Fig. 2.
Fig. 2. Expression of wild-type and variant AT cDNA in mammalian cells. COS 7 cells were transiently transfected with pcDNA3 vector constructs containing wild-type (WT), or variant AT cDNAs encoding P, M, V, T, G, or R at position –10, or with deletion (Del) of –10L. Cell lysate (l) and culture supernatants (s) were subsequently immunoprecipitated with polyclonal AT antibody. Mock-transfected COS 7 cells (COS) indicate nonspecific binding in the cell lysates. AT is exported to the supernatant only in cells transfected with the wild-type, -10M, -10V and –10L deletion constructs. The substitution of –10L by P, T, G, or R blocks processing and export of the variant AT proteins, with cell lysates showing the presence of only unprocessed and internally initiated protein. See Results for an interpretation of band sizes.

Expression of wild-type and variant AT cDNA in mammalian cells. COS 7 cells were transiently transfected with pcDNA3 vector constructs containing wild-type (WT), or variant AT cDNAs encoding P, M, V, T, G, or R at position –10, or with deletion (Del) of –10L. Cell lysate (l) and culture supernatants (s) were subsequently immunoprecipitated with polyclonal AT antibody. Mock-transfected COS 7 cells (COS) indicate nonspecific binding in the cell lysates. AT is exported to the supernatant only in cells transfected with the wild-type, -10M, -10V and –10L deletion constructs. The substitution of –10L by P, T, G, or R blocks processing and export of the variant AT proteins, with cell lysates showing the presence of only unprocessed and internally initiated protein. See Results for an interpretation of band sizes.

Close Modal

or Create an Account

Close Modal
Close Modal