Ontology highlight
ABSTRACT:
SUBMITTER: Barcena-Uribarri I
PROVIDER: S-EPMC4081907 | biostudies-other | 2014 Jul
REPOSITORIES: biostudies-other
Bárcena-Uribarri Iván I Thein Marcus M Barbot Mariam M Sans-Serramitjana Eulalia E Bonde Mari M Mentele Reinhard R Lottspeich Friedrich F Bergström Sven S Benz Roland R
The Journal of biological chemistry 20140513 27
P13 is one of the major outer membrane proteins of Borrelia burgdorferi. Previous studies described P13 as a porin. In the present study some structure and function aspects of P13 were studied. P13 showed according to lipid bilayer studies a channel-forming activity of 0.6 nanosiemens in 1 m KCl. Single channel and selectivity measurements demonstrated that P13 had no preference for either cations or anions and showed no voltage-gating up to ±100 mV. Blue native polyacrylamide gel electrophoresi ...[more]