Jeremy L Goodin

Summary

Affiliation: Walter Reed Army Medical Center
Country: USA

Publications

  1. ncbi request reprint Yersinia pestis outer membrane type III secretion protein YscC: expression, purification, characterization, and induction of specific antiserum
    Jeremy L Goodin
    Bacteriology Division, US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA
    Protein Expr Purif 40:152-63. 2005
  2. doi request reprint Purification and characterization of a recombinant Yersinia pestis V-F1 "Reversed" fusion protein for use as a new subunit vaccine against plague
    Jeremy L Goodin
    Bacteriology Division, U S Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA
    Protein Expr Purif 76:136-44. 2011
  3. pmc Purification and protective efficacy of monomeric and modified Yersinia pestis capsular F1-V antigen fusion proteins for vaccination against plague
    Jeremy L Goodin
    Bacteriology Division, U S Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA
    Protein Expr Purif 53:63-79. 2007

Detail Information

Publications3

  1. ncbi request reprint Yersinia pestis outer membrane type III secretion protein YscC: expression, purification, characterization, and induction of specific antiserum
    Jeremy L Goodin
    Bacteriology Division, US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA
    Protein Expr Purif 40:152-63. 2005
    ..Regardless of the purification method, either form of the YscC protein failed to elicit a protective immune response against lethal plague challenge with either F1 capsule forming Y. pestis CO92 or the isogenic F1(-)Y. pestis C12...
  2. doi request reprint Purification and characterization of a recombinant Yersinia pestis V-F1 "Reversed" fusion protein for use as a new subunit vaccine against plague
    Jeremy L Goodin
    Bacteriology Division, U S Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA
    Protein Expr Purif 76:136-44. 2011
    ..F1S-V-F1 polymerization characteristics were comparable to the native F1. The purified F1S-V-F1 protein appeared equivalent to F1-V in its ability to be recognized by neutralizing antibodies...
  3. pmc Purification and protective efficacy of monomeric and modified Yersinia pestis capsular F1-V antigen fusion proteins for vaccination against plague
    Jeremy L Goodin
    Bacteriology Division, U S Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA
    Protein Expr Purif 53:63-79. 2007
    ..pestis CO92. Thus, vaccination with F1-V monomer and multimeric forms resulted in significant, and essentially equivalent, protection...