Related Experiment Video
Updated: Mar 15, 2026

In Situ Monitoring of Transiently Formed Molecular Chaperone Assemblies in Bacteria, Yeast, and Human Cells
Published on: September 2, 2019
Division of Labor: ER-Resident BiP Co-Chaperones Match Substrates to Fates Based on Specific Binding Sequences
Daniel N Hebert1, Eugenia M Clerico2, Lila M Gierasch3
1Department of Biochemistry and Molecular Biology, Life Sciences Laboratories, University of Massachusetts Amherst, 240 Thatcher Way, Amherst, MA 01003, USA; Program in Molecular and Cellular Biology, Life Sciences Laboratories, University of Massachusetts Amherst, 240 Thatcher Way, Amherst, MA 01003, USA.
Abstract:
In this issue of Molecular Cell, Behnke et al. (2016) describe a novel cell-based peptide-binding assay and use it to analyze the binding specificities of the endoplasmic reticulum Hsp70 chaperone and its co-chaperones and to probe their different roles in protein quality control.
Related Concept Videos
Protein Complexes with Interchangeable Parts
The SCF ubiquitin ligase is a protein complex of five individual proteins. This complex attaches ubiquitin to other target proteins to mark them for degradation. In order...
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair
Long-patch Base Excision Repair
Molecular Chaperones and Protein Folding
The...
Conserved Binding Sites
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...

