蛋白质亚单位
频道(广播)
化学
细胞
分子生物学
细胞生物学
生物
基因
生物化学
计算机科学
计算机网络
作者
M. E. Morton,Tara N. Cassidy,Stanley C. Froehner,Brian P. Gilmour,Robin L. Laurens
标识
DOI:10.1096/fasebj.8.11.8070639
摘要
Monoclonal antibodies that recognize skeletal muscle dihydropyridine‐sensitive calcium channel subunits were used to identify similar proteins in neuronal and small cell carcinoma cell lines. α 1 ‐related proteins were detected by FACS analysis on the surface of human neuroblastoma (IMR 32) and small cell carcinoma (DMS 273 and DMS 114) cell lines. α 1 ‐like polypeptides from these cells were isolated and partially characterized. The polypeptides exhibit an M r similar to that of the L‐type channel α 1 subunit and are recognized by two distinct anti‐ α1 mAbs. The data provide biochemical evidence for structural similarities between the α 1 sub‐unit of small cell carcinoma and neuronal cell lines. Similarly, an α 2 ‐like protein was characterized from these cells. Because α 2 is a subunit shared by many subtypes of calcium channels, these data suggest that subunits other than the pore‐forming α 1 subunit may play an important role in the etiology of Lambert‐Eaton syndrome. We demonstrate directly that small cell carcinoma and a cell line derived from peripheral neurons share L‐type calcium channel‐related proteins and a protein common to many voltage‐gated calcium channel subtypes. These data support a model that proposes that cross‐reactivity of anti‐tumor cell antibodies with presynaptic elements, possibly calcium channels, plays a role in the development of Lambert‐Eaton syndrome.— Morton, M. E., Cassidy, T. N., Froehner, S. C., Gilmour, B. P., Laurens, R. L. α 1 and α 2 Ca 2+ channel subunit expression in human neuronal and small cell carcinoma cells. FASEB J. 8: 884‐888; 1994.
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