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Nitrous oxide reductase (N2OR) from Pseudomonas nautica 617, Cabrito, I., Pereira A. S., Tavares P., Besson S., Brondino C., Hoffman B., Brown K., Tegoni M., Cambillau C., Moura J. J. G., and Moura I. , Journal Of Inorganic Biochemistry, Aug, Volume {86}, Number {1}, p.{165}, (2001) Abstract
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Preliminary crystallographic analysis of the oxidized form of a two mono-nuclear iron centres protein from Desulfovibrio desulfuricans ATCC 27774, Coelho, A. V., Matias P. M., Carrondo M. A., Tavares P., Moura J. J. G., Moura I., Fulop V., Hajdu J., and Legall J. , PROTEIN SCIENCE, Jul, Volume {5}, Number {6}, p.{1189-1191}, (1996) Abstract

Crystals of the fully oxidized form of desulfoferrodoxin were obtained by vapor diffusion from a solution containing 20% PEG 4000, 0.1 M HEPES buffer, pH 7.5, and 0.2 M CaCl2. Trigonal and/or rectangular prisms could be obtained, depending on the temperature used for the crystal growth. Trigonal prisms belong to the rhombohedral space group R32, with a = 112.5 Angstrom and c = 63.2 Angstrom; rectangular prisms belong to the monoclinic space group C2, with a = 77.7 Angstrom, b = 80.9 Angstrom, c = 53.9 Angstrom, and beta = 98.1 degrees. The crystallographic asymmetric unit of the rhombohedral crystal form contains one molecule. There are two molecules in the asymmetric unit of the monoclinic form, in agreement with the self-rotation function.

Camelid nanobodies raised against an integral membrane enzyme, nitric oxide reductase, 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, and Desmyter Aline , PROTEIN SCIENCE, Apr, Volume {18}, Number {3}, p.{619-628}, (2009) 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.

Nitric oxide reductase: Direct electrochemistry and electrocatalytic activity, Cordas, Cristina M., Pereira Alice S., Martins Carlos E., Timoteo Cristina G., Moura Isabel, Moura Jose J. G., and Tavares Pedro , Chembiochem, Dec, Volume {7}, Number {12}, p.{1878-1881}, (2006) Abstract
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Comparative electrochemical study of superoxide reductases, Cordas, Cristina M., Raleiras Patricia, Auchère Françoise, Moura Isabel, and Moura Jose J. G. , Eur. Biophys. J., Dec 06, Volume 41, Number 2, p.209-215, (2011) AbstractWebsite

... CM Cordas (&) Á P . Raleiras Á F . Auche`re Á I. Moura Á JJG Moura ... de Quımica, Universidade Nova de Lisboa, 2859-516 Caparica, Portugal e-mail: cristina. cordas @dq.fct ... Present Address: P . Raleiras Department of Photochemistry and Molecular Science, PO Box 523, 75120 ...