Ontology highlight
ABSTRACT:
SUBMITTER: Antoszewski A
PROVIDER: S-EPMC7774804 | biostudies-literature | 2020 Jul
REPOSITORIES: biostudies-literature
Antoszewski Adam A Feng Chi-Jui CJ Vani Bodhi P BP Thiede Erik H EH Hong Lu L Weare Jonathan J Tokmakoff Andrei A Dinner Aaron R AR
The journal of physical chemistry. B 20200625 27
The protein hormone insulin exists in various oligomeric forms, and a key step in binding its cellular receptor is dissociation of the dimer. This dissociation process and its corresponding association process have come to serve as paradigms of coupled (un)folding and (un)binding more generally. Despite its fundamental and practical importance, the mechanism of insulin dimer dissociation remains poorly understood. Here, we use molecular dynamics simulations, leveraging recent developments in umb ...[more]