Optimization of capillary electrophoresisinductively coupled plasma mass spectrometry for species analysis of metallothionein-like proteins extracted from liver tissues of Elbe-bream and Roe deer

Research output: Journal contributionsConference article in journalResearchpeer-review

Standard

Optimization of capillary electrophoresisinductively coupled plasma mass spectrometry for species analysis of metallothionein-like proteins extracted from liver tissues of Elbe-bream and Roe deer. / Pröfrock, Daniel; Prange, Andreas; Schaumlöffel, Dirk et al.

In: Spectrochimica Acta Part B: Atomic Spectroscopy, Vol. 58, No. 8, 15.08.2003, p. 1403-1415.

Research output: Journal contributionsConference article in journalResearchpeer-review

Harvard

APA

Vancouver

Bibtex

@article{bc91d405ed88421897f349898ba0081b,
title = "Optimization of capillary electrophoresisinductively coupled plasma mass spectrometry for species analysis of metallothionein-like proteins extracted from liver tissues of Elbe-bream and Roe deer",
abstract = "Species analysis of metallothionein-like proteins (MLP) in liver tissues from Elbe-Bream (Abramis brama L.) and Roe Deer (Capreolus capreolus L.) using capillary electrophoresis (CE) combined with inductively coupled plasma mass spectrometry detection is described. In order to allow systematic development of the method, commercially available metallothionein (MT) preparations of rabbit liver were used. Optimum separation efficiency was obtained by investigating the influence of parameters such as voltage, capillary temperature, buffer concentration, buffer pH and the use of different buffer systems. Instrumental parameters such as CE capillary position, interface adjustment and contamination problems are also discussed. Separation was performed using uncoated fused silica capillaries with 75 μm i.d. and 70 cm length. The optimum conditions were found to be: Separation voltage 30 kV, positive polarity, capillary temperature 288.15 K and a buffer concentration of 100 mmol l -1 Tricine-NH 3 adjusted to pH 7.2. Sample preparation was performed so as to minimize oxidation and heavy metal contamination of the samples. The high molecular mass protein matrix was reduced by acetonitrile precipitation. For commercial MT preparations the relative standard deviations (R.S.D) in the retention times were 0.9% for MT-1 and 1.9% for MT-2; the R.S.D.'s in the peak areas were less than 6% for MT-1 and 16% for MT-2, respectively. Under optimized conditions the MLPs in the real samples could be separated efficiently in less than 10 min. By comparison with the migration times of commercially available MT preparations, two of the observed peaks could be assigned to MT-1 and MT-2.",
keywords = "Chemistry, Capillary electrophoresis, Inductively coupled plasma mass spectrometry, Metallothionein, Metallothionein-like proteins, Heavy metals, Tricine-buffer",
author = "Daniel Pr{\"o}frock and Andreas Prange and Dirk Schauml{\"o}ffel and Wolfgang Ruck",
year = "2003",
month = aug,
day = "15",
doi = "10.1016/s0584-8547(03)00088-0",
language = "English",
volume = "58",
pages = "1403--1415",
journal = "Spectrochimica Acta, Part B: Atomic Spectroscopy",
issn = "0584-8547",
publisher = "Elsevier B.V.",
number = "8",
note = "5th European Furnace Symposium and 10th International Solid Sampling Colloquium with Atomic Spectrometry - 2002, 5th EFS and 10th International SSC with Atomic Spectrometry - 2002 ; Conference date: 01-09-2002 Through 04-09-2002",
url = "https://esas2020.pl/",

}

RIS

TY - JOUR

T1 - Optimization of capillary electrophoresisinductively coupled plasma mass spectrometry for species analysis of metallothionein-like proteins extracted from liver tissues of Elbe-bream and Roe deer

AU - Pröfrock, Daniel

AU - Prange, Andreas

AU - Schaumlöffel, Dirk

AU - Ruck, Wolfgang

N1 - Conference code: 5

PY - 2003/8/15

Y1 - 2003/8/15

N2 - Species analysis of metallothionein-like proteins (MLP) in liver tissues from Elbe-Bream (Abramis brama L.) and Roe Deer (Capreolus capreolus L.) using capillary electrophoresis (CE) combined with inductively coupled plasma mass spectrometry detection is described. In order to allow systematic development of the method, commercially available metallothionein (MT) preparations of rabbit liver were used. Optimum separation efficiency was obtained by investigating the influence of parameters such as voltage, capillary temperature, buffer concentration, buffer pH and the use of different buffer systems. Instrumental parameters such as CE capillary position, interface adjustment and contamination problems are also discussed. Separation was performed using uncoated fused silica capillaries with 75 μm i.d. and 70 cm length. The optimum conditions were found to be: Separation voltage 30 kV, positive polarity, capillary temperature 288.15 K and a buffer concentration of 100 mmol l -1 Tricine-NH 3 adjusted to pH 7.2. Sample preparation was performed so as to minimize oxidation and heavy metal contamination of the samples. The high molecular mass protein matrix was reduced by acetonitrile precipitation. For commercial MT preparations the relative standard deviations (R.S.D) in the retention times were 0.9% for MT-1 and 1.9% for MT-2; the R.S.D.'s in the peak areas were less than 6% for MT-1 and 16% for MT-2, respectively. Under optimized conditions the MLPs in the real samples could be separated efficiently in less than 10 min. By comparison with the migration times of commercially available MT preparations, two of the observed peaks could be assigned to MT-1 and MT-2.

AB - Species analysis of metallothionein-like proteins (MLP) in liver tissues from Elbe-Bream (Abramis brama L.) and Roe Deer (Capreolus capreolus L.) using capillary electrophoresis (CE) combined with inductively coupled plasma mass spectrometry detection is described. In order to allow systematic development of the method, commercially available metallothionein (MT) preparations of rabbit liver were used. Optimum separation efficiency was obtained by investigating the influence of parameters such as voltage, capillary temperature, buffer concentration, buffer pH and the use of different buffer systems. Instrumental parameters such as CE capillary position, interface adjustment and contamination problems are also discussed. Separation was performed using uncoated fused silica capillaries with 75 μm i.d. and 70 cm length. The optimum conditions were found to be: Separation voltage 30 kV, positive polarity, capillary temperature 288.15 K and a buffer concentration of 100 mmol l -1 Tricine-NH 3 adjusted to pH 7.2. Sample preparation was performed so as to minimize oxidation and heavy metal contamination of the samples. The high molecular mass protein matrix was reduced by acetonitrile precipitation. For commercial MT preparations the relative standard deviations (R.S.D) in the retention times were 0.9% for MT-1 and 1.9% for MT-2; the R.S.D.'s in the peak areas were less than 6% for MT-1 and 16% for MT-2, respectively. Under optimized conditions the MLPs in the real samples could be separated efficiently in less than 10 min. By comparison with the migration times of commercially available MT preparations, two of the observed peaks could be assigned to MT-1 and MT-2.

KW - Chemistry

KW - Capillary electrophoresis

KW - Inductively coupled plasma mass spectrometry

KW - Metallothionein

KW - Metallothionein-like proteins

KW - Heavy metals

KW - Tricine-buffer

UR - http://www.scopus.com/inward/record.url?scp=0042012843&partnerID=8YFLogxK

U2 - 10.1016/s0584-8547(03)00088-0

DO - 10.1016/s0584-8547(03)00088-0

M3 - Conference article in journal

VL - 58

SP - 1403

EP - 1415

JO - Spectrochimica Acta, Part B: Atomic Spectroscopy

JF - Spectrochimica Acta, Part B: Atomic Spectroscopy

SN - 0584-8547

IS - 8

T2 - 5th European Furnace Symposium and 10th International Solid Sampling Colloquium with Atomic Spectrometry - 2002

Y2 - 1 September 2002 through 4 September 2002

ER -