User profiles for "author:Sandra Berndt"

Sandra Berndt

Junior Research Group Leader, Rudolf Schoenheimer Institute of Biochemistry, Leipzig …
Verified email at medizin.uni-leipzig.de
Cited by 338

[HTML][HTML] New structural perspectives in G protein-coupled receptor-mediated Src family kinase activation

S Berndt, I Liebscher - International Journal of Molecular Sciences, 2021 - mdpi.com
Src family kinases (SFKs) are key regulators of cell proliferation, differentiation, and survival.
The expression of these non-receptor tyrosine kinases is strongly correlated with cancer …

[HTML][HTML] Structural basis of arrestin-3 activation and signaling

Q Chen, NA Perry, SA Vishnivetskiy, S Berndt… - Nature …, 2017 - nature.com
A unique aspect of arrestin-3 is its ability to support both receptor-dependent and receptor-
independent signaling. Here, we show that inositol hexakisphosphate (IP6) is a non …

[HTML][HTML] Immunostimulatory effects of targeted thorium-227 conjugates as single agent and in combination with anti-PD-L1 therapy

P Lejeune, V Cruciani, A Berg-Larsen… - … for Immunotherapy of …, 2021 - ncbi.nlm.nih.gov
Background Targeted thorium-227 conjugates (TTCs) are an emerging class of targeted
alpha therapies (TATs). Their unique mode of action (MoA) is the induction of difficult-to …

[HTML][HTML] Antitumor effects of regorafenib and sorafenib in preclinical models of hepatocellular carcinoma

M Kissel, S Berndt, L Fiebig, S Kling, Q Ji, Q Gu… - Oncotarget, 2017 - ncbi.nlm.nih.gov
The purpose of this study was to investigate the antitumor activity of regorafenib and
sorafenib in preclinical models of HCC and to assess their mechanism of action by …

A novel NAMPT inhibitor-based antibody–drug conjugate payload class for cancer therapy

N Böhnke, M Berger, N Griebenow… - Bioconjugate …, 2022 - ACS Publications
Inhibition of intracellular nicotinamide phosphoribosyltransferase (NAMPT) represents a
new mode of action for cancer-targeting antibody–drug conjugates (ADCs) with activity also …

Arrestin-3 scaffolding of the JNK3 cascade suggests a mechanism for signal amplification

NA Perry, TS Kaoud, OO Ortega… - Proceedings of the …, 2019 - National Acad Sciences
Scaffold proteins tether and orient components of a signaling cascade to facilitate signaling.
Although much is known about how scaffolds colocalize signaling proteins, it is unclear …

[HTML][HTML] The N Terminus of Adhesion G Protein–Coupled Receptor GPR126/ADGRG6 as Allosteric Force Integrator

J Mitgau, J Franke, C Schinner, G Stephan… - Frontiers in Cell and …, 2022 - frontiersin.org
The adhesion G protein-coupled receptor (aGPCR) GPR126/ADGRG6 plays an important
role in several physiological functions, such as myelination or peripheral nerve repair. This …

Antibody–drug conjugates with pyrrole‐based KSP inhibitors as the payload class

HG Lerchen, S Wittrock, B Stelte‐Ludwig… - Angewandte Chemie …, 2018 - Wiley Online Library
The number of cytotoxic payload classes successfully employed in antibody–drug
conjugates (ADCs) is still rather limited. The identification of ADC payloads with a novel …

The dark sides of the GPCR tree‐research progress on understudied GPCRs

MM Scharf, LJ Humphrys, S Berndt… - British Journal of …, 2024 - Wiley Online Library
A large portion of the human GPCRome is still in the dark and understudied, consisting even
of entire subfamilies of GPCRs such as odorant receptors, class A and C orphans, adhesion …

An eight amino acid segment controls oligomerization and preferred conformation of the two non-visual arrestins

Q Chen, Y Zhuo, P Sharma, I Perez, DJ Francis… - Journal of molecular …, 2021 - Elsevier
G protein coupled receptors signal through G proteins or arrestins. A long-standing mystery
in the field is why vertebrates have two non-visual arrestins, arrestin-2 and arrestin-3. These …