Region and cell-type resolved quantitative proteomic map of the human heart

Sophia Doll(University of Copenhagen), Martina Dreßen(Deutsches Herzzentrum München), Philipp E. Geyer(University of Copenhagen), Daniel N. Itzhak(Max Planck Institute of Biochemistry), Christian Braun(Ludwig-Maximilians-Universität München), S. Doppler(Deutsches Herzzentrum München), Florian Meier(Max Planck Institute of Biochemistry), Marcus-André Deutsch(German Centre for Cardiovascular Research), Harald Lahm(Deutsches Herzzentrum München), Rüdiger Lange(German Centre for Cardiovascular Research), Markus Krane(German Centre for Cardiovascular Research), Matthias Mann(University of Copenhagen)
Nature Communications
November 7, 2017
Cited by 279Open Access
Full Text

Abstract

The heart is a central human organ and its diseases are the leading cause of death worldwide, but an in-depth knowledge of the identity and quantity of its constituent proteins is still lacking. Here, we determine the healthy human heart proteome by measuring 16 anatomical regions and three major cardiac cell types by high-resolution mass spectrometry-based proteomics. From low microgram sample amounts, we quantify over 10,700 proteins in this high dynamic range tissue. We combine copy numbers per cell with protein organellar assignments to build a model of the heart proteome at the subcellular level. Analysis of cardiac fibroblasts identifies cellular receptors as potential cell surface markers. Application of our heart map to atrial fibrillation reveals individually distinct mitochondrial dysfunctions. The heart map is available at maxqb.biochem.mpg.de as a resource for future analyses of normal heart function and disease.


Related Papers

No related papers found

Powered by citation graph analysis