Frank Heinrich

Associate Research Professor

Carnegie Mellon University

United States

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Frank Heinrich is an Associate Research Professor at Carnegie Mellon University, USA. His research focuses on biophysical properties of membrane interactions, cholesterol effects on lipid bilayers, and antimicrobial peptide mechanisms. Recent publications include studies on the conformational flexibility of Myr-Arf1, the entropic behaviors of membrane-bound KRAS, and innovative approaches in neutron reflectometry for data acquisition.

Articles (14)

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2025

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2024

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2024

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2022

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2020

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2020

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2020

Collaborators (3)

Anja Penk

Leipzig University

GERMANY

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Mathias Lösche

Carnegie Mellon University

UNITED STATES

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Stephanie Tristram-Nagle

Carnegie Mellon University

UNITED STATES

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Frank Heinrich

Research Interests

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Articles (14)

The effect of cholesterol on the bending modulus of DOPC bilayers: re-analysis of NSE data

AutoRefl: active learning in neutron reflectometry for fast data acquisition

Novel non-helical antimicrobial peptides insert into and fuse lipid model membranes

Myr-Arf1 conformational flexibility at the membrane surface sheds light on the interactions with ArfGAP ASAP1

Structural and biophysical properties of farnesylated KRas interacting with the chaperone SmgGDS-558

Membrane-bound KRAS approximates an entropic ensemble of configurations

Membrane-bound KRAS approximates an entropic ensemble of configurations

Copper-binding anticancer peptides from the piscidin family: an expanded mechanism that encompasses physical and chemical bilayer disruption

Membrane surface recognition by the ASAP1 PH domain and consequences for interactions with the small GTPase Arf1

Steering Molecular Dynamics Simulations of Membrane-Associated Proteins with Neutron Reflection Results

Synergistic Biophysical Techniques Reveal Structural Mechanisms of Engineered Cationic Antimicrobial Peptides in Lipid Model Membranes.

Membrane surface recognition by the ASAP1 PH domain and consequences for interactions with the small GTPase Arf1

Information gain from isotopic contrast variation in neutron reflectometry on protein–membrane complex structures

Synergistic Biophysical Techniques Reveal Structural Mechanisms of Engineered Cationic Antimicrobial Peptides in Lipid Model Membranes

Collaborators (3)

Anja Penk

Mathias Lösche

Stephanie Tristram-Nagle

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