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Sökning: onr:"swepub:oai:DiVA.org:kth-126285" > Profiling post-cent...

Profiling post-centrifugation delay of serum and plasma with antibody bead arrays

Qundos, Ulrika (författare)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
Hong, Mun-Gwan (författare)
KTH,Science for Life Laboratory, SciLifeLab
Tybring, Gunnel (författare)
Karolinska Institutet
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Divers, Mark (författare)
Odeberg, Jacob (författare)
KTH,Science for Life Laboratory, SciLifeLab
Uhlén, Mathias (författare)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
Nilsson, Peter (författare)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
Schwenk, Jochen M. (författare)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
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 (creator_code:org_t)
Elsevier BV, 2013
2013
Engelska.
Ingår i: Journal of Proteomics. - : Elsevier BV. - 1874-3919 .- 1876-7737. ; 95:SI, s. 46-54
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Several biobanking initiatives have emerged to create extensive collections of specimen for biomedical studies and various analytical platforms. An affinity proteomic analysis with antibody suspension bead arrays was conducted to investigate the influence of the pre-analytical time and temperature conditions on blood derived samples. Serum and EDTA plasma prepared from 16 individuals was centrifuged and aliquots were kept either at 4. °C or in ambient temperature for 1. h and up to 36. h prior to first storage. Multiplexed protein profiles of post-centrifugation delay were generated in 384 biotinylated samples using 373 antibodies that targeted 343 unique proteins. Very few profiles were observed as significantly altered by the studied temperature and time intervals. Single binder and sandwich assays revealed decreasing levels of caldesmon 1 (CALD1) related to EDTA standard tubes and prolonged post-centrifugation delay of 36. h. Indications from changes in CALD1 levels require further confirmation in independent material, but the current data suggests that samples should preferentially be frozen during the day of collection when to be profiled with antibody arrays selected for this study. Biological significance: Affinity-based profiling of serum and plasma by microarray assays can provide unique opportunities for the discovery of biomarkers. It is though often not known how differences in sample handling after collection influence the downstream analysis. By profiling three types of blood preparations for alterations in protein profiles with respect to time and temperature post centrifugation, we addressed an important component in the analysis and of such specimen. We believe that this analysis adds valuable information to be considered when biobanking blood derived samples.This article is part of a Special Issue entitled: Standardization and Quality Control in Proteomics.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology (hsv//eng)

Nyckelord

protein profiling
plasma
antibody
affinity proteomics
biomark- ers
multiplex
assay development

Publikations- och innehållstyp

ref (ämneskategori)
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