Relevant bibliographies by topics / Proteins cross-link

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Proteins cross-link'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Proteins cross-link"

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Bode, Tom, Kai Höltje, Sara Leal-Marin, Marc Müller, and Birgit Glasmacher. "Evaluation and Implementation of Biocompatible Methods for the Cross-linking of Plasma Proteins." Current Directions in Biomedical Engineering 7, no. 2 (2021): 187–90. http://dx.doi.org/10.1515/cdbme-2021-2048.

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Abstract Autologous plasma proteins can be used to fabricate patient specific cardiovascular implants but need to be cross-linked to increase their mechanical strength and reduce water solubility. Glutaraldehyde is the state-of-the-art solution but its reaction products have been shown to be cytotoxic and pro-inflammatory. In this work, it has been shown, that cross-linking of plasma proteins with biocompatible alternatives to glutaraldehyde is possible. This was achieved by identifying four candidate substances (thrombin, transglutaminase, genipin, EDC) from current literature and investigati
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Fife, R. S., B. Caterson, and S. L. Myers. "Identification of link proteins in canine synovial cell cultures and canine articular cartilage." Journal of Cell Biology 100, no. 4 (1985): 1050–55. http://dx.doi.org/10.1083/jcb.100.4.1050.

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Link proteins are glycoproteins in cartilage that are involved in the stabilization of aggregates of proteoglycans and hyaluronic acid. We have identified link proteins in synovial cell cultures form normal canine synovium using sodium dodecyl sulfate-polyacrylamide gel electrophoresis, immunofluorescence, and immunolocation with specific antibodies by electrophoretic transfer. We have also found evidence for the synthesis of link proteins in these cultures by fluorography of radiolabeled synovial cell extracts. We have identified a 70,000 mol-wt protein in canine synovial cell culture extract
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Migliorini, Elisa, Dhruv Thakar, Jens Kühnle, et al. "Cytokines and growth factors cross-link heparan sulfate." Open Biology 5, no. 8 (2015): 150046. http://dx.doi.org/10.1098/rsob.150046.

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The glycosaminoglycan heparan sulfate (HS), present at the surface of most cells and ubiquitous in extracellular matrix, binds many soluble extracellular signalling molecules such as chemokines and growth factors, and regulates their transport and effector functions. It is, however, unknown whether upon binding HS these proteins can affect the long-range structure of HS. To test this idea, we interrogated a supramolecular model system, in which HS chains grafted to streptavidin-functionalized oligoethylene glycol monolayers or supported lipid bilayers mimic the HS-rich pericellular or extracel
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Zhang, Pan, Deepa Sridharan, Michael Acosta та Muriel Lambert. "FANCD2 Localizes to Cross-Linked Induced Nuclear Foci That Are Distinct From Those to Which αaII Spectrin and the Cross-Link Repair Protein, XPF, Co-Localize, Indicating An Involvement of These Proteins in Different Steps of the DNA Interstrand Cross-Link Repair Process." Blood 114, № 22 (2009): 3196. http://dx.doi.org/10.1182/blood.v114.22.3196.3196.

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Abstract Abstract 3196 Poster Board III-133 The hereditary bone marrow failure disorder, Fanconi anemia (FA), is characterized by a markedly increased incidence of acute myelogenous leukemia, diverse congenital abnormalities and a defect in ability to repair DNA interstrand cross-links. We have previously shown that in FA cells there is a deficiency in the structural protein nonerythroid a spectrin (aSpII), which is involved in repair of DNA interstrand cross-links and binds to cross-linked DNA. aSpII co-localizes in nuclear foci with FANCA and the cross-link repair protein, XPF, after normal
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Staknis, D., and R. Reed. "Direct interactions between pre-mRNA and six U2 small nuclear ribonucleoproteins during spliceosome assembly." Molecular and Cellular Biology 14, no. 5 (1994): 2994–3005. http://dx.doi.org/10.1128/mcb.14.5.2994-3005.1994.

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Highly purified mammalian spliceosomal complex B contains more than 30 specific protein components. We have carried out UV cross-linking studies to determine which of these components directly contacts pre-mRNA in purified prespliceosomal and spliceosomal complexes. We show that heterogeneous nuclear ribonucleoproteins cross-link in the nonspecific complex H but not in the B complex. U2AF65, which binds to the 3' splice site, is the only splicing factor that cross-links in purified prespliceosomal complex E. U2AF65 and the U1 small nuclear ribonucleoprotein particle (snRNP) are subsequently de
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Staknis, D., and R. Reed. "Direct interactions between pre-mRNA and six U2 small nuclear ribonucleoproteins during spliceosome assembly." Molecular and Cellular Biology 14, no. 5 (1994): 2994–3005. http://dx.doi.org/10.1128/mcb.14.5.2994.

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Highly purified mammalian spliceosomal complex B contains more than 30 specific protein components. We have carried out UV cross-linking studies to determine which of these components directly contacts pre-mRNA in purified prespliceosomal and spliceosomal complexes. We show that heterogeneous nuclear ribonucleoproteins cross-link in the nonspecific complex H but not in the B complex. U2AF65, which binds to the 3' splice site, is the only splicing factor that cross-links in purified prespliceosomal complex E. U2AF65 and the U1 small nuclear ribonucleoprotein particle (snRNP) are subsequently de
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ALI, Sohail T., John R. COGGINS, and Howard T. JACOBS. "The study of cell-death proteins in the outer mitochondrial membrane by chemical cross-linking." Biochemical Journal 325, no. 2 (1997): 321–24. http://dx.doi.org/10.1042/bj3250321.

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Chemical cross-linking was used to study the interactions of the anti-cell-death protein Bcl2 with other proteins in the outer mitochondrial membrane. Cross-linking of mitochondrial surface proteins produced a large Bcl2-containing complex (> 200 kDa), and a Bcl2-derived peptide was shown to cross-link specifically with a mitochondrial protein identified by immunoblotting as Raf-1 kinase.
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Kaddar, Tagrid, and Madeleine Carreau. "Fanconi Anemia Proteins and Their Interacting Partners: A Molecular Puzzle." Anemia 2012 (2012): 1–11. http://dx.doi.org/10.1155/2012/425814.

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In recent years, Fanconi anemia (FA) has been the subject of intense investigations, primarily in the DNA repair research field. Many discoveries have led to the notion of a canonical pathway, termed the FA pathway, where all FA proteins function sequentially in different protein complexes to repair DNA cross-link damages. Although a detailed architecture of this DNA cross-link repair pathway is emerging, the question of how a defective DNA cross-link repair process translates into the disease phenotype is unresolved. Other areas of research including oxidative metabolism, cell cycle progressi
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Neubacher, Saskia, Jordy M. Saya, Alessia Amore, and Tom N. Grossmann. "In Situ Cyclization of Proteins (INCYPRO): Cross-Link Derivatization Modulates Protein Stability." Journal of Organic Chemistry 85, no. 3 (2019): 1476–83. http://dx.doi.org/10.1021/acs.joc.9b02490.

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Figueroa-Espinoza, M. C., M. H. Morel, A. Surget, et al. "Attempt to cross-link feruloylated arabinoxylans and proteins with a fungal laccase." Food Hydrocolloids 13, no. 1 (1999): 65–71. http://dx.doi.org/10.1016/s0268-005x(98)00072-1.

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Dissertations / Theses on the topic "Proteins cross-link"

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Villas, Boas Mariana Battaglin 1981. "Efeito da polimerização por transglutaminase e da proteólise na estrutura e antigenicidade da 'Beta'-lactoglobulina." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/256380.

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Orientador: Flavia Maria Netto<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos<br>Made available in DSpace on 2018-08-20T14:16:39Z (GMT). No. of bitstreams: 1 VillasBoas_MarianaBattaglin_D.pdf: 3357506 bytes, checksum: 10d878e81440a9db2f379bd1dd93146f (MD5) Previous issue date: 2012<br>Resumo: Tratamento térmico, alta pressão ou hidrólise enzimática, utilizados em conjunto ou separadamente, podem alterar determinantes antigênicos (epítopos) presentes nas proteínas, e têm sido estudados como estratégia para obtenção de produtos com menor potencial
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Drew, Gail L. "DNA-Protein Cross-Linking by Pyrrolizidine Alkaloids." DigitalCommons@USU, 1997. https://digitalcommons.usu.edu/etd/3919.

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Pyrrolizidine alkaloids (PAs) are natural plant compounds found in hundreds of plant species worldwide and are reported to have cytotoxic, carcinogenic, antimitotic, and gentotoxic activity. PAs are metabolized by the cytochrome P450 (CYP) sytem to the pyrrole or the N-oxide form. They pyrroles are bifunctional electrophillic alkylators that bind cellular nucleophiles such as DNA and proteins and disrupt normal cell processes, including DNA replication and gene transcription, and can cause megalocytosis. The pyrroles dehyrosenecionine (DHSN) and dehydromoncrotaline (DHMO) are among the most po
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Book chapters on the topic "Proteins cross-link"

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Tripathi, Priyanka, Zhihui Zhu, Haiyan Qin, et al. "Cross-Link/Proximity Ligation Assay for Visualization of Lipid and Protein Complexes in Lipid Rafts." In Methods in Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0814-2_20.

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Cavalli, Giacomo, Valerio Orlando,, and Renato Paro. "Mapping DNA target sites of chromatin-associated proteins by formaldehyde cross-linking in Drosophila embryos." In Chromosome Structural Analysis. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780199636990.003.0002.

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Abstract The method described here allows the mapping of protein-DNA interactions through the ability of formaldehyde to cross-link proteins and nucleic acids in living cells. Formaldehyde is a very reactive dipolar compound which reacts with the amino groups of proteins and amino acids (1, 2). It shows no reactivity, however, towards free double-stranded DNA, and thus does not cause the extensive DNA damage seen after prolonged exposure to other crosslinking reagents such as UV. Each formaldehyde molecule has the capacity to interact with two amino groups. Therefore DNA-protein, protein-prote
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Kerr, David J., Daniel Haller, and Jaap Verweij. "Principles of chemotherapy." In Oxford Textbook of Cancer Biology, edited by Francesco Pezzella, Mahvash Tavassoli, and David J. Kerr. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780198779452.003.0028.

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Systemic cancer treatment stems initially from empirically discovered DNA synthesis inhibitors, which either deplete the cell of nucleotides, induce cross-link, or cause DNA single and double strand breaks or impair the cellular machinery of DNA repair, using mechanistically diverse drugs. A period of enlightenment followed, with anticancer drug development driven by an increased understanding of enzymes and pathways involved in cell signalling, control of angiogenesis, and epigenetics. This provided a parallel path towards precision cancer medicine where specific drugs can be targeted to pati
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Ide, Hiroshi, Toshiaki Nakano, Mahmoud I. Shoulkamy, and Amir M. H. Salem. "Formation, Repair, and Biological Effects of DNA–Protein Cross-Link Damage." In Advances in DNA Repair. InTech, 2015. http://dx.doi.org/10.5772/59683.

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Morse, Julia C. "Cross-Border Banking in a Globalized Era." In The Bankers' Blacklist. Cornell University Press, 2022. http://dx.doi.org/10.7591/cornell/9781501761515.003.0001.

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This introductory chapter provides an overview of the link between cross-border banking and domestic policy. Every country in the world relies on bank-to-bank networks for some type of commerce, and it is this near-universal dependence that makes it a uniquely powerful tool of pressure. Countries may be able to forgo foreign investment or sell bonds to domestic markets, but governments cannot afford to be cut off from the global banking community. For this reason, bank networks and operating practices can have profound effects on the domestic policies of states. The chapter describes the Finan
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Thiede, Bernd, and Brigitte Wittmann-Liebold. "[29] Analysis of RNA-protein cross-link sites by matrix-assisted laser desorption/ionization mass spectrometry and N-terminal microsequencing." In Methods in Enzymology. Elsevier, 2000. http://dx.doi.org/10.1016/s0076-6879(00)18068-1.

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Sawle, P. J., and F. M. Pope. "Connective Tissue Disorders – Ehlers–Danlos Syndrome." In Genomics and Clinical Diagnostics. The Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781782628217-00376.

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Ehlers–Danlos Syndrome (EDS) is a group of connective tissue disorders which are both heterogeneous and heritable. The condition is a result of collagen defects, which include genetic variations and collagen protein processing. Collagen is present in fibrous tissues, such as skin, tendons and ligaments, and is also found in cartilage, blood vessels, the cornea, bones and the gut, highlighting its importance and explaining the varied pathophysiology of collagen conditions. These disorders were classified into six major types based upon the genetic and diagnostic variability and pathophysiology
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Conference papers on the topic "Proteins cross-link"

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Daďová, Jitka, Petr Orság, Radek Pohl, Marie Brázdová, Miroslav Fojta, and Michal Hocek. "Study of DNA-protein interactions by cross-link formation using aqueous Michael addition." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414240.

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Adeniran, Oluwaseyefunmi, and Sechene S. Gololo. "In vitroantiglycation and protein cross-link breakage effects ofMurraya koenigiileaf extracts and their phytochemical composition." In ASPET 2023 Annual Meeting Abstracts. American Society for Pharmacology and Experimental Therapeutics, 2023. http://dx.doi.org/10.1124/jpet.122.286220.

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