Protein species as diagnostic markers

Standard

Protein species as diagnostic markers. / Steffen , P; Kwiatkowski, Marcel; Robertson, Wesley D; Zarrine-Afsar, Arash; Deterra, Diana; Richter, Verena; Schlüter, Hartmut.

In: J PROTEOMICS, Vol. 134, 16.02.2016, p. 5-18.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Steffen , P, Kwiatkowski, M, Robertson, WD, Zarrine-Afsar, A, Deterra, D, Richter, V & Schlüter, H 2016, 'Protein species as diagnostic markers', J PROTEOMICS, vol. 134, pp. 5-18. https://doi.org/10.1016/j.jprot.2015.12.015

APA

Steffen , P., Kwiatkowski, M., Robertson, W. D., Zarrine-Afsar, A., Deterra, D., Richter, V., & Schlüter, H. (2016). Protein species as diagnostic markers. J PROTEOMICS, 134, 5-18. https://doi.org/10.1016/j.jprot.2015.12.015

Vancouver

Steffen P, Kwiatkowski M, Robertson WD, Zarrine-Afsar A, Deterra D, Richter V et al. Protein species as diagnostic markers. J PROTEOMICS. 2016 Feb 16;134:5-18. https://doi.org/10.1016/j.jprot.2015.12.015

Bibtex

@article{fcbf024b920e4fbf9e93bc56b69559e6,
title = "Protein species as diagnostic markers",
abstract = "UNLABELLED: Many diseases are associated with protein species perturbations. A prominent example of an established diagnostic marker is the glycated protein species of hemoglobin, termed HbA1c. HbA1c concentration is increased in the blood of diabetes mellitus patients due to their poor control of blood glucose levels resulting in an increased non-enzymatic glycosylation of hemoglobin producing HbA1c. This important diagnostic marker is routinely measured in the blood of diabetes patients. As in the case of HbA1c, protein species can mirror pathophysiological events. Shifts in the levels of protein species can be associated with or even be responsible for disease making them well suited as diagnostic markers. However, only a few protein species are currently used as diagnostic markers in routine clinical chemistry laboratories, despite being widely established in clinical proteomics research. This review provides an overview of the biochemical characteristics associated with protein species as well as examples of pathophysiological mechanisms, which cause modifications in the protein species composition, thereby emphasizing the importance of screening for protein markers at the species level. Further, we highlight techniques, which are currently utilized for investigating protein species markers in clinical research.BIOLOGICAL SIGNIFICANCE: The success rate of FDA approved diagnostic protein markers until today is very low compared to the number of published candidate disease markers. It is hypothesized that one important reason is the gene-centric view which is still followed in clinical proteomics: In many investigations proteins are still digested in small peptides thus making it nearly impossible to discriminate between healthy proteins and pathologic proteins causing diseases. Thus this review is focusing on the biochemistry and patho-biochemistry of proteins, is highlighting the need for screening for disease markers on the protein species level and is giving an overview about available techniques.",
author = "P Steffen and Marcel Kwiatkowski and Robertson, {Wesley D} and Arash Zarrine-Afsar and Diana Deterra and Verena Richter and Hartmut Schl{\"u}ter",
note = "Copyright {\textcopyright} 2015 Elsevier B.V. All rights reserved.",
year = "2016",
month = feb,
day = "16",
doi = "10.1016/j.jprot.2015.12.015",
language = "English",
volume = "134",
pages = "5--18",
journal = "J PROTEOMICS",
issn = "1874-3919",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Protein species as diagnostic markers

AU - Steffen , P

AU - Kwiatkowski, Marcel

AU - Robertson, Wesley D

AU - Zarrine-Afsar, Arash

AU - Deterra, Diana

AU - Richter, Verena

AU - Schlüter, Hartmut

N1 - Copyright © 2015 Elsevier B.V. All rights reserved.

PY - 2016/2/16

Y1 - 2016/2/16

N2 - UNLABELLED: Many diseases are associated with protein species perturbations. A prominent example of an established diagnostic marker is the glycated protein species of hemoglobin, termed HbA1c. HbA1c concentration is increased in the blood of diabetes mellitus patients due to their poor control of blood glucose levels resulting in an increased non-enzymatic glycosylation of hemoglobin producing HbA1c. This important diagnostic marker is routinely measured in the blood of diabetes patients. As in the case of HbA1c, protein species can mirror pathophysiological events. Shifts in the levels of protein species can be associated with or even be responsible for disease making them well suited as diagnostic markers. However, only a few protein species are currently used as diagnostic markers in routine clinical chemistry laboratories, despite being widely established in clinical proteomics research. This review provides an overview of the biochemical characteristics associated with protein species as well as examples of pathophysiological mechanisms, which cause modifications in the protein species composition, thereby emphasizing the importance of screening for protein markers at the species level. Further, we highlight techniques, which are currently utilized for investigating protein species markers in clinical research.BIOLOGICAL SIGNIFICANCE: The success rate of FDA approved diagnostic protein markers until today is very low compared to the number of published candidate disease markers. It is hypothesized that one important reason is the gene-centric view which is still followed in clinical proteomics: In many investigations proteins are still digested in small peptides thus making it nearly impossible to discriminate between healthy proteins and pathologic proteins causing diseases. Thus this review is focusing on the biochemistry and patho-biochemistry of proteins, is highlighting the need for screening for disease markers on the protein species level and is giving an overview about available techniques.

AB - UNLABELLED: Many diseases are associated with protein species perturbations. A prominent example of an established diagnostic marker is the glycated protein species of hemoglobin, termed HbA1c. HbA1c concentration is increased in the blood of diabetes mellitus patients due to their poor control of blood glucose levels resulting in an increased non-enzymatic glycosylation of hemoglobin producing HbA1c. This important diagnostic marker is routinely measured in the blood of diabetes patients. As in the case of HbA1c, protein species can mirror pathophysiological events. Shifts in the levels of protein species can be associated with or even be responsible for disease making them well suited as diagnostic markers. However, only a few protein species are currently used as diagnostic markers in routine clinical chemistry laboratories, despite being widely established in clinical proteomics research. This review provides an overview of the biochemical characteristics associated with protein species as well as examples of pathophysiological mechanisms, which cause modifications in the protein species composition, thereby emphasizing the importance of screening for protein markers at the species level. Further, we highlight techniques, which are currently utilized for investigating protein species markers in clinical research.BIOLOGICAL SIGNIFICANCE: The success rate of FDA approved diagnostic protein markers until today is very low compared to the number of published candidate disease markers. It is hypothesized that one important reason is the gene-centric view which is still followed in clinical proteomics: In many investigations proteins are still digested in small peptides thus making it nearly impossible to discriminate between healthy proteins and pathologic proteins causing diseases. Thus this review is focusing on the biochemistry and patho-biochemistry of proteins, is highlighting the need for screening for disease markers on the protein species level and is giving an overview about available techniques.

U2 - 10.1016/j.jprot.2015.12.015

DO - 10.1016/j.jprot.2015.12.015

M3 - SCORING: Journal article

C2 - 26721442

VL - 134

SP - 5

EP - 18

JO - J PROTEOMICS

JF - J PROTEOMICS

SN - 1874-3919

ER -