scholarly journals Polyamine-induced Z-DNA conformation in plasmids containing (dA-dC)n.(dG-dT)n inserts and increased binding of lupus autoantibodies to the Z-DNA form of plasmids

1994 ◽  
Vol 298 (2) ◽  
pp. 485-491 ◽  
Author(s):  
T J Thomas ◽  
T Thomas

Blocks of potential Z-DNA-forming (dA-dC)n.(dG-dT)n sequences are ubiquitous in eukaryotic genomes. We examined whether naturally occurring polyamines, putrescine, spermidine and spermine, could provoke the Z-DNA conformation in plasmids pDHf2 and pDHf14 with 23 and 60 bp inserts respectively of (dA-dC)n.(dG-dT)n sequences using an e.l.i.s.a. Spermidine and spermine could provoke Z-DNA conformation in these plasmids, but putrescine was ineffective. For pDHf2 and pDHf14, the concentration of spermidine at the midpoint of B-DNA to Z-DNA transition was 25 microM, whereas that of spermine was 16 microM. Polyamine structural specificity was evident in the ability of spermidine homologues to induce Z-DNA. Inorganic cations, Co(NH3)6(3+) and Ru(NH3)6(3+), were ineffective. Our experiments also showed increased binding of anti-DNA autoantibodies from lupus patients as well as autoimmune MRL-lpr/lpr mice to pDHf2 and pDHf14 in the presence of polyamines. These data demonstrate that small blocks of (dA-dC)n.(dG-dT)n sequences could assume the Z-DNA conformation in the presence of natural polyamines. Increased concentrations of polyamines in the sera of lupus patients might facilitate immune complex-formation involving circulating DNA and anti-Z-DNA antibodies.

1999 ◽  
Vol 91 (1) ◽  
pp. 99-105 ◽  
Author(s):  
Daniel J. Birmingham ◽  
Lee A. Hebert ◽  
Xiao-Ping Shen ◽  
Paul Higgins ◽  
C.Grace Yeh ◽  
...  

2014 ◽  
Vol 55 (5) ◽  
pp. 860-869 ◽  
Author(s):  
Dongxu Fu ◽  
Jeremy Y. Yu ◽  
Mingyuan Wu ◽  
Mei Du ◽  
Ying Chen ◽  
...  

1979 ◽  
Vol 11 (2) ◽  
pp. 127-143
Author(s):  
J. Szabó ◽  
T. Szabó ◽  
T. Tóth ◽  
Gy. Lustyik ◽  
Cs. Balázs

1981 ◽  
pp. 154-180 ◽  
Author(s):  
R. J. Levinsky ◽  
R. Paganelli ◽  
D. M. Robertson ◽  
D. J. Atherton

1981 ◽  
Author(s):  
M A Lamb ◽  
H M Reisner ◽  
H A Cooper ◽  
R H Wagner

Immunoradiometric assays (IRMA) of FVIIIR: Ag from normal and certain variant VWD plasmas have suggested possible antigenic differences in the molecules. Studies reported thus far have used antibody specific for normal FVIIIR: Ag. We have further studied this question of antigenic differences using 2 populations of antibody isolated from an antisera prepared against highly purified human FVIII. Isolated IgG was labeled with [125-I]. The population of labeled IgG “specific” for variant FVIIIR: Ag was separated by immune complex formation with a VWD plasma previously shown, by 2% agarose crossed immunoelectrophoresis, to contain only the lower molecular weight multimers of FVIIIR: Ag. The “specific” labeled IgG was obtained by low pH dissociation and subsequent G-200 chromatography. [125-I] IgG “specific” for normal FVIIIR: Ag was similarly obtained after immune complex formation with pooled normal human plasma. Liquid phase IRMAs were performed using differential precipitation with ammonium sulfate or PEG to separate antigen-antibody complexes from free antibody. Using antibody “specific” for normal FVIIIR: Ag, a lack of parallelism was noted in the dose-response curves of variant plasmas as well as a decrease in maximum antibody bound, as compared to normal. Interestingly, when this antibody was absorbed with the variant VWD plasma and the remaining antibody used in IRMAs, none was bound by either variant or normal plasma.Using antibody “specific” for variant FVIIIR: Ag, a similar lack of parallelism in dose-response curves and a decrease in maximum antibody bound were observed. Therefore rather than antigenic differences as previously implied, these results suggest that the discrepancies noted in IRMAs of variant and normal plasmas are a function of the size of the FVIIIR: Ag multimers.


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