User profiles for Stephen R Adams
Stephen AdamsUCSD Verified email at ucsd.edu Cited by 21933 |
The fluorescent toolbox for assessing protein location and function
Advances in molecular biology, organic chemistry, and materials science have recently created
several new classes of fluorescent probes for imaging in cell biology. Here we review the …
several new classes of fluorescent probes for imaging in cell biology. Here we review the …
Specific covalent labeling of recombinant protein molecules inside live cells
BA Griffin, SR Adams, RY Tsien - Science, 1998 - science.org
Recombinant proteins containing four cysteines at the i,i + 1, i + 4, and i + 5 positions of an α
helix were fluorescently labeled in living cells by extracellular administration of 4′,5′-bis(1…
helix were fluorescently labeled in living cells by extracellular administration of 4′,5′-bis(1…
Understanding, improving and using green fluorescent proteins
AB Cubitt, R Heim, SR Adams, AE Boyd… - Trends in biochemical …, 1995 - cell.com
Green fluorescent proteins (GFPs) are presently attracting tremendous interest as the first
general method to create strong visible fluorescence by purely molecular biological means. So …
general method to create strong visible fluorescence by purely molecular biological means. So …
New biarsenical ligands and tetracysteine motifs for protein labeling in vitro and in vivo: synthesis and biological applications
SR Adams, RE Campbell, LA Gross… - Journal of the …, 2002 - ACS Publications
… The intercept of the Perrin plot of FlAsH−Cys 6,7,10,11 -calmodulin indicates a limiting
anisotropy r 0 of 0.35. More significantly, the linearity of the points irrespective of temperature …
anisotropy r 0 of 0.35. More significantly, the linearity of the points irrespective of temperature …
Multicolor and electron microscopic imaging of connexin trafficking
Recombinant proteins containing tetracysteine tags can be successively labeled in living
cells with different colors of biarsenical fluorophores so that older and younger protein …
cells with different colors of biarsenical fluorophores so that older and younger protein …
Fluorescence ratio imaging of cyclic AMP in single cells
SR Adams, AT Harootunian, YJ Buechler, SS Taylor… - Nature, 1991 - nature.com
FLUORESCENCEimaging is perhaps the most powerful technique currently available for
continuously observing the dynamic intracellular biochemistry of single living cells 1 . However, …
continuously observing the dynamic intracellular biochemistry of single living cells 1 . However, …
Controlling cell chemistry with caged compounds
SR Adams, RY Tsien - Annual review of physiology, 1993 - annualreviews.org
" Caged" compounds are artificial molecules whose biological actIvity is controlled by light,
usually by photolytic conversion from an inactive to an active form. The term caged has …
usually by photolytic conversion from an inactive to an active form. The term caged has …
Spatially Resolved Dynamics of cAMP and Protein Kinase A Subunits in Aplysia Sensory Neurons
Cyclic adenosine monophosphate (cAMP)-dependent protein kinase, labeled with fluorescein
and rhodamine on the catalytic and regulatory subunits, respectively, was injected into …
and rhodamine on the catalytic and regulatory subunits, respectively, was injected into …
Activity-dependent regulation of dendritic synthesis and trafficking of AMPA receptors
…, J Tsui, G Gaietta, TJ Deerinck, SR Adams… - Nature …, 2004 - nature.com
Regulation of AMPA receptor (AMPAR) trafficking is important for neural plasticity. Here we
examined the trafficking and synthesis of the GluR1 and GluR2 subunits using ReAsH-EDT 2 …
examined the trafficking and synthesis of the GluR1 and GluR2 subunits using ReAsH-EDT 2 …
A FlAsH-based FRET approach to determine G protein–coupled receptor activation in living cells
C Hoffmann, G Gaietta, M Bünemann, SR Adams… - Nature …, 2005 - nature.com
Fluorescence resonance energy transfer (FRET) from cyan to yellow fluorescent proteins (CFP/YFP)
is a well-established method to monitor protein-protein interactions or …
is a well-established method to monitor protein-protein interactions or …