Dennis R. Burton - La Jolla CA Roberto Burioni - Del Mar CA R. Anthony Williamson - Del Mar CA Pietro P. Sanna - San Diego CA
Assignee:
The Scripps Research Institute - La Jolla CA
International Classification:
C12Q 170
US Classification:
435 5, 435 791, 436518
Abstract:
The present invention provides a novel method for the identification and clonal isolation of antibodies that bind to unique epitopes. The method is based on the use of antibodies as solid phase capture reagents to bind a known capture antibody epitope, thereby precluding the capture antibody epitope from being presented to a population of antibodies to be screened. The method is particularly suited for screening libraries of cloned antibodies, such as phage display combinatorial antibodies. An antibody specific for herpes simplex virus (HSV), was employed as a model for the assay.
The present invention provides a novel method for the identification and clonal isolation of antibodies that bind to unique epitopes. The method is based on the use of antibodies as solid phase capture reagents to bind a known capture antibody epitope, thereby precluding the capture antibody epitope from being presented to a population of antibodies to be screened. The method is particularly suited for screening libraries of cloned antibodies, such as phage display combinatorial antibodies. An antibody specific for herpes simplex virus (HSV), was employed as a model for the assay.
The invention provides methods of preventing or treating drug addiction, or ameliorating the craving for an addictive drug, as well as compounds, peptides, and pharmaceutical compositions that may be used to prevent or treat drug addiction or ameliorate the craving for an addictive drug. The invention also provides methods for identifying agents that may be used to prevent or treat drug addiction, or ameliorate the craving for an addictive drug.
Method For Treatment Of Drug Addiction And For Screening Of Pharmaceutical Agents Therefor
Pietro Sanna - San Diego CA, US George Koob - Encinitas CA, US Serge Ahmed - Bordeaux, FR
International Classification:
A61K 38/20 A61K 38/17
US Classification:
424085200, 514012000
Abstract:
The present invention is directed to a method for treatment of drug addiction and screening methods for identifying pharmaceutical agents that ameloriate or prevent the deleterious effects of addition. The invention is as well directed to a group of genes and a group of gene products that are up or down requested as a result of addiction.
Human Antibodies Neutralizing Human Metapneumovirus
R. Anthony Williamson - La Jolla CA, US Zhifeng Chen - Vista CA, US Pietro Paolo Sanna - San Diego CA, US Dennis R. Burton - La Jolla CA, US James Crowe - Nashville TN, US John V. Williams - Nashville TN, US
The present invention discloses methods for generating antibodies to human metapneumovirus (HMPV) polypeptides, including antibodies that immunospecifically bind to a HMPV F-protein. The invention also discloses methods for preventing, treating, or ameliorating symptoms associated with HMPV infection.
The invention provides methods of preventing or treating drug addiction, or ameliorating the craving for an addictive drug, as well as compounds, peptides, and pharmaceutical compositions that may be used to prevent or treat drug addiction or ameliorate the craving for an addictive drug. The invention also provides methods for identifying agents that may be used to prevent or treat drug addiction, or ameliorate the craving for an addictive drug.
Human Monoclonal Antibodies To Herpes Simplex Virus And Methods Therefor
Dennis R. Burton - La Jolla CA Robert A. Williamson - Del Mar CA Roberto Burioni - Fermignano, IT Pietro Paolo Sanna - San Diego CA
Assignee:
The Scripps Research Institute - La Jolla CA
International Classification:
C07K 1608 A61K 39395 G01N 3353
US Classification:
4241471
Abstract:
The present invention describes human monoclonal antibodies which immunoreact with Herpes simplex virus Type-1 and Type-2. Also disclosed are immunotherapeutic and diagnostic methods of using the monoclonal antibodies, as well as nucleic acids and cell lines for producing the monoclonal antibodies.
Methods And Compositions For Treating Hpa Hyperactivity
Pietro P. SANNA - San Diego CA, US Linda S. LLOYD - San Diego CA, US
International Classification:
C07K 14/575 C07K 14/72
Abstract:
Disclosed are engineered corticotropin-releasing factor (CRF) antagonist agents, including engineered corticotropin-releasing factor (CRF) binding agents. The CRF antagonist agents and binding agents can be used to neutralize excess CRF in vivo and comprise a polypeptide having CRF-specific binding activity under physiological conditions coupled to one or more half-life-extending moieties. Pharmaceutical compositions are disclosed containing the CRF binding agents, which can be used in methods of treatment for diseases, disorders, or conditions involving hypothalamic pituitary adrenal (HPA) axis hyperactivity. Also disclosed are engineered nucleic acids (e.g., expression constructs or vectors) encoding the CRF binding agents and recombinant host cells comprising the engineered nucleic acids.
The Scripps Research Institute
Group Leader at the Scripps Research Institute
Education:
Scripps Research
Skills:
Molecular Biology Biochemistry Cell Biology Animal Models Neuroscience Pharmacology In Vitro Drug Discovery Immunohistochemistry Life Sciences In Vivo Biotechnology Clinical Research Immunology Confocal Microscopy Cell Culture Lifesciences