Rodolfo Hermans

Dr. Rodolfo Hermans

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2006 in Nature Physics
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Journal Article
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JBJasna Brujić
Jasna Brujić
RHRodolfo Hermans
Rodolfo Hermans
KWKirstin A. Walther
Kirstin A. Walther
JFJulio M. Fernandez
Julio M. Fernandez

1 April 2007 in Biophysical Journal
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Journal Article
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JBJasna Brujić
Jasna Brujić
RHRodolfo Hermans
Rodolfo Hermans
SGSergi Garcia-Manyes
Sergi Garcia-Manyes
KWKirstin A. Walther
Kirstin A. Walther
JFJulio M. Fernandez
Julio M. Fernandez

15 August 2012 in Proceedings of the National Academy of Sciences
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Journal Article
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RBRonen Berkovich
Ronen Berkovich
RHRodolfo Hermans
Rodolfo Hermans
IPIonel Popa
Ionel Popa
GSGuillaume Stirnemann
Guillaume Stirnemann
SGSergi Garcia-Manyes
Sergi Garcia-Manyes
JFJulio M. Fernandez
Julio M. Fernandez
The elastic restoring force of tissues must be able to operate over the very wide range of loading rates experienced by living organisms. It is surprising that even the fastest events involving animal muscle tissues do not surpass a few hundred hertz. We propose that this limit is set in part by the elastic dynamics of tethered proteins extending and relaxing under a changing load. Here we study the elastic dynamics of tethered proteins using a fast force spectrometer with sub-millisecond time resolution, combined with Brownian and Molecular Dynamics simulations. We show that the act of tethering a polypeptide to an object, an inseparable part of protein elasticity in vivo and in experimental setups, greatly reduces the attempt frequency with which the protein samples its free energy. Indeed, our data shows that a tethered polypeptide can traverse its free-energy landscape with a surprisingly low effective diffusion coefficient D eff ∼ 1,200 nm 2 /s. By contrast, our Molecular Dynamics simulations show that diffusion of an isolated protein under force occurs at D eff ∼ 10 8 nm 2 /s. This discrepancy is attributed to the drag force caused by the tethering object. From the physiological time scales of tissue elasticity, we calculate that tethered elastic proteins equilibrate in vivo with D eff ∼ 10 4 –10 6 nm 2 /s which is two to four orders magnitude smaller than the values measured for untethered proteins in bulk.

1 June 2003 in Surface Science
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Journal Article
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PLPatricio Lagos L
Patricio Lagos L
RHRodolfo Hermans
Rodolfo Hermans
NVNicolás Velasco
Nicolás Velasco
GTGuido Tarrach
Guido Tarrach
FSFrank Schlaphof
Frank Schlaphof
LELukas M. Eng
Lukas M. Eng

5 November 2001 in Applied Physics Letters
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Journal Article
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GTG. Tarrach
G. Tarrach
PLP. Lagos L.
P. Lagos L.
RHRodolfo Hermans
Rodolfo Hermans
FSF. Schlaphof
F. Schlaphof
CLCh. Loppacher
Ch. Loppacher
LEL. M. Eng
L. M. Eng
We report the 100% correlation between polarized light microscopy (PLM), piezoresponse force microscopy (PFM), and micro-Raman spectroscopy when investigating domain-rich ferroelectric systems. In order to allocate the desired spot on a submicrometer scale, both PLM and PFM were combined to elucidate the effective three-dimensional ferroelectric domain distribution. With PFM we observe spike-like a and c domains well inside extended a and c-polarized areas, which were not conclusive with PLM. The knowledge on such a domain distribution is essential when addressing quantitative micro-Raman spectroscopy. In addition, we show the unambiguous differentiation between a and c domains on the submicrometer scale using the B2 mode of lattice vibrations.

5 March 2020 in Laser & Photonics Reviews
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Journal Article
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LHLucy L. Hale
Lucy L. Hale
JKJanine Keller
Janine Keller
TSThomas Siday
Thomas Siday
RHRodolfo Hermans
Rodolfo Hermans
JHJohannes Haase
Johannes Haase
OMOleg Mitrofanov
Oleg Mitrofanov