude higher when grown in the presence of copper. However, it was two orders of magnitude less than that of synthetic melanin. Interestingly, conductance was measurable despite additional constituents in the pellet that may inhibit conductivity. Therefore, these data show promising results for using melanized cells to carry electrical signals.
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