Eli Lilly and Company

Joseph Vincent Manetta

Ying Tang

Derrick Ryan Witcher

Peng Luan

Donmienne Doen Mun Leung

John R Sportsman

William F Heath, Jr

Sau-Chi Betty Yan

Mei-Huei T Lai

Jesse L Bobbitt

Ru-shya Liu

Robert T McCormack

Provided are monoclonal antibodies and antigen-binding fragments thereof that bind to, and inhibit the activity of human FPN1, and which are effective in maintaining or increasing the transport of iron out of mammalian cells and/or maintaining or increasing the level of serum iron, reticulocyte count, red blood cell count, hemoglobin, and/or hematocrit in a subject in vivo.

Anti-ferroportin 1 monoclonal antibodies and uses thereof

A stable xenogeneic fusion partner that is a product of the fusion of a mouse myeloma cell and a non-transformed rabbit partner cell. The fusion partner produces undetectable levels of antibody, as determined by an enzyme linked immunosorbent assay. A method for generating rabbit monoclonal antibodies is disclosed that comprises fusing a nontransformed rabbit partner cell with a rodent myeloma cell to produce a xenogeneic fusion partner, selecting a stable fusion partner producing undetectable levels of antibodies, fusing the stable fusion partner with a rabbit antibody producing cell and isolating an antibody producing cell line that produces antibodies directed to a predetermined antigen.

Stable rabbit-mouse fusion partner

An assay method for the rapid determination of hydrolytic enzyme activity in large numbers of samples is provided which comprises bonding a resin-binding compound, such as biotin, to one side of the scissile bond of the substrate and a reporter molecule, such as a fluorescence marker, to the opposite side of the scissile bond, incubating the modified substrate and the enzyme in multiple well plates, e.g. 96-well plates, optionally in the presence if a test inhibitor or activator compound transferring the incubation solutions to a second multiple well plate having upper and lower chambers separated by a porous membrane the upper chamber of which contains resin beads capable of binding with the resin-binding compound, filtering and washing the wells of the second plate and reading the emission from the plates. The invention also provides protease substrates for HIV-1 protease, vertebrate stromelysin and derivatives thereof which are useful in the assay method.

Substrates for HIV protease

The present invention discloses a new method for solubilizing and refolding recombinant proteins expressed as granules. The method involves sulfitolysis and the formation of a precipitate of protein-S-sulfonate by warming. The precipitate has been found to contain protein in high purity. In addition, proper folding takes place if the desired protein is fully reduced and passed through an intermediate concentration of denaturant which allows for a transition between its folded and unfolded states.

Purification and refolding of recombinant proteins

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Indianapolis, IN, United States of America

Joseph Vincent Manetta