Thermophoretic Manipulation of Molecules inside Living Cells

The complexity of biology requires that measurements of biomolecular interactions be performed inside living cells. While electrophoresis inside cells is prohibited by the cell membrane, the movement of molecules along a temperature gradient appears feasible. This thermophoresis could be used to qua...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the American Chemical Society 2014-11, Vol.136 (45), p.15955-15960
Hauptverfasser: Reichl, Maren R, Braun, Dieter
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The complexity of biology requires that measurements of biomolecular interactions be performed inside living cells. While electrophoresis inside cells is prohibited by the cell membrane, the movement of molecules along a temperature gradient appears feasible. This thermophoresis could be used to quantify binding affinities in vitro at picomolar levels and perform pharmaceutical fragment screens. Here we changed the measurement paradigm to enable measurements inside living cells. The temperature gradient is now applied along the optical axis and measures thermophoretic properties for each pixel of the camera image. We verify the approach for polystyrene beads and DNA of various lengths using finite element modeling. Thermophoresis inside living cells is able to record thermophoretic mobilities and intracellular diffusion coefficients across the whole cytoplasm. Interestingly, we find a 30-fold reduced diffusion coefficient inside the cell, indicating that molecular movement across the cell cytoplasm is slowed down due to molecular crowding.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja506169b