Bibliografías temáticas / Protease

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Literatura académica sobre el tema "Protease"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 9 de junio de 2025

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Artículos de revistas sobre el tema "Protease"

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Watanabe, Katsuji, and Koichi Hayano. "Source of soil protease in paddy fields." Canadian Journal of Microbiology 39, no. 11 (November 1, 1993): 1035–40. http://dx.doi.org/10.1139/m93-157.

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Properties of soil proteases and proteases from Bacillus spp. obtained from water-logged paddy fields treated with organic manure or chemical fertilizer or not treated with fertilizer were compared to elucidate the sources of soil proteases. The major extractable soil proteases were metal chelator sensitive neutral proteases that were active in hydrolyzing benzyloxycarbonyl-L-phenylalanyl-L-leucine and benzyloxycarbonyl-L-phenylalanyl-L-tyrosyl-L-leucine. In this respect they resembled extracellular proteases from Bacillus subtilis (six isolates), Bacillus cereus (four isolates), and Bacillus
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Mallia-Milanes, Brendan, Antoine Dufour, Christopher Philp, Nestor Solis, Theo Klein, Marlies Fischer, Charlotte E. Bolton, Steven Shapiro, Christopher M. Overall, and Simon R. Johnson. "TAILS proteomics reveals dynamic changes in airway proteolysis controlling protease activity and innate immunity during COPD exacerbations." American Journal of Physiology-Lung Cellular and Molecular Physiology 315, no. 6 (December 1, 2018): L1003—L1014. http://dx.doi.org/10.1152/ajplung.00175.2018.

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Dysregulated protease activity is thought to cause parenchymal and airway damage in chronic obstructive pulmonary disease (COPD). Multiple proteases have been implicated in COPD, and identifying their substrates may reveal new disease mechanisms and treatments. However, as proteases interact with many substrates that may be protease inhibitors or proteases themselves, these webs of protease interactions make the wider consequences of therapeutically targeting proteases difficult to predict. We therefore used a systems approach to determine protease substrates and protease activity in COPD airw
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Paulin, John P., and Francisco C. Franco. "Modified bis‐tetrahydrofuran inhibitors toward improved binding to HIV‐1 proteases." Vietnam Journal of Chemistry 59, no. 5 (October 2021): 563–79. http://dx.doi.org/10.1002/vjch.202000179.

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AbstractHIV treatment includes inhibiting HIV‐1 protease which is responsible for viral maturation. However, HIV‐1 protease responds to drug treatment by mutation making the protease‐resistant to inhibitors. In this study, binding interactions between bis‐tetrahydrofuran‐derived (bis‐THF) inhibitors and HIV‐1 protease were described by molecular docking. We characterized the binding energies and all the amino acids present during the binding of the bis‐THF derivatives to the wild type HIV‐1 protease and several mutant HIV‐1 proteases. We found that the modifications to the structure of darunav
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Kostallas, George, and Patrik Samuelson. "Novel Fluorescence-Assisted Whole-Cell Assay for Engineering and Characterization of Proteases and Their Substrates." Applied and Environmental Microbiology 76, no. 22 (September 17, 2010): 7500–7508. http://dx.doi.org/10.1128/aem.01558-10.

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ABSTRACT We have developed a sensitive and highly efficient whole-cell methodology for quantitative analysis and screening of protease activity in vivo. The method is based on the ability of a genetically encoded protease to rescue a coexpressed short-lived fluorescent substrate reporter from cytoplasmic degradation and thereby confer increased whole-cell fluorescence in proportion to the protease's apparent activity in the Escherichia coli cytoplasm. We demonstrated that this system can reveal differences in the efficiency with which tobacco etch virus (TEV) protease processes different subst
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Hudig, D., N. J. Allison, T. M. Pickett, U. Winkler, C. M. Kam, and J. C. Powers. "The function of lymphocyte proteases. Inhibition and restoration of granule-mediated lysis with isocoumarin serine protease inhibitors." Journal of Immunology 147, no. 4 (August 15, 1991): 1360–68. http://dx.doi.org/10.4049/jimmunol.147.4.1360.

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Abstract To kill other cells, lymphocytes can exocytose granules that contain serine proteases and pore-forming proteins (perforins). We report that mechanism-based isocoumarin inhibitors inhibited the proteases and inactivated lysis. When inhibited proteases were restored, lysis was also restored, indicating that the proteases were essential for lysis. We found three new lymphocyte protease activities, "Asp-ase,"Met-ase," and "Ser-ase," which in addition to ly-tryptase and ly-chymase, comprise five different protease activities in rat RNK-16 granules. The general serine protease inhibitor 3,4
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Taggart, Clifford, Marcus A. Mall, Gilles Lalmanach, Didier Cataldo, Andreas Ludwig, Sabina Janciauskiene, Nicole Heath, et al. "Protean proteases: at the cutting edge of lung diseases." European Respiratory Journal 49, no. 2 (February 2017): 1501200. http://dx.doi.org/10.1183/13993003.01200-2015.

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Proteases were traditionally viewed as mere protein-degrading enzymes with a very restricted spectrum of substrates. A major expansion in protease research has uncovered a variety of novel substrates, and it is now evident that proteases are critical pleiotropic actors orchestrating pathophysiological processes. Recent findings evidenced that the net proteolytic activity also relies upon interconnections between different protease and protease inhibitor families in the protease web.In this review, we provide an overview of these novel concepts with a particular focus on pulmonary pathophysiolo
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Schuhmann, Holger, Ulrike Mogg, and Iwona Adamska. "A new principle of oligomerization of plant DEG7 protease based on interactions of degenerated protease domains." Biochemical Journal 435, no. 1 (March 15, 2011): 167–74. http://dx.doi.org/10.1042/bj20101613.

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Deg/HtrA proteases are a large group of ATP-independent serine endoproteases found in almost every organism. Their usual domain arrangement comprises a trypsin-type protease domain and one or more PDZ domains. All Deg/HtrA proteases form homo-oligomers with trimers as the basic unit, where the active protease domain mediates the interaction between individual monomers. Among the members of the Deg/HtrA protease family, the plant protease DEG7 is unique since it contains two protease domains (one active and one degenerated) and four PDZ domains. In the present study, we investigated the oligome
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Mann, Krin, and Hélène Sanfaçon. "Expanding Repertoire of Plant Positive-Strand RNA Virus Proteases." Viruses 11, no. 1 (January 15, 2019): 66. http://dx.doi.org/10.3390/v11010066.

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Many plant viruses express their proteins through a polyprotein strategy, requiring the acquisition of protease domains to regulate the release of functional mature proteins and/or intermediate polyproteins. Positive-strand RNA viruses constitute the vast majority of plant viruses and they are diverse in their genomic organization and protein expression strategies. Until recently, proteases encoded by positive-strand RNA viruses were described as belonging to two categories: (1) chymotrypsin-like cysteine and serine proteases and (2) papain-like cysteine protease. However, the functional chara
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Karlsson, Anna, Patricia Saravia-Otten, Karin Tegmark, Eva Morfeldt, and Staffan Arvidson. "Decreased Amounts of Cell Wall-Associated Protein A and Fibronectin-Binding Proteins in Staphylococcus aureus sarA Mutants due to Up-Regulation of Extracellular Proteases." Infection and Immunity 69, no. 8 (August 1, 2001): 4742–48. http://dx.doi.org/10.1128/iai.69.8.4742-4748.2001.

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ABSTRACT Data have been presented indicating that Staphylococcus aureus cell surface protein can be degraded by extracellular proteases produced by the same bacterium. We have found that insarA mutant cells, which produce high amounts of four major extracellular proteases (staphylococcal serine protease [V8 protease] [SspA], cysteine protease [SspB], aureolysin [metalloprotease] [Aur], and staphopain [Scp]), the levels of cell-bound fibronectin-binding proteins (FnBPs) and protein A were very low compared to those of wild-type cells, in spite of unaltered or increased transcription of the corr
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Greenfield, Lucy M., Paul W. Hill, Eric Paterson, Elizabeth M. Baggs, and Davey L. Jones. "Do plants use root-derived proteases to promote the uptake of soil organic nitrogen?" Plant and Soil 456, no. 1-2 (September 23, 2020): 355–67. http://dx.doi.org/10.1007/s11104-020-04719-6.

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Abstract Aims The capacity of plant roots to directly acquire organic nitrogen (N) in the form of oligopeptides and amino acids from soil is well established. However, plants have poor access to protein, the central reservoir of soil organic N. Our question is: do plants actively secrete proteases to enhance the breakdown of soil protein or are they functionally reliant on soil microorganisms to undertake this role? Methods Growing maize and wheat under sterile hydroponic conditions with and without inorganic N, we measured protease activity on the root surface (root-bound proteases) or exogen
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Tesis sobre el tema "Protease"

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Wartchow, Charles Aaron. "Carbohydrate protease conjugates (CPC) : stabilized proteases for peptide synthesis /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487847309050511.

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De, Veer Simon J. "Development of novel protease inhibitors for epidermal kallikrein proteases." Thesis, Queensland University of Technology, 2014. https://eprints.qut.edu.au/114508/1/Simon_de%20Veer_Thesis.pdf.

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Preserving the integrity of the skin's outermost layer (the epidermis) is vital for humans to thrive in hostile surroundings. Covering the entire body, the epidermis forms a thin but impenetrable cellular cordon that repels external assaults and blocks the escape of water and electrolytes from within. This structure exists in a perpetual state of repair and regeneration where the production of new cellular subunits (keratinocytes) at the base of the epidermis is offset by the gradual release of terminally differentiated corneocytes from the surface. It is increasingly clear that proteinases (h
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Josh, R. S. "Tailoring potent plant protease inhibitor against helicoverpa armigera proteases." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2014. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/1969.

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Hamill, J. A. "Involvement of proteases and protease inhibitors in potato late blight." Thesis, Queen's University Belfast, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.426731.

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James, Karen Amanda Ellis. "Design, synthesis, and evaluation of novel cysteine protease inhibitors." Diss., Georgia Institute of Technology, 2002. http://hdl.handle.net/1853/30283.

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Lourbakos, Afrodite 1972. "Activation of human protease-activated receptors by proteases from a periodontal pathogen." Monash University, Dept. of Biochemistry and Molecular Biology, 2001. http://arrow.monash.edu.au/hdl/1959.1/8876.

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Deo, Shivdeep. "DETECTION OF SECRETED PROTEASES AND A MEMBRANE PROTEASE IN PATHOGENIC ACANTHAMOEBA CULBERTSONI." VCU Scholars Compass, 2011. http://scholarscompass.vcu.edu/etd/256.

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Acanthamoeba culbertsoni (A. culbertsoni) is an amphizoic amoeba that is the causative agent of Granulomatous Amoebic Encephalitis (GAE), an often fatal central nervous system infection that is seen most frequently in severely immunocompromised patients and is characterized by hemorrhagic and necrotic lesions of the brain as well as varying degrees of granuloma formation. A.culbertsoni isolates have also been identified in a few cases of Amoebic Keratitis, a painful, sight-threatening corneal infection that disproportionately affects contact lens users irrespective of immune status. Common fea
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Groll, Michael. "Strukturelle und funktionelle Zusammenhänge und Unterschiede archaebakterieller und eukaryontischer 20S-Proteasome." Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2005. http://dx.doi.org/10.18452/13957.

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In eukaryotes protein degradation is performed by the ubiquitin-proteasome system. The 26S proteasome, a 2.5MDa large multimeric molecular machine, consists of more than 30 subunits and represents the core component of this proteolytic pathway. The complex is assembled from a proteolytically active 20S proteasome and two 19S regulator cap complexes. So far crystal structure, topology and enzymatic mechanism have only been elucidated for the 20S proteasome core particle (CP). CPs are assembled from four stacked rings of seven subunits each, following an alpha7beta7beta7alpha7-stochiometry. The
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Fishovitz, Jennifer. "A Chemical Approach to Distinguish ATP-dependent Proteases." Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1291142553.

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Tiew, Kok-Chuan. "Dengue virus protease inhibitors." Thesis, Wichita State University, 2011. http://hdl.handle.net/10057/6117.

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Dengue virus (DENV) is a major health threat that affects 2.5 billion people, or 40% of the world’s population. However, there are no approved antiviral drugs or vaccines to treat Dengue infection. This thesis describes the design, synthesis and discovery of a new class of inhibitors of DENV NS3 protease. Structure-activity relationship studies have been carried out in order to delineate the structural elements responsible for the activity of this series of compounds. A lead compound suitable for further development has been identified.<br>Thesis (M.S.)--Wichita State University, College of Li
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Libros sobre el tema "Protease"

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Cheronis, J. C., and J. E. Repine, eds. Proteases, Protease Inhibitors and Protease-Derived Peptides. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0.

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Cheronis, John Chris Dion, 1951- and Repine John E, eds. Proteases, protease inhibitors, and protease-derived peptides: Importance in human pathophysiology and therapeutics. Basel: Birkhäuser Verlag, 1993.

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Lendeckel, Uwe, and Nigel M. Hooper, eds. Viral Proteases and Antiviral Protease Inhibitor Therapy. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2348-3.

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1926-, Katunuma Nobuhiko, ed. Medical aspects of proteases and protease inhibitors. Amsterdam: IOS Press, 1997.

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B, Banner Carl D., and Nixon Ralph A, eds. Proteases and protease inhibitors in Alzheimer's disease pathogenesis. New York, N.Y: New York Academy of Sciences, 1992.

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A, Nixon Ralph, Banner Carl D. B, and New York Academy of Sciences., eds. Proteases and protease inhibitors in Alzheimer's disease pathogenesis. New York: NewYork Academy of Sciences, 1992.

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Polgár, László. Mechanisms of protease action. Boca Raton, Fla: CRC Press, 1989.

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Chang, Henry E. HIV protease inhibitor report. 2nd ed. Brooklyn, NY (72 Orange St., #3C, Brooklyn 11201): National AIDS Treatment Advocacy Project, 1996.

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Franke, Lars. Von der Protease zur Peptidsynthase. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-30437-9.

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1953-, Ogden Richard C., and Flexner Charles W. 1956-, eds. Protease inhibitors in AIDS therapy. New York: Marcel Dekker, 2001.

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Capítulos de libros sobre el tema "Protease"

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Powers, James C., Shinjiro Odake, Jozef Oleksyszyn, Hitoshi Hori, Toshihisa Ueda, Bogdan Boduszek, and Chih-Min Kam. "Proteases—Structures, Mechanism and Inhibitors." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 3–18. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_1.

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Steffens, Gerd J., Regina Heinzel-Wieland, Derek Saunders, Bernd Wolf, Arjan Rudolphus, Jan Stolk, Johannes A. Krarnps, and Joop A. Dijkman. "Oxidation Resistant Muteins of Antileukoproteinase as Potential Therapeutic Agents." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 111–21. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_10.

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Colman, Robert W. "Factor XII Activation and Inhibition in Inflammation." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 125–43. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_11.

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Stewart, John M. "The Kinin System in Inflammation." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 145–57. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_12.

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Maeda, Hiroshi, Takaaki Akaike, Yoshifumi Sakata, and Keishi Maruo. "Role of Bradykinin in Microbial Infection: Enhancement of Septicemia by Microbial Proteases and Kinin." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 159–65. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_13.

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Whalley, E. T., and J. C. Cheronis. "Kinin Antagonists as Human Therapeutics." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 167–76. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_14.

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Niedbala, Michael J. "Cytokine Regulation of Endothelial Cell Extracellular Proteolysis." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 179–93. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_15.

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Katunuma, Nobuhiko, Hisao Kakegawa, Yoichi Matsunaga, Takeshi Nikawa, and Eiki Korninami. "Different Functional Share of Individual Lysosomal Cathepsins in Normal and Pathological Conditions." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 195–210. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_16.

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Stewart, John M., and Michael E. Hall. "Neuropeptide Processing in Pathophysiology." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 211–26. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_17.

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Aimes, Ronald T., Sheila M. Nielsen-Preiss, and James P. Quigley. "Resolution of Timp-Free and Timp-Complexed 70kDa Progelatinase from Culture Medium of Rous Sarcoma Virus-Transformed Chicken Embryo Fibroblasts." In Proteases, Protease Inhibitors and Protease-Derived Peptides, 227–43. Basel: Birkhäuser Basel, 1993. http://dx.doi.org/10.1007/978-3-0348-7397-0_18.

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Actas de conferencias sobre el tema "Protease"

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David, Ioan, Ariana Velciov, and Gabriel Bujanca. "THE USE OF BIOENZYMATIC INDICATORS LIKE PROTEASE AND ASPARAGINASE ENZYMES ON BISCUIT PRODUCTS." In 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023v/6.2/s25.55.

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This article presents the rheological study of protease and asparaginase enzymes on dough obtained from white flour used for biscuits. Using alveographic method and falling number method we were able to determine the rheological characteristics of the dough used for biscuits and monitor the effects in the flour and finished products of protease and asparaginase enzymes taking into account different dosages. The technological process of preparing biscuits and crackers using protease and asparaginase becomes more healthy and efficient due to improvements in dough handling, volume and texture of
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Delucchi, DM, AS Benton, and RJ Freishtat. "Protease/Anti-Protease Functional Group Evaluation in Lung Disease." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5426.

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Tanabe, Naoya, Atsuyasu Sato, Tatsushi Mizutani, Yoko Hamakawa, Kiyoshi Uemasu, Susumu Sato, Shigeo Muro, and Toyohiro Hirai. "Protease anti-protease imbalance and small airways disease in COPD." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa4256.

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Tilman, Jessica, Amy Day, Natasha Madge, Peter Barnes, and Louise Donnelly. "Macrophage phenotype does not affect protease anti-protease imbalance in COPD." In Annual Congress 2015. European Respiratory Society, 2015. http://dx.doi.org/10.1183/13993003.congress-2015.pa880.

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Mcelvaney, O. F., T. Asakura, S. Meinig, J. L. Torres-Castillo, R. S. Hagan, C. Gabillard, M. P. Murphy, et al. "Protease-Anti-Protease Compartmentalization in SARS-CoV-2 ARDS: Therapeutic Implications." In American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a3629.

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Satog˘lu Dog˘an, M. Yu¨sra, Andrey Revyakin, Sang Park, Alexandros Pertsinidis, Christopher Brown, Steven Chu, Charles S. Craik, and Arun Majumdar. "A New Platform for Profiling Active Proteases With Single-Molecule Sensitivity." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13383.

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Proteases, such as urokinase plasminogen activator (uPA) and prostate specific antigen (PSA), have been used extensively as biomarkers for cancer. A necessary improvement in diagnostics with proteomics is to use the activity levels of proteases as a signal, as opposed to the total protease content. This will provide a better functional insight into the propagation of cancer, and ultimately could allow us to diagnose cancer at earlier stages. Here, we propose a new platform to capture and measure activity of specific proteases in patient samples, with single-molecule sensitivity.
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Dickson, Eva F., Rebecca L. Goyan, James C. Kennedy, M. Mackay, M. A. K. Mendes, and Roy H. Pottier. "Protease-mediated drug delivery." In Applications of Photonic Technology, edited by Roger A. Lessard and George A. Lampropoulos. SPIE, 2003. http://dx.doi.org/10.1117/12.543446.

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Abdullah, Muhammad, Seher Ansar Khawaja, and Muhammad Farooq. "HIV-1 Protease Cleavages." In 2021 International Conference on Innovative Computing (ICIC). IEEE, 2021. http://dx.doi.org/10.1109/icic53490.2021.9692978.

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McCafferty, Darragh, Kelly Moffitt, and Timothy Ferguson. "Development of the first protease multiplex immunoassay for active neutrophilic serine protease biomarkers." In ERS International Congress 2021 abstracts. European Respiratory Society, 2021. http://dx.doi.org/10.1183/13993003.congress-2021.pa1143.

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Barbosa, Karen Eduarda, and Jorge Alexandre Nogueira Santos. "ANÁLISE DO PAPEL DA ENZIMA HIV- 1 PROTEASE NO CICLO REPLICATIVO DO HIV." In I Congresso Nacional de Microbiologia Clínica On-Line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1197.

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Introdução: De acordo com os dados do boletim epidemiológico do Ministério da Saúde (2020), foram notificados 342.459 casos de infecção pelo vírus HIV no Brasil, entre os períodos de junho de 2007 a junho de 2020, demonstrando uma grande incidência da doença no país. Responsável pela depleção de linfócitos TDC4 +, o tratamento disponível consiste na terapia antirretroviral (HAART), baseada em inibidores de proteases entre os quais destaca-se a HIV-1 protease. Essa enzima é responsável pelo desenvolvimento do vírus, se constituindo num importante alvo farmacológico para o tratamento da AIDS. Ob
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Informes sobre el tema "Protease"

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Adam, Zach, and Eran Pichersky. Degradation of Abnormal Proteins in Chloroplasts of Higher Plants. United States Department of Agriculture, August 1994. http://dx.doi.org/10.32747/1994.7568768.bard.

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In this study we attempted to get a better understanding of processes involved in the degradation of abnormal proteins i chloroplasts. To achieve this goal, we used a number of complementary approaches. We first characterized the expression of the two subunits of Clp protease. We demonstrated that both of them were expressed in chloroplasts in a constitutive fashion, but the expression of the regulatory subunit ClpC was enhanced by light. We generated a mutant the lumenal protein OEE33 which was targeted to the stroma in in vitro experiments. In the wrong compartment it was found unstable, and
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Smith, Jeffrey W. Protease Profiling in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, May 2004. http://dx.doi.org/10.21236/ada430267.

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Smith, Jeffrey W. Protease Profiling in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, May 2003. http://dx.doi.org/10.21236/ada416743.

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Tung, Ching-Hsuan. Protease Mediated Anti-Cancer Therapy. Fort Belvoir, VA: Defense Technical Information Center, August 2006. http://dx.doi.org/10.21236/ada458446.

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Chen, Emily. Diagnosing Breast Cancer Using Protease Fingerprint. Fort Belvoir, VA: Defense Technical Information Center, June 2000. http://dx.doi.org/10.21236/ada383309.

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Karnchanatat, Aphichart. Fibrinolytic enzyme from Sand Warm Perinereis nuntia. Chulalongkorn University, 2013. https://doi.org/10.58837/chula.res.2013.106.

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A protease from sandworms (Perinereis nuntia) was purified by using a combination of ammonium sulfate precipitation, DEAE cellulose and Superdex-200, respectively. The enriched preparation had a specific activity of 355.74 U/mg proteins and a yield of 18.5% total protein. The molecular weight of this protease was estimated to be 37.4 kDa by SDS-15% (w/v) PAGE. The pH stability of this protease is between pH 7-8, and it is stable up to 40 °C. The activity of the enzyme was inhibited by Cu2+ and Co2+, but was enhanced by Ca2+ and Mg2+ ions. Furthermore, protease activity was potently inhibited b
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Rogers, J. (Processing and targeting of the thiol protease aleurain). Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6995327.

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Rogers, J. C. [Processing and targeting of the thiol protease aleurain]. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/6619862.

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Barkan, Alice, and Zach Adam. The Role of Proteases in Regulating Gene Expression and Assembly Processes in the Chloroplast. United States Department of Agriculture, January 2003. http://dx.doi.org/10.32747/2003.7695852.bard.

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Chloroplasts house many biochemical processes that are essential for plant viability. Foremost, among these is photosynthesis, which requires the protein-rich thylakoid membrane system. The activation of chloroplast genes encoding thylakoid membrane proteins and the targeting and assembly of these proteins together with their nuclear-encoded partners are essential for the elaboration of the thylakoid membrane. Several nuclear-encoded proteins that regulate chloroplast gene expression and that mediate the targeting of proteins to the thylakoid membrane have been identified in recent years, and
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ภัทรกุล, กนิษฐา, ไตรรักษ์ พิสิษฐ์กุล, นพดล แสงจันทร์ та Jacquet, Alain. การค้นหาวัคซีนแอนติเจนตัวใหม่ของโรคเลปโตสไปโรซิสโดยอาศัยโปรตีโอมิกส์ของโปรตีนบนผิวเซลล์. คณะแพทยศาสตร์ จุฬาลงกรณ์มหาวิทยาลัย, 2018. https://doi.org/10.58837/chula.res.2018.37.

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โรคเลปโตสไปโรซิสเป็นโรคที่มีการแพร่กระจายในหลายพื้นที่รวมทั้งประเทศไทย มีสาเหตุมาจากเชื้อเลปโตสไปราสายพันธุ์ก่อโรค ซึ่งพยาธิกำเนิดของโรคยังไม่ทราบชัดเจน โปรตีนบนผิวเซลล์เป็นส่วนแรกที่เชื้อสัมผัสกับเซลล์ของโฮสต์และสามารถกระตุ้นระบบภูมิคุ้มกัน จึงเป็นเป้าหมายสำคัญในการพัฒนาวัคซีน การหาโปรตีนบนผิวเซลล์ทั้งหมดจะเป็นข้อมูลสำคัญสำหรับการศึกษาพยาธิกำเนิด และการค้นหาวัคซีนตัวใหม่ งานวิจัยนี้มีจุดมุ่งหมายเพื่อจำแนกโปรตีนบนผิวเซลล์ทั้งหมดของเชื้อเลปโตสไปราสายพันธุ์ก่อโรค Leptospira interrogans serovar Pomona ในการศึกษานี้ใช้ 2 วิธี ในการคัดแยกโปรตีนบนผิวเซลล์ออกจากโปรตีนอื่น ได้แก่ วิธีการย่อยโปรตีนบนผิ
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