Search Results - "Ste.Marie, Emma J."

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  1. 1

    The Marine Neurotoxin Brevetoxin (PbTx-2) Inhibits Karenia brevis and Mammalian Thioredoxin Reductases by Targeting Different Residues by Colon, Ricardo, Wheater, Michelle, Joyce, Emily J, Ste.Marie, Emma J, Hondal, Robert J, Rein, Kathleen S

    “…The brevetoxins, neurotoxins produced by Karenia brevis, the Florida red tide dinoflagellate, effect fish and wildlife mortalities and adverse public health…”
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    Journal Article
  2. 2

    Aggregation State of Synergistic Antimicrobial Peptides by Remington, Jacob M, Liao, Chenyi, Sharafi, Mona, Ste.Marie, Emma J, Ferrell, Jonathon B, Hondal, Robert J, Wargo, Matthew J, Schneebeli, Severin T, Li, Jianing

    Published in The journal of physical chemistry letters (05-11-2020)
    “…By integrating various simulation and experimental techniques, we discovered that antimicrobial peptides (AMPs) may achieve synergy at an optimal concentration…”
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    Journal Article
  3. 3

    Synthesis of alpha‐methyl selenocysteine and its utilization as a glutathione peroxidase mimic by Wehrle, Robert J., Ste.Marie, Emma J., Hondal, Robert J., Masterson, Douglas S.

    Published in Journal of peptide science (01-06-2019)
    “…Selenocysteine (Sec) is the 21st amino acid in the genetic code where this amino acid is primarily involved in redox reactions in enzymes because of its high…”
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    Journal Article
  4. 4
  5. 5

    2,2′‐Dipyridyl diselenide: A chemoselective tool for cysteine deprotection and disulfide bond formation by Ste.Marie, Emma J., Hondal, Robert J.

    Published in Journal of peptide science (01-03-2020)
    “…There are many examples of bioactive, disulfide‐rich peptides and proteins whose biological activity relies on proper disulfide connectivity. Regioselective…”
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    Journal Article
  6. 6

    Reduction of cysteine‐S‐protecting groups by triisopropylsilane by Ste.Marie, Emma J., Hondal, Robert J.

    Published in Journal of peptide science (01-11-2018)
    “…Triisopropylsilane (TIS), a hindered hydrosilane, has long been utilized as a cation scavenger for the removal of amino acid protecting groups during peptide…”
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    Journal Article
  7. 7

    Facile removal of 4‐methoxybenzyl protecting group from selenocysteine by Jenny, Kaelyn A., Ste.Marie, Emma J., Mose, Gracyn, Ruggles, Erik L., Hondal, Robert J.

    Published in Journal of peptide science (01-10-2019)
    “…Historically, methods to remove the 4‐methoxybenzyl (Mob)–protecting group from selenocysteine (Sec) in peptides have used harsh and toxic reagents. The use of…”
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    Journal Article