Search Results - "Demarest, Stephen J."

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    A broad range of Fab stabilities within a host of therapeutic IgGs by Garber, Ellen, Demarest, Stephen J.

    “…Although the functional properties of IgGs are well known, little has been published concerning the stability of whole IgG molecules. Stability is, however, a…”
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    Computationally Designed Bispecific Antibodies using Negative State Repertoires by Leaver-Fay, Andrew, Froning, Karen J., Atwell, Shane, Aldaz, Hector, Pustilnik, Anna, Lu, Frances, Huang, Flora, Yuan, Richard, Hassanali, Saleema, Chamberlain, Aaron K., Fitchett, Jonathan R., Demarest, Stephen J., Kuhlman, Brian

    Published in Structure (London) (05-04-2016)
    “…A challenge in the structure-based design of specificity is modeling the negative states, i.e., the complexes that you do not want to form. This is a difficult…”
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    Engineering a tumor-selective prodrug T-cell engager bispecific antibody for safer immunotherapy by McCue, Amelia C, Demarest, Stephen J, Froning, Karen J, Hickey, Michael J, Antonysamy, Stephen, Kuhlman, Brian

    Published in mAbs (31-12-2024)
    “…T-cell engaging (TCE) bispecific antibodies are potent drugs that trigger the immune system to eliminate cancer cells, but administration can be accompanied by…”
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    Fine Details of IGF-1R Activation, Inhibition, and Asymmetry Determined by Associated Hydrogen /Deuterium-Exchange and Peptide Mass Mapping by Houde, Damian, Demarest, Stephen J.

    Published in Structure (London) (08-06-2011)
    “…The structural features of the asymmetric activated states of the insulin receptor family are still poorly understood. We investigated hydrogen/deuterium…”
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    Generalizable design parameters for soluble T cell receptor-based T cell engagers by Froning, Karen J, Sereno, Arlene, Huang, Flora, Demarest, Stephen J

    Published in Journal for immunotherapy of cancer (01-03-2022)
    “…While most biological and cellular immunotherapies recognize extracellular targets, T cell receptor (TCR) therapeutics are unique in their ability to recognize…”
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    Stability engineering of scFvs for the development of bispecific and multivalent antibodies by Miller, Brian R., Demarest, Stephen J., Lugovskoy, Alexey, Huang, Flora, Wu, Xiufeng, Snyder, William B., Croner, Lisa J., Wang, Norman, Amatucci, Aldo, Michaelson, Jennifer S., Glaser, Scott M.

    Published in Protein engineering, design and selection (01-07-2010)
    “…Single-chain Fvs (scFvs) are commonly used building blocks for creating engineered diagnostic and therapeutic antibody molecules. Bispecific antibodies (BsAbs)…”
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    Mutual synergistic folding in recruitment of CBP/p300 by p160 nuclear receptor coactivators by Wright, Peter E, Demarest, Stephen J, Martinez-Yamout, Maria, Chung, John, Chen, Hongwu, Xu, Wei, Dyson, H. Jane, Evans, Ronald M

    Published in Nature (London) (31-01-2002)
    “…Nuclear hormone receptors are ligand-activated transcription factors that regulate the expression of genes that are essential for development, reproduction and…”
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    Emerging antibody combinations in oncology by Demarest, Stephen J., Hariharan, Kandasamy, Dong, Jianying

    Published in mAbs (01-07-2011)
    “…The use of monoclonal antibodies (mAbs) has become a general approach for specifically targeting and treating human disease. In oncology, the therapeutic…”
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    Building blocks for bispecific and trispecific antibodies by Wu, Xiufeng, Demarest, Stephen J.

    Published in Methods (San Diego, Calif.) (01-02-2019)
    “…Bispecific antibodies (BsAbs), which target two antigens or epitopes, incorporate the specificities and properties of two distinct monoclonal antibodies (mAbs)…”
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    Conserved amino acid networks involved in antibody variable domain interactions by Wang, Norman, Smith, William F., Miller, Brian R., Aivazian, Dikran, Lugovskoy, Alexey A., Reff, Mitchell E., Glaser, Scott M., Croner, Lisa J., Demarest, Stephen J.

    “…Engineered antibodies are a large and growing class of protein therapeutics comprising both marketed products and many molecules in clinical trials in various…”
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    Influence of canonical structure determining residues on antibody affinity and stability by Clark, Louis A., Demarest, Stephen J., Eldredge, John, Jarpe, Matthew B., Li, You, Simon, Ken, van Vlijmen, Herman W.T.

    Published in Journal of structural biology (01-02-2014)
    “…A number of light and heavy chain canonical residue core redesigns were made in a therapeutic antibody (AQC2, anti-VLA1) Fab to explore the consequences to…”
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    Neutralization of Clostridium difficile toxin A using antibody combinations by Demarest, Stephen J., Hariharan, Mangala, Elia, Marikka, Salbato, Jared, Jin, Ping, Bird, Colin, Short, Jay M., Kimmel, Bruce E., Dudley, Michael, Woodnutt, Gary, Hansen, Geneviève

    Published in mAbs (01-03-2010)
    “…The pathogenicity of Clostridium difficile (C. difficile) is mediated by the release of two toxins, A and B. Both toxins contain large clusters of repeats…”
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    Generation of orthogonal Fab-based trispecific antibody formats by Wu, Xiufeng, Yuan, Richard, Bacica, Michael, Demarest, Stephen J

    Published in Protein engineering, design and selection (01-07-2018)
    “…Abstract The clinical success of monoclonal antibodies to treat diseases across nearly every therapeutic area has spurred advances in bispecific antibody…”
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    Packing, specificity, and mutability at the binding interface between the p160 coactivator and CREB‐binding protein by Demarest, Stephen J., Deechongkit, Songpon, Jane Dyson, H., Evans, Ronald M., Wright, Peter E.

    Published in Protein science (01-01-2004)
    “…Among the most common interaction motifs between nuclear proteins is the recognition of one or more amphipathic helices. In an effort to determine principles…”
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