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Brophy, Megan Brunjes. "Bioinorganic Chemistry of the Human Host-Defense Protein Calprotectin". Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/98823.
Pełny tekst źródłaVita. Cataloged from PDF version of thesis.
Includes bibliographical references.
The human innate immune system responds to bacterial and fungal pathogens by releasing the metal-chelating protein calprotectin (CP) at sites of infection and in the upper layers of the epidermis. CP is a Mn(II)- and Zn(ll)-binding protein. The work described in this thesis elucidates the metal-binding properties of CP, and correlates these properties with in vitro growth inhibition of bacteria and fungi. We report that the metal-binding properties of CP are modulated by Ca(ll), and we propose a working model in which CP responds to physiological Ca(Il)-ion gradients to become a potent Zn(ll)- and Mn(Il)-chelating agent in the extracellular space. Individual chapter summaries follow. Chapter 1: Bioinorganic Chemistry of the Host Pathogen Interaction. Transition metal ions are required for all forms of life. During the course of infection, pathogenic microorganisms must acquire transition metals from the host. Three metals of interest from this standpoint are iron, zinc, and manganese. This chapter describes bacterial metal-ion homeostasis machineries, and metal-requiring processes with a focus on Zn(II) and Mn(II). This chapter then highlights the S100 family of Ca(ll)-binding proteins and discuses the Zn(Il)-, Cu(ll)-, and Mn(Il)-binding properties of S100B, S100A12, S100A7, S10OA15, and S100A8/S100A9. Finally, an overview of the scope of this thesis is presented. Chapter 2: Calcium Ion Gradients Modulate the Zinc(Il) Affinity and Antibacterial Activity of Human Calprotectin. Calprotectin (CP) is a human neutrophil protein that is produced and released by neutrophils at sites of infection, where it prevents the growth of microorganisms by sequestering bioavailable zinc(II) and manganese(II). In this chapter, we present metalbinding studies to elucidate the Zn(ll)-binding properties of CP. We report unique optical absorption and EPR spectroscopic signatures for the interfacial His 3Asp and His 4 sites of human CP by using Co(II) as a spectroscopic probe. Zinc competition titrations employing colorimetric and fluorimetric Zn(II) sensors establish that CP coordinates two Zn(II) ions / CP heterodimer. The Ca(ll)-insensitive Zn(ll) sensor ZP4 is used to determine the Kd of CP for Zn(II) in Ca(Il)-deplete and Ca(Il)-replete conditions. These competition titrations afford apparent Kdsitel = 133 58 pM and Kdsite2 = 185 219 nM in the absence of Ca(II). In the presence of excess Ca(Il) these values decrease to Kd,sitel 5 10 pM and Kd,site2 : 240 pM. In vitro antibacterial assays indicate that the metal-binding sites and Ca(ll)-replete conditions are required to inhibit the growth of Gram-negative and Gram-positive bacteria. We propose a model in which Ca(II) ion gradients modulate the antibacterial activity and Zn(Il)-binding properties of human CP. Chapter 3: High-Affinity Manganese Coordination by Human Calprotectin Is Calcium- Dependent and Requires the Histidine-Rich Site at the Dimer Interface. In this chapter, we report that the His 4 motif at the S10OA8/S100A9 dimer interface of CP is required for high-affinity Mn(II) coordination. We identify a low-temperature EPR spectroscopic signal for this site that is consistent with high-spin Mn(II) in an octahedral coordination sphere. This site could be simulated with zero-field splitting parameters D = 270 MHz and EID = 0.30 (E = 81 MHz). This analysis, combined with studies of mutant proteins, suggests that (A8)Hisl7, (A8)His27, (A9)His9l, (A9)His95 and two as-yet unidentified ligands coordinate Mn(ll) at site 2. These studies support a model in which CP responds to Ca(ll) ion gradients to become a potent metal-ion chelator in the extracellular space. Chapter 4: Contributions of the C-terminal Tail of S100A9 to High-Affinity Manganese Binding by Human Calprotectin. This chapter examines the role of the S100A9 C-terminal tail to high-affinity Mn(ll) coordination by human CP. We present a 16-member mutant family with mutations in the S100A9 C-terminal tail (residues 96-114), which houses three histidine and four acidic residues, to evaluate its contribution to Mn(ll) sequestration. These studies confirm that two His residues at positions 103 and 105 complete the octahedral coordination sphere of CP in solution. Appendix 1: Sequence Alignments of Transition-Metal Binding S100 Proteins. Sequence alignments of S100A7, S100A8, S100A9, S100A12, S100A15, and S100B proteins from multiple organisms are presented. Appendix 2: Characterization of CP Mutant Proteins by Circular Dichroism and Analytical Size Exclusion Chromatography. Additional characterization of CP and mutant proteins employed in Chapters 2-4 is presented. Appendix 3: Structures of Sensors Used In this Work. The structures of Zincon, MagFura-2, Zinpyr-1, and Zinpyr-4 are presented. Appendix 4: Manganese Binding Properties of Human Calprotectin under Conditions of High and Low Calcium. This appendix represents a collaborative work with the Drennan Lab (MIT) and Britt Lab (UC Davis) to study the Mn(Il)-CP complex in low- and high-Ca(II) conditions. We report a crystal structure of Mn(Il)-, Ca(Il)-, and Na(l)-bound CP with Mn(II) exclusively coordinated to the His6 motif. Electron spin-echo envelope modulation and electron-nuclear double resonance experiments demonstrate that the six coordinating histidine residues are spectroscopically equivalent. The observed 15N ( = %/h)y perfine couplings (A) arise from two distinct classes of nitrogen atoms: the coordinating E-nitrogen of the imidazole ring of each histidine (A = [3.45, 3.71, 5.91] MHz) and the distal 6-nitrogen (A = [0.11, 0.18, 0.42] MHz). In the absence of Ca(II), the affinity of CP for Mn(II) drops by two to three orders of magnitude, and Mn(II) coordinates to the His6 site as well as other sites on the protein.
by Megan Brunjes Brophy.
Ph. D. in Biological Chemistry
Yan, Siu-cheong. "Bioinorganic chemistry of antimony : interaction of antimonial with biomolecules /". View the Table of Contents & Abstract, 2004. http://sunzi.lib.hku.hk/hkuto/record/B30575540.
Pełny tekst źródłaSeifert, S., i J. Van Den Hoff. "Annual Report 2004 - Institute of Bioinorganic and Radiopharmaceutical Chemistry". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-28695.
Pełny tekst źródłaSeifert, S., i H. Spies. "Annual Report 2003 - Institute of Bioinorganic and Radiopharmaceutical chemistry". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-28959.
Pełny tekst źródłaJohannsen, Bernd, i Sepp Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 2002". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-29271.
Pełny tekst źródłaJohannsen, Bernd, i Sepp Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 2001". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-29488.
Pełny tekst źródłaSeifert, Sepp, i Bernd Johannsen. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 2000". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-29716.
Pełny tekst źródłaJohannsen, Bernd, i Sepp Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1997". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-30891.
Pełny tekst źródłaSeifert, Sepp, i Bernd Johannsen. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1996". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-31238.
Pełny tekst źródłaSeifert, Sepp, i Bernd Johannsen. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1995". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-31653.
Pełny tekst źródłaJohannsen, Bernd. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1994". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-32143.
Pełny tekst źródłaJohannsen, Bernd. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1993". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-32438.
Pełny tekst źródłaJohannsen, Bernd. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1992". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-32587.
Pełny tekst źródłaYan, Siu-cheong, i 甄肇昌. "Bioinorganic chemistry of antimony: interaction of antimonial with biomolecules". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B4457017X.
Pełny tekst źródłaSeifert, S., i J. Van Den Hoff. "Annual Report 2004 - Institute of Bioinorganic and Radiopharmaceutical Chemistry". Forschungszentrum Rossendorf, 2005. https://hzdr.qucosa.de/id/qucosa%3A21696.
Pełny tekst źródłaSeifert, S., i H. Spies. "Annual Report 2003 - Institute of Bioinorganic and Radiopharmaceutical chemistry". Forschungszentrum Rossendorf, 2004. https://hzdr.qucosa.de/id/qucosa%3A21722.
Pełny tekst źródłaJohannsen, Bernd, i Sepp Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 2002". Forschungszentrum Rossendorf, 2003. https://hzdr.qucosa.de/id/qucosa%3A21754.
Pełny tekst źródłaJohannsen, Bernd, i Sepp Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 2001". Forschungszentrum Rossendorf, 2002. https://hzdr.qucosa.de/id/qucosa%3A21775.
Pełny tekst źródłaJohannsen, Bernd, i Sepp Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1997". Forschungszentrum Rossendorf, 1997. https://hzdr.qucosa.de/id/qucosa%3A21916.
Pełny tekst źródłaSeifert, Sepp, i Bernd Johannsen. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1996". Forschungszentrum Rossendorf, 1997. https://hzdr.qucosa.de/id/qucosa%3A21950.
Pełny tekst źródłaSeifert, Sepp, i Bernd Johannsen. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1995". Forschungszentrum Rossendorf, 1996. https://hzdr.qucosa.de/id/qucosa%3A21992.
Pełny tekst źródłaJohannsen, Bernd. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1994". Forschungszentrum Rossendorf, 1995. https://hzdr.qucosa.de/id/qucosa%3A22041.
Pełny tekst źródłaJohannsen, Bernd. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1993". Forschungszentrum Rossendorf, 1994. https://hzdr.qucosa.de/id/qucosa%3A22070.
Pełny tekst źródłaJohannsen, Bernd. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 1992". Forschungszentrum Rossendorf, 1993. https://hzdr.qucosa.de/id/qucosa%3A22085.
Pełny tekst źródłaSeifert, Sepp, i Bernd Johannsen. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Annual Report 2000". Forschungszentrum Rossendorf, 2001. https://hzdr.qucosa.de/id/qucosa%3A21798.
Pełny tekst źródłaJohannsen, B., i S. Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry, Report July - December 1999". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-30041.
Pełny tekst źródłaHowson, Suzanne E. "Self-assembly and bioinorganic chemistry of optically pure helical complexes". Thesis, University of Warwick, 2011. http://wrap.warwick.ac.uk/35728/.
Pełny tekst źródłaJohannsen, B., i S. Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry, Report July - December 1999". Forschungszentrum Rossendorf, 2000. https://hzdr.qucosa.de/id/qucosa%3A21831.
Pełny tekst źródłaGolden, Melissa Lynn. "The bioinorganic chemistry of N2S2 metal complexes: reactivity and ligating ability". Diss., Texas A&M University, 2002. http://hdl.handle.net/1969.1/2198.
Pełny tekst źródłaJohannsen, Bernd, i S. Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Report January 1998 - Juni 1999". Forschungszentrum Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:d120-qucosa-30215.
Pełny tekst źródłaJohannsen, Bernd, i S. Seifert. "Institute of Bioinorganic and Radiopharmaceutical Chemistry; Report January 1998 - Juni 1999". Forschungszentrum Rossendorf, 1999. https://hzdr.qucosa.de/id/qucosa%3A21848.
Pełny tekst źródłaRae, K. J. "The variation of some bioinorganic parameters in rheumatoid arthritis". Thesis, University of Strathclyde, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371978.
Pełny tekst źródłaRazavet, Mathieu. "Synthetic {2Fe3S} assemblies and the active site of all-iron hydrogenases". Thesis, University of East Anglia, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268566.
Pełny tekst źródłaWalton, Paul Howard. "The modelling of copper biosites". Thesis, University of Nottingham, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.276371.
Pełny tekst źródłaKamp, Norbert W. J. "The catalytic oxidation of phenolic substrates using manganese triazacyclononane complexes and hydrogen peroxide". Thesis, University of York, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265366.
Pełny tekst źródłaMars, Craig. "Small molecule models of nitrite reductase". Thesis, University of York, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270037.
Pełny tekst źródłaWagner, William John. "Two Methodologies in Pursuit of the Elucidation of Copper (II)—Centered Bioinorganic Chemistry". [Tampa, Fla] : University of South Florida, 2009. http://purl.fcla.edu/usf/dc/et/SFE0002931.
Pełny tekst źródłaStasser, Jay Paul. "X-ray Absorption Spectroscopy of Copper: Characterization of the Human Copper Chaperone to Superoxide Dismutase". Full text open access at:, 2006. http://content.ohsu.edu/u?/etd,5.
Pełny tekst źródłaLyon, James Thomas III. "Chemical Studies on Oxomolybdenum(VI,IV) Complexes as Bioinorganic Models for the Molybdenum Oxidases". VCU Scholars Compass, 1985. https://scholarscompass.vcu.edu/etd/5227.
Pełny tekst źródłaCronin, Leroy. "Ligand design : new small molecule models for Carbonic Anhydrase". Thesis, University of York, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288064.
Pełny tekst źródłaSchilter, David. "Synthesis and DNA-binding of Metallocyclic Architectures". Thesis, The University of Sydney, 2009. http://hdl.handle.net/2123/5317.
Pełny tekst źródłaSchilter, David. "Synthesis and DNA-binding of Metallocyclic Architectures". University of Sydney, 2009. http://hdl.handle.net/2123/5317.
Pełny tekst źródłaA new family of cationic N-heterocyclic ligand derivatives was prepared and characterised. Among these compounds are halide salts of the dications [Y(spacer)Y]2+, each of which comprise two N heterocyclic donor groups (Y = 4,4′-bipy, pyz, apyz, apym) linked by a conformationally flexible spacer such as (CH2)n, α,α′-xylylene, 2,6-lutidylene or thiabicyclo[3.3.1]nonane-2,6 diyl. The diquaternary halide salts were converted to NO3- and PF6- salts, and interaction of these bridging ligands with labile palladium(II) and platinum(II) precursors afforded several multinuclear complexes. Bis(4,4′-bipyridinium) dications were incorporated into the dinuclear macrocycles [M2(2,2′ bipy)2{4,4′ bipy(CH2)n4,4′-bipy}2]8+ (M = Pd, Pt; n = 4, 6), cis [Pd2Cl4{4,4′ bipy(CH2)34,4′-bipy}2]4+, [Pt2(dppp)2{4,4′-bipy(1,2-xylylene)4,4′-bipy}2]8+ and cis-[Pt2Cl4{4,4′-bipy(1,2-xylylene)4,4′-bipy}2]4+. While bis(pyrazinium) analogues were unreactive towards the palladium(II) and platinum(II) precursors, the doubly deprotonated bis(3 aminopyrazinium) and bis(2 aminopyrimidinium) derivatives served as charge-neutral quadruply-bridging ligands in the complexes [Pt4(2,2′ bipy)4{apyz(CH2)6apyz–2H}2]8+ and [Pt4(2,2′ bipy)4{apym(CH2)5apym–2H}2]8+, both of which feature Pt(II). Pt(II) interactions. Larger species formed when the diamine O,O′-bis(2-aminoethyl)octadeca(ethylene glycol) (PEGda) was treated with cis dinitratopalladium(II) and platinum(II) precursors. The resulting complexes [M(N,N)(PEGda)]2+ (M = Pd, Pt; N,N = 2,2′-bipy, en, tmeda) possessed great size (62 membered chelate rings) and aqueous solubility. DNA-binding studies were conducted with selected complexes in order to investigate the types of interactions these species might participate in. Equimolar mixtures containing either the 16mer duplex DNA D2 or the single strand D2a and palladium(II)/platinum(II) complexes were prepared and analysed by negative-ion ESI MS. Studies of D2/Pd(II) mixtures suggested extensive fragmentation was occuring, and the use of [Pd(tmeda)(PEGda)]2+ and [Pd2(2,2′-bipy)2{4,4′-bipy(CH2)44,4′-bipy}2]8+ resulted in D2 adducts of [Pd(tmeda)]2+ and [4,4′-bipy(CH2)44,4′-bipy]2+, respectively. Decomposition also occurred when D2a was used, although 1 : 1 adducts were observed with [Pd(tmeda)(PEGda)]2+, [Pd(2,2′ bipy)(PEGda)]2+ and [Pd2(2,2′-bipy)2{4,4′-bipy(CH2)44,4′-bipy}2]8+. The low intensities of these adducts indicated that they are unstable towards ESI MS. Analogous ESI-MS experiments using platinum(II) derivatives were performed and, in contrast to those with palladium(II), indicated that the complexes remained largely intact. ESI-MS analysis of D2/Pt(II) mixtures allowed for the detection of 1 : 1 D2 adducts of [Pt(en)(PEGda)]2+, [Pt(tmeda)(PEGda)]2+ and [Pt2(2,2′-bipy)2{4,4′-bipy(CH2)44,4′-bipy}2]8+. Intensities of the adduct ions suggested the greater charge and aryl surface area allow the dinuclear species to bind D2 most strongly. Both [Pt(2,2′-bipy)(Mebipy)2]4+ and [Pt(2,2′ bipy)(NH3)2]2+ gave rise to 1 : 2 adducts of D2, although the latter was found to be a weaker binder, perhaps owing to its lower charge. Data obtained using 1 : 5 (D2 : complex) mixtures were consistent with the results above and suggested that D2 can bind more molecules of daunomycin than any of the platinum(II) species. Analyses of D2a/Pt(II) mixtures gave results similar to those obtained with D2, although fragmentation was more pronounced, indicating that the nucleobases in D2a play more significant roles in mediating decomposition than those in D2, in which they are paired in a complementary manner. Investigations into the effects of selected platinum(II) complexes on the thermal denaturation of calf-thymus DNA (CT-DNA) in solution were conducted. Both [Pt2(2,2′ bipy)2{4,4′-bipy(CH2)64,4′-bipy}2]8+ and [Pt(2,2′-bipy)(Mebipy)2]4+ greatly stabilised CT-DNA, most likely by intercalation. In contrast, [Pt(tmeda)(PEGda)]2+ and [Pt(en)(PEGda)]2+ (as well as PEGda) caused negligible changes in melting temperature (∆Tm), suggesting that these interact weakly with CT-DNA. Data for [Pt(2,2′ bipy)(PEGda)]2+ and [Pt(2,2′-bipy)(NH3)2]2+ indicated that these species perhaps intercalate CT-DNA, with similar ∆Tm values for both complexes implying that PEGda does not play a major role in binding. While findings from ESI-MS experiments were similar to those from the thermal denaturation experiments, discrepancies between results from the two methods could be found. In particular, fragmentation of cyclic species during ESI-MS caused the binding strength of the species to be underestimated when this method was employed.
Green, Kayla Nalynn. "Immobilized metallodithiolate ligand supports for construction of bioinorganic model complexes". [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-2445.
Pełny tekst źródłaMaugeri, Pearson Thomas Maugeri. "Applications of resonance Raman spectroscopy to the study of bioinorganic macromolecules". The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1512093478871388.
Pełny tekst źródłaValentine, Ann M. (Ann Margaret) 1971. "Bioinorganic hydrocarbon oxidation : mechanistic and kinetic studies of the soluble methane monooxygenase from Methylococcus capsulates (bath)". Thesis, Massachusetts Institute of Technology, 1998. http://hdl.handle.net/1721.1/50508.
Pełny tekst źródłaIncludes bibliographical references (p. 219-233).
Chapter 1. Principles of Small Molecule Activation by Metalloproteins as Exemplified by the Soluble Methane Monooxygenase -- Chapter 2. Small Molecule Binding to the Mixed-Valent Diiron Center of Methane Monooxygenase Hydroxylase from Methylococcus capsulatus (Bath) as Revealed by ENDOR Spectroscopy -- Chapter 3. An EPR Study of the Dinuclear Iron Site in the Soluble Methane Monooxygenase Reduced by One Electron at 77 K: the Effect of Component Interactions and the Binding of Small Molecules to the Dinuclear Ferric Center -- Chapter 4. An Investigation of the Reaction of Diferrous Methane Monooxygenase Hydroxylase with Dioxygen and Substrates by Rapid Freeze- Quench and Stopped-Flow Spectroscopy -- Chapter 5. Oxidation of Radical Clock Substrate Probes by the Soluble Methane Monooxygenase System -- Chapter 6. Tritiated Chiral Alkanes as Probes for the Mechanism of Hydroxylation by the Soluble Methane Monooxygenase.
by Ann M. Valentine.
Ph.D.
Conger, Matthew A. "Spectroscopic Insight into Oxidative Heme Cleavage by the Non-canonical Heme Oxygenase IsdG from Staphylococcus aureus". ScholarWorks @ UVM, 2018. https://scholarworks.uvm.edu/graddis/944.
Pełny tekst źródłaLuo, Haibin. "Biointerfacial studies of nucleic-acid bases using chromatographic and three-dimensional chemometric methods". HKBU Institutional Repository, 2005. http://repository.hkbu.edu.hk/etd_ra/658.
Pełny tekst źródłaOsborn, Maire. "Cellular RNA Targeting by Platinum (II) Anticancer Therapeutics". Thesis, University of Oregon, 2014. http://hdl.handle.net/1794/17920.
Pełny tekst źródłaWilson, Clayton Allan. "Effects of Outer Sphere Mutations on CO Binding to Nickel-Substituted Azurin andImplications for Acetyl Coenzyme A Synthase Substrate Channeling". The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1557165301317548.
Pełny tekst źródłaEkström, Jesper. "Transition Metal Hydrides : Biomimetic Studies and Catalytic Applications". Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-7187.
Pełny tekst źródła