|
|
|
|
|
|
|
|
|
|||
|
|
|
|
|
|
|
|
|
Cystic fibrosis (CF) is one of
the most common autosomal recessive diseases in the
human population. CF as a disease
typically involves several different epithelial tissues. However, the principal clinical problem resulting
in 90% of all CF deaths is that of defective lung function. This disease is a result of mutations in a
single gene coding for the cystic fibrosis transmembrane
conductance regulator (CFTR) protein.
CFTR is a member of the ATP-binding cassette (ABC) family of transmembrane reporter proteins. Hundreds of different individual CFTR
mutations falling into five different functional classes have been identified
including missense mutations, frameshifts,
in-frame deletions, and splicing mutants. However, a single mutation
resulting in deletion of the phenylalanine at position 508 of the protein (∆F508)
accounts for approximately 67% of all known CF patients. This mutation results in improper CFTR
protein folding and trafficking such that functional CFTR does not reach the
cell membrane surface. Experiments in
cell culture that are able to overcome the blockade
of this mutant CFTR from reaching the cell surface indicate that if ∆F508
reaches the cell membrane it functions normally. These findings are claimed in
the published Patent Corporation Treaty Application No. PCT/US00/27443. We are seeking an industrial partner who is
interested in further refinement and commercialization. (Ref: J110) |
||
|
|
|
|
|
|
|
|
«Technology Transfer Office : Sponsored Projects : Dartmouth College |
|||
|
|
||||
|
11 Rope Ferry Road #6210 |
||||
|
Hanover, NH 03755-1404 |
Phone: (603) 646-3027 |
|||
|
|
|
|
Fax: (603) 646-3670 |
|