Mumby S M, Kahn R A, Manning D R, Gilman A G
Proc Natl Acad Sci U S A. 1986 Jan;83(2):265-9. doi: 10.1073/pnas.83.2.265.
Antisera were raised against purified subunits of regulatory GTP-binding proteins (G proteins) and against synthetic peptides that correspond to defined regions of G proteins. Peptide antisera were generated that recognized all alpha or all beta subunits from Gs, Gi, Go, and transducin; others recognized only Gs alpha or Go alpha. Such cross-reaction or complete specificity for a given alpha subunit was not obtained when purified subunits were injected. Peptide antisera were used to identify G protein subunits in selected tissue membrane preparations by immunoblots.
制备了针对调节性GTP结合蛋白(G蛋白)纯化亚基以及与G蛋白特定区域相对应的合成肽的抗血清。产生了能识别来自Gs、Gi、Go和转导素的所有α亚基或所有β亚基的肽抗血清;其他抗血清仅识别Gsα或Goα。当注射纯化亚基时,未获得对给定α亚基的这种交叉反应或完全特异性。通过免疫印迹,使用肽抗血清来鉴定选定组织膜制剂中的G蛋白亚基。