@article {5358, title = {Synthesis of catecholamine conjugates with nitrogen-centered bionucleophiles}, journal = {Bioorganic Chemistry}, volume = {44}, year = {2012}, note = {

Times Cited: 0 Siopa, Filipa Pereira, Alice S. Ferreira, Luisa M. Matilde Marques, M. Branco, Paula S.

}, pages = {19-24}, type = {Journal Article}, abstract = {

The enzymatic (tyrosinase) and chemical (NaIO4, Ag2O or Fremys{\textquoteright}s salt) oxidation of biologically relevant catecholamines, such as dopamine (DA), N-acetyldopamine (NADA) and the Ecstasy metabolites (alpha-MeDA and N-Me-alpha-MeDA) generates the corresponding o-quinone which can be trapped with nitrogen bionucleophiles such as N-acetyl-histidine and imidazole in a regioselective reaction that takes place predominantly at the 6-position of the catecholamine. (C) 2012 Elsevier Inc. All rights reserved.

}, issn = {0045-2068}, doi = {10.1016/j.bioorg.2012.05.002}, url = {://WOS:000313902300003}, author = {Siopa, F. and Pereira, AS and Ferreira, LM and Marques, M. M. and Branco, P.S.} } @article {5337, title = {New spectroscopic and electrochemical insights on a class I superoxide reductase: evidence for an intramolecular electron-transfer pathway}, journal = {Biochemical Journal}, volume = {438}, year = {2011}, note = {

Times Cited: 2 Folgosa, Filipe Cordas, Cristina M. Santos, Joana A. Pereira, Alice S. Moura, Jose J. G. Tavares, Pedro Moura, Isabel Part 3

}, pages = {485-494}, type = {Journal Article}, abstract = {

SORs (superoxide reductases) are enzymes involved in bacterial resistance to reactive oxygen species, catalysing the reduction of superoxide anions to hydrogen peroxide. So far three structural classes have been identified. Class I enzymes have two ironcentre-containing domains. Most studies have focused on the catalytic iron site (centre II), yet the role of centre I is poorly understood. The possible roles of this iron site were approached by an integrated study using both classical and fast kinetic measurements, as well as direct electrochemistry. A new heterometallic form of the protein with a zinc-substituted centre I, maintaining the iron active-site centre II, was obtained, resulting in a stable derivative useful for comparison with the native all-iron from. Second-order rate constants for the electron transfer between reduced rubredoxin and the different SOR forms were determined to be 2.8 x 10(7) M(-1) . s(-1) and 1.3 x 10(6) M(-1) . s(-1) for SOR(Fe(IIII)-Fe(II)) and for SOR(Fe(IIII)-Fe(III)) forms respectively, and 3.2 x 10(6) M(-1) s(-1) for the SOR(Zn(II)-Fe(III)) form. The results obtained seem to indicate that centre I transfers electrons from the putative physiological donor rubredoxin to the catalytic active iron site (intramolecular process). In addition, electrochemical results show that conformational changes are associated with the redox state of centre I, which may enable a faster catalytic response towards superoxide anion. The apparent rate constants calculated for the SOR-mediated electron transfer also support this observation.

}, issn = {0264-6021}, doi = {10.1042/bj20110836}, url = {://WOS:000295182100010}, author = {Folgosa, F and Cordas, C. M. and Santos, J. A. and Pereira, AS and Moura, JJG and Tavares, P. and Moura, I} } @article {5325, title = {Camelid nanobodies raised against an integral membrane enzyme, nitric oxide reductase}, journal = {Protein Science}, volume = {18}, number = {3}, year = {2009}, note = {

Times Cited: 11 Conrath, Katja Pereira, Alice S. Martins, Carlos E. Timoteo, Cristina G. Tavares, Pedro Spinelli, Silvia Kinne, Joerg Flaudrops, Christophe Cambillau, Christian Muyldermans, Serge Moura, Isabel Moura, Jose J. G. Tegoni, Mariella Desmyter, Aline

}, pages = {619-628}, type = {Journal Article}, abstract = {

Nitric Oxide Reductase (NOR) is an integral membrane protein performing the reduction of NO to N(2)O. NOR is composed of two subunits: the large one (NorB) is a bundle of 12 transmembrane helices (TMH). It contains a b type heme and a binuclear iron site, which is believed to be the catalytic site, comprising a heme b and a non-hemic iron. The small subunit (NorC) harbors a cytochrome c and is attached to the membrane through a unique TMH. With the aim to perform structural and functional studies of NOR, we have immunized dromedaries with NOR and produced several antibody fragments of the heavy chain (VHHs, also known as nanobodies (TM)). These fragments have been used to develop a faster NOR purification procedure, to proceed to crystallization assays and to analyze the electron transfer of electron donors. BIAcore experiments have revealed that up to three VHHs can bind concomitantly to NOR with affinities in the nanomolar range. This is the first example of the use of VHHs with an integral membrane protein. Our results indicate that VHHs are able to recognize with high affinity distinct epitopes on this class of proteins, and can be used as versatile and valuable tool for purification, functional study and crystallization of integral membrane proteins.

}, issn = {0961-8368}, doi = {10.1002/pro.69}, url = {://WOS:000264941700013}, author = {Conrath, K. and Pereira, AS and Martins, C. E. and Timoteo, C. G. and Tavares, P. and Spinelli, S. and Kinne, J. and Flaudrops, C. and Cambillau, C and Muyldermans, S. and Moura, I and Moura, JJG and Tegoni, M and Desmyter, A.} } @article {5340, title = {A new type of metal-binding site in cobalt- and zinc-containing adenylate kinases isolated from sulfate-reducers Desulfovibrio gigas and Desulfovibrio desulfuricans ATCC 27774}, journal = {Journal of Inorganic Biochemistry}, volume = {102}, number = {5-6}, year = {2008}, note = {

Times Cited: 7 Gavel, Olga Yu. Bursakov, Sergey A. Di Rocco, Giulia Trincao, Jose Pickering, Ingrid J. George, Graham N. Calvete, Juan J. Shnyrov, Valery L. Brondino, Carlos D. Pereira, Alice S. Lampreia, Jorge Tavares, Pedro Moura, Jose J. G. Moura, Isabel 13th International Conference on Biological Inorganic Chemistry JUL 15-20, 2007 Vienna, AUSTRIA

}, pages = {1380-1395}, type = {Journal Article}, abstract = {

Adenylate kinase (AK) mediates the reversible transfer of phosphate groups between the adenylate nucleotides and contributes to the maintenance of their constant cellular level, necessary for energy metabolism and nucleic acid synthesis. The AK were purified from crude extracts of two sulfate-reducing bacteria (SRB), Desulfovibrio (D.) gigas NCIB 9332 and Desulfovibrio desulfuricans ATCC 27774, and biochemically and spectroscopically characterised in the native and fully cobalt- or zinc-substituted forms. These are the first reported adenylate kinases that bind either zinc or cobalt and are related to the subgroup of metal-containing AK found, in most cases, in Gram-positive bacteria. The electronic absorption spectrum is consistent with tetrahedral coordinated cobalt, predominantly via sulfur ligands, and is supported by EPR. The involvement of three cysteines in cobalt or zinc coordination was confirmed by chemical methods. Extended X-ray absorption fine structure (EXAFS) indicate that cobalt or zinc are bound by three cysteine residues and one histidine in the metal-binding site of the "LID" domain. The sequence (129)Cys-X(5)-His-X(15)-Cys-X(2)-Cys of the AK from D. gigas is involved in metal coordination and represents a new type of binding motif that differs from other known zinc-binding sites of AK. Cobalt and zinc play a structural role in stabilizing the LID domain. (C) 2008 Elsevier Inc. All rights reserved.

}, issn = {0162-0134}, doi = {10.1016/j.jinorgbio.2008.01.023}, url = {://WOS:000256239600042}, author = {Gavel, OY and Bursakov, SA and Di Rocco, G and Trincao, J and Pickering, I. J. and George, GN and Calvete, JJ and Shnyrov, VL and Brondino, CD and Pereira, AS and Lampreia, J and Tavares, P. and Moura, JJG and Moura, I} } @article {5354, title = {Purification, characterization, and preliminary crystallographic study of copper-containing nitrous oxide reductase from Pseudomonas nautica 617}, journal = {Biochemistry}, volume = {39}, number = {14}, year = {2000}, note = {

Times Cited: 52 Prudencio, M Pereira, AS Tavares, P Besson, S Cabrito, I Brown, K Samyn, B Devreese, B Van Beeumen, J Rusnak, F Fauque, G Moura, JJG Tegoni, M Cambillau, C Moura, I

}, pages = {3899-3907}, type = {Journal Article}, abstract = {

The aerobic purification of Pseudomonas nautica 617 nitrous oxide reductase yielded two forms of the enzyme exhibiting different chromatographic behaviors. The protein contains six copper atoms per monomer, arranged in two centers named CUA and Cut. Cut could be neither oxidized nor further reduced under our experimental conditions, and exhibits a 4-line EPR spectrum (g(x)= 2.015, A(x) = 1.5 mT, g(y) = 2.071, A(y) = 2 mT, g(z) = 2.138, A(z) = 7 mT) and a strong absorption at similar to 640 nm. Cu-A can be stabilized in a reduced EPR-silent state and in an oxidized state with a typical 7-line EPR spectrum (g(x) g(y) = 2.021, A(x) = A(y) = 0 T, g(z) =0.178, A(z) = 4 mT) and absorption bands at 480, 540, and similar to 800 nm. The difference between the two purified forms of nitrous oxide reductase is interpreted as a difference in the oxidation state of the CuA center. In form A, CUA is predominantly oxidized (S = 1/2, Cu1.5+-Cu1.5+), while in form B it is mostly in the one-electron reduced state (S = 0, Cu1+-Cu1+). In both forms, Cu-Z remains reduced (S = 1/2). Complete crystallographic data at 2.4 Angstrom indicate that Cu-A is a binuclear site (similar to the site found in cytochrome c oxidase) and Cu-Z is a novel tetracopper cluster [Brown, K., et ai. (2000) Nat. Struct. Biol. (in press)]. The complete amino acid sequence of the enzyme was determined and comparisons made with sequences of other nitrous oxide reductases, emphasizing the coordination of the centers. A 10.3 kDa peptide copurified with both forms of nitrous oxide reductase shows strong homology with proteins of the heat-shock GroES chaperonin family.

}, issn = {0006-2960}, doi = {10.1021/bi9926328}, url = {://WOS:000086478400005}, author = {Prudencio, M and Pereira, AS and Tavares, P. and Besson, S and Cabrito, I and Brown, K and Samyn, B and Devreese, B and VanBeeumen, J and Rusnak, F and Fauque, G and Moura, JJG and Tegoni, M and Cambillau, C and Moura, I} } @article {5348, title = {Direct spectroscopic and kinetic evidence for the involvement of a peroxodiferric intermediate during the ferroxidase reaction in fast ferritin mineralization}, journal = {Biochemistry}, volume = {37}, number = {28}, year = {1998}, note = {

Times Cited: 105 Pereira, AS Small, W Krebs, C Tavares, P Edmondson, DE Theil, EC Huynh, BH

}, pages = {9871-9876}, type = {Journal Article}, abstract = {

Rapid freeze-quench (RFQ) Mossbauer and stopped-flow absorption spectroscopy were used to monitor the ferritin ferroxidase reaction using recombinant (apo) frog M ferritin; the initial transient ferric species could be trapped by the RFQ method using low iron loading (36 Fe2+/ferritin molecule). Biphasic kinetics of ferroxidation were observed and measured directly by the Mossbauer method; a majority (85\%) of the ferrous ions was oxidized at a fast rate of similar to 80 s(-1) and the remainder at a much slower rate of similar to 1.7 s(-1). In parallel with the fast phase oxidation of the Fe2+ ions, a single transient iron species is formed which exhibits magnetic properties (diamagnetic ground state) and Mossbauer parameters (Delta E-Q = 1.08 +/- 0.03 mm/s and delta = 0.62 +/- 0.02 mm/s) indicative of an antiferromagnetically coupled peroxodiferric complex. The formation and decay rates of this transient diiron species measured by the RFQ Mossbauer method match those of a transient blue species (lambda(max) = 650 nm) determined by the stopped-flow absorbance measurement. Thus, the transient colored species is assigned to the same peroxodiferric intermediate. Similar transient colored species have been detected by other investigators in several other fast ferritins (H and M subunit types), such as the human H ferritin and the Escherichia coli ferritin, suggesting a similar mechanism for the ferritin ferroxidase step in all fast ferritins. Peroxodiferric complexes are also formed as early intermediates in the reaction of O-2 With the catalytic diiron centers in the hydroxylase component of soluble methane monooxygenase (MMOH) and in the D84E mutant of the R2 subunit of E. coli ribonucleotide reductase. The proposal that a single protein site, with a structure homologous to the diiron centers in MMOH and R2, is involved in the ferritin ferroxidation step is confirmed by the observed kinetics, spectroscopic properties, and purity of the initial peroxodiferric species formed in the frog M ferritin.

}, issn = {0006-2960}, doi = {10.1021/bi980847w}, url = {://WOS:000074893800001}, author = {Pereira, AS and Small, W and Krebs, C and Tavares, P. and Edmondson, DE and Theil, E. C. and HUYNH, BH} }