Advances in peptide synthesis have allowed for the characterization and creation of proteins essential to bodily function such as insulin. One of the proteins characterized since the late eighties as vital to lung function is known as Lung Surfactant Protein SP-B. This protein is crucial for the expansion and contraction of the alveoli in the lungs as it reduces surface tension and allows for the gas exchange that occurs during respiration. Current knowledge in the medical field indicates that the pharmacological applications available are unable to treat twenty percent of infants suffering from Respiratory Distress Syndrome (RDS). At present, treatment for RDS includes either a modified bovine lung surfactant or a lipid/solvent/detergent mixture dispersion that contains no proteins. As this last option provides room for non-protein treatments I plan to synthesize and characterize oligomeric and polymeric biomimetic materials that will serve as substitutes for lung surfactant protein SP-B. ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31HL072730-01
Application #
6591500
Study Section
Special Emphasis Panel (ZRG1-REB (29))
Program Officer
Colombini-Hatch, Sandra
Project Start
2003-01-04
Project End
2003-08-31
Budget Start
2003-01-04
Budget End
2003-08-31
Support Year
1
Fiscal Year
2003
Total Cost
$17,660
Indirect Cost
Name
University of Massachusetts Amherst
Department
Engineering (All Types)
Type
Schools of Arts and Sciences
DUNS #
153926712
City
Amherst
State
MA
Country
United States
Zip Code
01003
Gharib, Sina A; Altemeier, William A; Van Winkle, Laura S et al. (2013) Matrix metalloproteinase-7 coordinates airway epithelial injury response and differentiation of ciliated cells. Am J Respir Cell Mol Biol 48:390-6
Kassim, Sean Y; Gharib, Sina A; Mecham, Brigham H et al. (2007) Individual matrix metalloproteinases control distinct transcriptional responses in airway epithelial cells infected with Pseudomonas aeruginosa. Infect Immun 75:5640-50