Isolation and characterization of the human pulmonary surfactant apoprotein gene
Isolation and characterization of the human pulmonary surfactant apoprotein gene
复制标题
DOI:
10.1038/317361a0
复制
发表时间:
1985
期刊:
影响因子:
64.8
通讯作者:
R. T. White;D. Damm;Judy Miller;K. Spratt;J. Schilling;S. Hawgood;B. Benson;B. Cordell
中科院分区:
文献类型:
--
作者:
R. T. White;D. Damm;Judy Miller;K. Spratt;J. Schilling;S. Hawgood;B. Benson;B. Cordell
Pulmonary surfactant is a phospholipid–protein complex which serves to lower the surface tension at the air–liquid interface in the alveoli of the mammalian lung and is essential for normal respiration1. Inadequate levels of surfactant at birth, a frequent situation in premature infants, results in respiratory failure. In all species examined, surfactant is composed primarily of dipalmitoylphosphatidylcholine and two major protein species of relative molecular mass (Mr) 32,000 (32K) and 10K (refs 2–5). Reconstitutionin vitroof purified 32K pulmonary surfactant apoprotein (PSAP) with synthetic lipids forms a lipoprotein complex that lowers surface tension by spreading to create a thin interfacial film6,7. Here we describe the cloning of the human PSAP gene and complementary DNA, and discuss features of the unusual encoded protein.