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1.
Cell Rep ; 43(4): 114110, 2024 Apr 23.
Artigo em Inglês | MEDLINE | ID: mdl-38607912

RESUMO

Transmembrane transporter proteins are essential for maintaining cellular homeostasis and, as such, are key drug targets. Many transmembrane transporter proteins are known to undergo large structural rearrangements during their functional cycles. Despite the wealth of detailed structural and functional data available for these systems, our understanding of their dynamics and, consequently, how they function is generally limited. We introduce an innovative approach that enables us to directly measure the dynamics and stability of interdomain interactions of transmembrane proteins using optical tweezers. Focusing on the osmoregulatory ATP-binding cassette transporter OpuA from Lactococcus lactis, we examine the mechanical properties and potential interactions of its substrate-binding domains. Our measurements are performed in lipid nanodiscs, providing a native-mimicking environment for the transmembrane protein. The technique provides high spatial and temporal resolution and allows us to study the functionally relevant motions and interdomain interactions of individual transmembrane transporter proteins in real time in a lipid bilayer.


Assuntos
Transportadores de Cassetes de Ligação de ATP , Proteínas de Bactérias , Lactococcus lactis , Pinças Ópticas , Transportadores de Cassetes de Ligação de ATP/metabolismo , Transportadores de Cassetes de Ligação de ATP/química , Lactococcus lactis/metabolismo , Proteínas de Bactérias/metabolismo , Proteínas de Bactérias/química , Ligação Proteica , Domínios Proteicos , Imagem Individual de Molécula , Estabilidade Proteica , Bicamadas Lipídicas/metabolismo , Bicamadas Lipídicas/química
2.
Nanomaterials (Basel) ; 11(9)2021 Sep 17.
Artigo em Inglês | MEDLINE | ID: mdl-34578744

RESUMO

The mechanical properties of proteins can be studied with single molecule force spectroscopy (SMFS) using optical tweezers, atomic force microscopy and magnetic tweezers. It is common to utilize a flexible linker between the protein and trapped probe to exclude short-range interactions in SMFS experiments. One of the most prevalent linkers is DNA due to its well-defined properties, although attachment strategies between the DNA linker and protein or probe may vary. We will therefore provide a general overview of the currently existing non-covalent and covalent bioconjugation strategies to site-specifically conjugate DNA-linkers to the protein of interest. In the search for a standardized conjugation strategy, considerations include their mechanical properties in the context of SMFS, feasibility of site-directed labeling, labeling efficiency, and costs.

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