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Quantification of Extracellular Matrix Proteins from a Rat Lung Scaffold to Provide a Molecular Readout for Tissue Engineering.


ABSTRACT: Data from ProteomeXchange, PXD ID: PXD001213. File: 20121108_Native_Frac3_Lung01_Run03.mzml. Published as part of . From the Abstract: {{i}} ... To support organ engineering efforts, we developed a targeted proteomics method to extract and quantify extracellular matrix components from tissues. Our method provides more complete and accurate protein characterization than traditional approaches. This is accomplished through the analysis of both the chaotrope-soluble and -insoluble protein fractions, and using recombinantly generated stable isotope labeled peptides for absolute quantification. Using this approach, we have generated seventy-four peptides, representing fifty-six proteins to quantify protein in native (non-decellularized) and decellularized lung matrices. We have focused on proteins of the ECM and additional intracellular proteins that are challenging to remove during the decellularization procedure ... {{/i}}

INSTRUMENT(S): Instrument

ORGANISM(S): Rat

DISEASE(S): Not Available

SUBMITTER: Hill RC, et al.  

PROVIDER: GPM32310006954 | GPMDB |

REPOSITORIES: GPMDB

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Quantification of extracellular matrix proteins from a rat lung scaffold to provide a molecular readout for tissue engineering.

Hill Ryan C RC   Calle Elizabeth A EA   Dzieciatkowska Monika M   Niklason Laura E LE   Hansen Kirk C KC  

Molecular & cellular proteomics : MCP 20150208 4


The use of extracellular matrix (ECM) scaffolds, derived from decellularized tissues for engineered organ generation, holds enormous potential in the field of regenerative medicine. To support organ engineering efforts, we developed a targeted proteomics method to extract and quantify extracellular matrix components from tissues. Our method provides more complete and accurate protein characterization than traditional approaches. This is accomplished through the analysis of both the chaotrope-sol  ...[more]

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