Differential processing of high-molecular-weight kininogen during normal pregnancy.

TitleDifferential processing of high-molecular-weight kininogen during normal pregnancy.
Publication TypeJournal Article
Year of Publication2020
AuthorsDroll SH, Hsu Y-MSheng, Drake SK, Kim A, Wang W, Calvo KR, Cao Z, Hu TY, Zhao Z
JournalRapid Commun Mass Spectrom
Volume34 Suppl 1
Paginatione8552
Date Published2020 Apr
ISSN1097-0231
KeywordsAdult, Chromatography, Liquid, Female, Humans, Kininogen, High-Molecular-Weight, Peptides, Pregnancy, Proteolysis, Retrospective Studies, Tandem Mass Spectrometry, Young Adult
Abstract

RATIONALE: Studies identified kininogen as a potential biomarker of preeclampsia, a major cause of adverse maternal outcomes. High-molecular-weight kininogen (HK) and its activated form participate in numerous pathways associated with establishing and maintaining pregnancy. However, dynamic changes in HK and naturally occurring HK-derived peptides during the natural course of pregnancy are largely unknown.

METHODS: Longitudinal serum samples during the course of normal pregnancy (trimesters T1, T2, T3) from 60 pregnant women were analyzed by western blot with an anti-HK antibody. Circulating peptides in longitudinal serum specimens derived from 50 participants were enriched using nanoporous silica thin films. Peptides were identified by liquid chromatography/tandem mass spectrometry (LC/MS/MS) and database searching. Relative quantification was performed using MaxQuant and in-house scripts. Normality was evaluated by either ANOVA or Friedman tests with p < 0.05 for statistical significance.

RESULTS: Western blotting revealed that HK significantly decreased during normal pregnancy (T1 vs T2, p < 0.05; T1 vs T3, p < 0.0001). A 100 kDa intermediate increased during pregnancy (T1 vs T2, p < 0.005; T1 vs T3, p < 0.01). Moreover, the heavy chain (T1 vs T2, p < 0.0001; T1 vs T3, p < 0.0001; T2 vs T3, p < 0.01) and light chain (T1 vs T2, p < 0.0001; T1 vs T3, p < 0.0001; T2 vs T3, p < 0.05) significantly increased during pregnancy. LC/MS/MS analysis identified 180 kininogen-1 peptides, of which 167 mapped to domain 5 (D5). Seventy-three peptides with ten or more complete data sets were included for further analysis. Seventy peptides mapped to D5, and 3, 24, and 43 peptides showed significant decrease, no trend, and significant increase, respectively, during pregnancy.

CONCLUSIONS: This study demonstrates dynamic changes in HK and naturally occurring HK-derived peptides during pregnancy. Our study sheds light on the gestational changes of HK and its peptides for further validation of them as potential biomarkers for pregnancy-related complications.

DOI10.1002/rcm.8552
Alternate JournalRapid Commun Mass Spectrom
PubMed ID31412146
PubMed Central IDPMC7018535
Grant ListZ99 CL999999 / ImNIH / Intramural NIH HHS / United States
/ / Weill Cornell Medicine /
Related Faculty: 
Zhen Zhao, Ph.D.

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