% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Fahlke:878111,
author = {Fahlke, Christoph},
title = {{M}embrane {P}hysiology and {B}iophysics—{W}hat {R}emains
to {B}e {D}one?},
journal = {Frontiers in physiology},
volume = {11},
issn = {1664-042X},
address = {Lausanne},
publisher = {Frontiers Research Foundation},
reportid = {FZJ-2020-02638},
pages = {892},
year = {2020},
abstract = {Biological membranes consist of lipid bilayer matrices
enriched with integral membrane proteins and
membrane-associated proteins. They not only define cells and
cell organelles but also represent the main contact area for
intercellular communication, for which membrane transport
and signaling are indispensable. Because of their high
physiological importance and unique physical and chemical
properties, biological membranes have been intensively
studied for over 100 years, and membrane physiology remains
a flourishing and lively research field. Recent years have
witnessed great progress in our understanding of the
biophysical basis of membrane transport and its role in
generating biological electricity and controlling the
intracellular milieu. The workings of ion channels and
transporters are understood in a degree of detail that was
unimaginable when many of us started our scientific careers.
Protein sequences and three-dimensional structures are now
available for almost every major ion channel and transporter
family (Navratna and Gouaux, 2019). Heterologous expression
systems and patch clamp electrophysiology can provide
functional data of unprecedented accuracy (Neher, 1992;
Sakmann, 1992). The identification of amino acid sequences
that direct ion channels and transporters to specific
intracellular membrane compartments has enabled ion
transport proteins that normally reside in intracellular
membranes (such as synaptic vesicles or lysosomes) to be
expressed and studied on the plasma membrane of mammalian
cells (Leisle et al., 2011; Guzman et al., 2015; Eriksen et
al., 2016). Moreover, advances in live-cell imaging enable
the real-time visualization of intracellular trafficking of
ion channels and transporters from protein translation in
the endoplasmic reticulum to their arrival at the plasma
membrane or site of action (Xiao and Shaw, 2015; Conrad et
al., 2018).},
cin = {IBI-1},
ddc = {610},
cid = {I:(DE-Juel1)IBI-1-20200312},
pnm = {552 - Engineering Cell Function (POF3-552)},
pid = {G:(DE-HGF)POF3-552},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32848847},
UT = {WOS:000561341200001},
doi = {10.3389/fphys.2020.00892},
url = {https://juser.fz-juelich.de/record/878111},
}