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@ARTICLE{Frenzel:156269,
author = {Frenzel, Daniel and Willbold, Dieter},
title = {{K}inetic {T}itration {S}eries with {B}iolayer
{I}nterferometry},
journal = {PLoS one},
volume = {9},
number = {9},
issn = {1932-6203},
address = {Lawrence, Kan.},
publisher = {PLoS},
reportid = {FZJ-2014-05060},
pages = {e106882},
year = {2014},
abstract = {Biolayer interferometry is a method to analyze protein
interactions in real-time. In this study, we illustrate the
usefulness to quantitatively analyze high affinity protein
ligand interactions employing a kinetic titration series for
characterizing the interactions between two pairs of
interaction patterns, in particular immunoglobulin G and
protein G B1 as well as scFv IC16 and amyloid beta (1–42).
Kinetic titration series are commonly used in surface
plasmon resonance and involve sequential injections of
analyte over a desired concentration range on a single
ligand coated sensor chip without waiting for complete
dissociation between the injections. We show that applying
this method to biolayer interferometry is straightforward
and i) circumvents problems in data evaluation caused by
unavoidable sensor differences, ii) saves resources and iii)
increases throughput if screening a multitude of different
analyte/ligand combinations.},
cin = {ICS-6},
ddc = {500},
cid = {I:(DE-Juel1)ICS-6-20110106},
pnm = {452 - Structural Biology (POF2-452)},
pid = {G:(DE-HGF)POF2-452},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000342123900015},
pubmed = {pmid:25229647},
doi = {10.1371/journal.pone.0106882},
url = {https://juser.fz-juelich.de/record/156269},
}