A Fluorescence Correlation Spectrometer for Measurements in Cuvettes

被引:8
作者
Sahoo, Bankanidhi [1 ]
Sil, Timir Baran [1 ]
Karmakar, Biswajit [2 ]
Garai, Kanchan [1 ]
机构
[1] Tata Inst Fundamental Res, Hyderabad, Telangana, India
[2] Saha Inst Nucl Phys, Kolkata, India
关键词
CROSS-CORRELATION SPECTROSCOPY; REFRACTIVE-INDEX; CONFOCAL MICROSCOPY; STANDARD-DEVIATION; AQUEOUS-SOLUTIONS; APOLIPOPROTEIN-E; DENATURED STATE; ALPHA-SYNUCLEIN; DIFFUSION; PROTEINS;
D O I
10.1016/j.bpj.2018.05.038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We have developed a fluorescence correlation spectroscopy (FCS) setup for performing single-molecule measurements on samples inside regular cuvettes. The cuvette FCS uses a horizontally mounted extra-long working distance, 0.7 NA, air objective with a working distance of >1.8 mm instead of a high NA water or oil immersion objective. The performance of the cuvette FCS is found to be highly sensitive to the quality and alignment of the cuvette. The radial resolution and effective observation volume obtained using the optimized setup are similar to nm and 1.8 fL, respectively. The highest molecular brightness and the signal/noise ratio in the autocorrelation data achieved using an aqueous solution of rhodamine B are greater than 44 kHz and 110, respectively. Here, we demonstrate two major advantages of cuvette FCS. For example, the cuvette FCS can be used for measurements over a wide range of temperatures that is beyond the range permitted in the microscope-based FCS. Furthermore, cuvette FCS can be coupled to automatic titrators to study urea-dependent unfolding of proteins with unprecedented accuracy. The ease of use and compatibility with various accessories will enable applications of cuvette FCS in the experiments that are regularly performed in spectrofluorometers but are generally avoided in microscope-based FCS.
引用
收藏
页码:455 / 466
页数:12
相关论文
共 53 条
[1]   Dual channel detection of ultra low concentration of bacteria in real time by scanning fluorescence correlation spectroscopy [J].
Altamore, Ilaria ;
Lanzano, Luca ;
Gratton, Enrico .
MEASUREMENT SCIENCE AND TECHNOLOGY, 2013, 24 (06)
[2]   Fluorescence cross-correlation spectroscopy in living cells [J].
Bacia, K ;
Kim, SA ;
Schwille, P .
NATURE METHODS, 2006, 3 (02) :83-89
[3]   Successful FCS Experiment in Nonstandard Conditions [J].
Banachowicz, Ewa ;
Patkowski, Adam ;
Meier, Gerd ;
Klamecka, Kamila ;
Gapinski, Jacek .
LANGMUIR, 2014, 30 (29) :8945-8955
[4]   Methods to calibrate and scale axial distances in confocal microscopy as a function of refractive index [J].
Besseling, T. H. ;
Jose, J. ;
Van Blaaderen, A. .
JOURNAL OF MICROSCOPY, 2015, 257 (02) :142-150
[5]   Kinetics of conformational fluctuations in DNA hairpin-loops [J].
Bonnet, G ;
Krichevsky, O ;
Libchaber, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8602-8606
[6]   In Vivo Imaging of Single-Molecule Translocation Through Nuclear Pore Complexes by Pair Correlation Functions [J].
Cardarelli, Francesco ;
Gratton, Enrico .
PLOS ONE, 2010, 5 (05)
[7]   Measuring unfolding of proteins in the presence of denaturant using fluorescence correlation spectroscopy [J].
Chattopadhyay, K ;
Saffarian, S ;
Elson, EL ;
Frieden, C .
BIOPHYSICAL JOURNAL, 2005, 88 (02) :1413-1422
[8]   Fluorescence correlation spectroscopy shows that monomeric polyglutamine molecules form collapsed structures in aqueous solutions [J].
Crick, Scott L. ;
Jayaraman, Murali ;
Frieden, Carl ;
Wetzel, Ronald ;
Pappu, Rohit V. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (45) :16764-16769
[9]   Mapping eGFP Oligomer Mobility in Living Cell Nuclei [J].
Dross, Nicolas ;
Spriet, Corentin ;
Zwerger, Monika ;
Mueller, Gabriele ;
Waldeck, Waldemar ;
Langowski, Joerg .
PLOS ONE, 2009, 4 (04)
[10]   FLUORESCENCE CORRELATION SPECTROSCOPY APPLIED TO ROTATIONAL DIFFUSION OF MACROMOLECULES [J].
EHRENBERG, M ;
RIGLER, R .
QUARTERLY REVIEWS OF BIOPHYSICS, 1976, 9 (01) :69-81