Quantifying local heterogeneity of in vivo transport dynamics using stochastic scanning multiphoton multifocal microscopy and segmented spatiotemporal image correlation spectroscopy

2008 ◽  
Author(s):  
Hee Y. Kim ◽  
Justin E. Jureller ◽  
Andrey Kuznetsov ◽  
Louis H. Philipson ◽  
Norbert F. Scherer
2006 ◽  
Vol 84 (6) ◽  
pp. 825-831 ◽  
Author(s):  
Ian R. Bates ◽  
Paul W. Wiseman ◽  
John W. Hanrahan

Live cell imaging is a powerful tool for understanding the function and regulation of membrane proteins. In this review, we briefly discuss 4 fluorescence-microscopy-based techniques for studying the transport dynamics of membrane proteins: fluorescence-correlation spectroscopy, image-correlation spectroscopy, fluorescence recovery after photobleaching, and single-particle and (or) molecule tracking. The advantages and limitations of each approach are illustrated using recent studies of an ion channel and cell adhesion molecules.


2013 ◽  
Vol 85 (17) ◽  
pp. 8080-8084 ◽  
Author(s):  
Marco Travagliati ◽  
Salvatore Girardo ◽  
Dario Pisignano ◽  
Fabio Beltram ◽  
Marco Cecchini

2018 ◽  
Vol 207 ◽  
pp. 409-421 ◽  
Author(s):  
Hirak Chakraborty ◽  
Md. Jafurulla ◽  
Andrew H. A. Clayton ◽  
Amitabha Chattopadhyay

Photobleaching image correlation spectroscopy (pbICS) reveals that membrane cholesterol modulates the oligomeric state of the serotonin1A receptor.


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