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Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization

Posttranslational modifications and proteolytic processing regulate almost all physiological processes. Dysregulation can potentially result in pathologic protein species causing diseases. Thus, tissue species proteomes of diseased individuals provide diagnostic information. Since the composition of...

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Autores principales: Kwiatkowski, M., Wurlitzer, M., Krutilin, A., Kiani, P., Nimer, R., Omidi, M., Mannaa, A., Bussmann, T., Bartkowiak, K., Kruber, S., Uschold, S., Steffen, P., Lübberstedt, J., Küpker, N., Petersen, H., Knecht, R., Hansen, N.O., Zarrine-Afsar, A., Robertson, W.D., Miller, R.J.D., Schlüter, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767054/
https://www.ncbi.nlm.nih.gov/pubmed/26778141
http://dx.doi.org/10.1016/j.jprot.2015.12.029
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author Kwiatkowski, M.
Wurlitzer, M.
Krutilin, A.
Kiani, P.
Nimer, R.
Omidi, M.
Mannaa, A.
Bussmann, T.
Bartkowiak, K.
Kruber, S.
Uschold, S.
Steffen, P.
Lübberstedt, J.
Küpker, N.
Petersen, H.
Knecht, R.
Hansen, N.O.
Zarrine-Afsar, A.
Robertson, W.D.
Miller, R.J.D.
Schlüter, H.
author_facet Kwiatkowski, M.
Wurlitzer, M.
Krutilin, A.
Kiani, P.
Nimer, R.
Omidi, M.
Mannaa, A.
Bussmann, T.
Bartkowiak, K.
Kruber, S.
Uschold, S.
Steffen, P.
Lübberstedt, J.
Küpker, N.
Petersen, H.
Knecht, R.
Hansen, N.O.
Zarrine-Afsar, A.
Robertson, W.D.
Miller, R.J.D.
Schlüter, H.
author_sort Kwiatkowski, M.
collection PubMed
description Posttranslational modifications and proteolytic processing regulate almost all physiological processes. Dysregulation can potentially result in pathologic protein species causing diseases. Thus, tissue species proteomes of diseased individuals provide diagnostic information. Since the composition of tissue proteomes can rapidly change during tissue homogenization by the action of enzymes released from their compartments, disease specific protein species patterns can vanish. Recently, we described a novel, ultrafast and soft method for cold vaporization of tissue via desorption by impulsive vibrational excitation (DIVE) using a picosecond-infrared-laser (PIRL). Given that DIVE extraction may provide improved access to the original composition of protein species in tissues, we compared the proteome composition of tissue protein homogenates after DIVE homogenization with conventional homogenizations. A higher number of intact protein species was observed in DIVE homogenates. Due to the ultrafast transfer of proteins from tissues via gas phase into frozen condensates of the aerosols, intact protein species were exposed to a lesser extent to enzymatic degradation reactions compared with conventional protein extraction. In addition, total yield of the number of proteins is higher in DIVE homogenates, because they are very homogenous and contain almost no insoluble particles, allowing direct analysis with subsequent analytical methods without the necessity of centrifugation. BIOLOGICAL SIGNIFICANCE: Enzymatic protein modifications during tissue homogenization are responsible for changes of the in-vivo protein species composition. Cold vaporization of tissues by PIRL-DIVE is comparable with taking a snapshot at the time of the laser irradiation of the dynamic changes that occur continuously under in-vivo conditions. At that time point all biomolecules are transferred into an aerosol, which is immediately frozen.
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spelling pubmed-47670542016-02-29 Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization Kwiatkowski, M. Wurlitzer, M. Krutilin, A. Kiani, P. Nimer, R. Omidi, M. Mannaa, A. Bussmann, T. Bartkowiak, K. Kruber, S. Uschold, S. Steffen, P. Lübberstedt, J. Küpker, N. Petersen, H. Knecht, R. Hansen, N.O. Zarrine-Afsar, A. Robertson, W.D. Miller, R.J.D. Schlüter, H. J Proteomics Article Posttranslational modifications and proteolytic processing regulate almost all physiological processes. Dysregulation can potentially result in pathologic protein species causing diseases. Thus, tissue species proteomes of diseased individuals provide diagnostic information. Since the composition of tissue proteomes can rapidly change during tissue homogenization by the action of enzymes released from their compartments, disease specific protein species patterns can vanish. Recently, we described a novel, ultrafast and soft method for cold vaporization of tissue via desorption by impulsive vibrational excitation (DIVE) using a picosecond-infrared-laser (PIRL). Given that DIVE extraction may provide improved access to the original composition of protein species in tissues, we compared the proteome composition of tissue protein homogenates after DIVE homogenization with conventional homogenizations. A higher number of intact protein species was observed in DIVE homogenates. Due to the ultrafast transfer of proteins from tissues via gas phase into frozen condensates of the aerosols, intact protein species were exposed to a lesser extent to enzymatic degradation reactions compared with conventional protein extraction. In addition, total yield of the number of proteins is higher in DIVE homogenates, because they are very homogenous and contain almost no insoluble particles, allowing direct analysis with subsequent analytical methods without the necessity of centrifugation. BIOLOGICAL SIGNIFICANCE: Enzymatic protein modifications during tissue homogenization are responsible for changes of the in-vivo protein species composition. Cold vaporization of tissues by PIRL-DIVE is comparable with taking a snapshot at the time of the laser irradiation of the dynamic changes that occur continuously under in-vivo conditions. At that time point all biomolecules are transferred into an aerosol, which is immediately frozen. Elsevier 2016-02-16 /pmc/articles/PMC4767054/ /pubmed/26778141 http://dx.doi.org/10.1016/j.jprot.2015.12.029 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kwiatkowski, M.
Wurlitzer, M.
Krutilin, A.
Kiani, P.
Nimer, R.
Omidi, M.
Mannaa, A.
Bussmann, T.
Bartkowiak, K.
Kruber, S.
Uschold, S.
Steffen, P.
Lübberstedt, J.
Küpker, N.
Petersen, H.
Knecht, R.
Hansen, N.O.
Zarrine-Afsar, A.
Robertson, W.D.
Miller, R.J.D.
Schlüter, H.
Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
title Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
title_full Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
title_fullStr Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
title_full_unstemmed Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
title_short Homogenization of tissues via picosecond-infrared laser (PIRL) ablation: Giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
title_sort homogenization of tissues via picosecond-infrared laser (pirl) ablation: giving a closer view on the in-vivo composition of protein species as compared to mechanical homogenization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767054/
https://www.ncbi.nlm.nih.gov/pubmed/26778141
http://dx.doi.org/10.1016/j.jprot.2015.12.029
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