TY - CHAP
T1 - Recent Advances in Biological Single-Molecule Applications of Optical Tweezers and Fluorescence Microscopy
AU - Hashemi Shabestari, M.
AU - Meijering, A.E.C.
AU - Roos, W.H.
AU - Wuite, G.J.L.
AU - Peterman, Erwin
PY - 2017
Y1 - 2017
N2 - Over the past two decades, single-molecule techniques have evolved into robust tools to study many fundamental biological processes. The combination of optical tweezers with fluorescence microscopy and microfluidics provides a powerful single-molecule manipulation and visualization technique that has found widespread application in biology. In this combined approach, the spatial (~ nm) and temporal (~ ms) resolution, as well as the force scale (~ pN) accessible to optical tweezers is complemented with the power of fluorescence microscopy. Thereby, it provides information on the local presence, identity, spatial dynamics, and conformational dynamics of single biomolecules. Together, these techniques allow comprehensive studies of, among others, molecular motors, protein–protein and protein–DNA interactions, biomolecular conformational changes, and mechanotransduction pathways. In this chapter, recent applications of fluorescence microscopy in combination with optical trapping are discussed. After an introductory section, we provide a description of instrumentation together with the current capabilities and limitations of the approaches. Next we summarize recent studies that applied this combination of techniques in biological systems and highlight some representative biological assays to mark the exquisite opportunities that optical tweezers combined with fluorescence microscopy provide.
AB - Over the past two decades, single-molecule techniques have evolved into robust tools to study many fundamental biological processes. The combination of optical tweezers with fluorescence microscopy and microfluidics provides a powerful single-molecule manipulation and visualization technique that has found widespread application in biology. In this combined approach, the spatial (~ nm) and temporal (~ ms) resolution, as well as the force scale (~ pN) accessible to optical tweezers is complemented with the power of fluorescence microscopy. Thereby, it provides information on the local presence, identity, spatial dynamics, and conformational dynamics of single biomolecules. Together, these techniques allow comprehensive studies of, among others, molecular motors, protein–protein and protein–DNA interactions, biomolecular conformational changes, and mechanotransduction pathways. In this chapter, recent applications of fluorescence microscopy in combination with optical trapping are discussed. After an introductory section, we provide a description of instrumentation together with the current capabilities and limitations of the approaches. Next we summarize recent studies that applied this combination of techniques in biological systems and highlight some representative biological assays to mark the exquisite opportunities that optical tweezers combined with fluorescence microscopy provide.
KW - Commercial solutions
KW - DNA–protein interaction
KW - Fluorescence microscopy
KW - Mechanochemistry
KW - Microfluidics
KW - Molecular motors
KW - Optical tweezers
KW - Quadruple optical traps
KW - STED super-resolution microscopy
KW - Single molecule
UR - https://www.scopus.com/pages/publications/85008349796
UR - https://www.scopus.com/pages/publications/85008349796#tab=citedBy
U2 - 10.1016/bs.mie.2016.09.047
DO - 10.1016/bs.mie.2016.09.047
M3 - Chapter
SN - 9780128093108
T3 - Methods in Enzymology
SP - 85
EP - 119
BT - Single-Molecule Enzymology
A2 - Spies, Maria
A2 - Chemla, Yann R.
PB - Elsevier
ER -