scholarly journals ACTH, cyclic nucleotides, and brain protein phosphorylation in vitro

1976 ◽  
Vol 1 (6) ◽  
pp. 669-677 ◽  
Author(s):  
H. Zwiers ◽  
H. D. Veldhuis ◽  
P. Schotman ◽  
W. H. Gispen
Keyword(s):  
Protein Phosphorylation ◽  
Cyclic Nucleotides ◽  
Brain Protein

ACTH-induced inhibition of endogenous rat brain protein phosphorylation in vitro: Structure activity

1978 ◽  
Vol 3 (4) ◽  
pp. 455-463 ◽  
Author(s):  
Henk Zwiers ◽  
Victor Marius Wiegant ◽  
Peter Schotman ◽  
Willem Hendrik Gispen
Keyword(s):  
Protein Phosphorylation ◽  
Rat Brain ◽  
Brain Protein ◽  
Structure Activity

Human brain protein phosphorylation in vitro: Cyclic AMP stimulation of electrophoretically-separated substrates

1981 ◽  
Vol 222 (2) ◽  
pp. 323-333 ◽  
Author(s):  
Aryeh Routtenberg ◽  
David G. Morgan ◽  
Richard G. Conway ◽  
Michael J. Schmidt ◽  
Bernardino Ghetti
Keyword(s):  
Cyclic Amp ◽  
Human Brain ◽  
Protein Phosphorylation ◽  
Brain Protein ◽  
Stimulation Of

Structural requirements for enhancement of T-cell responsiveness by the lymphocyte-specific tyrosine protein kinase p56lck

1992 ◽  
Vol 12 (6) ◽  
pp. 2720-2729
Author(s):  
L Caron ◽  
N Abraham ◽  
T Pawson ◽  
A Veillette
Keyword(s):  
T Cell ◽  
Protein Phosphorylation ◽  
Phospholipase C ◽  
Interleukin 2 ◽  
Cell Receptor ◽  
Amino Terminal ◽  
Src Homology ◽  
Phospholipase C Gamma ◽  
Domain 3

To understand the mechanism(s) by which p56lck participates in T-cell receptor (TCR) signalling, we have examined the effects of mutations in known regulatory domains of p56lck on the ability of F505 p56lck to enhance the responsiveness of an antigen-specific murine T-cell hybridoma. A mutation of the amino-terminal site of myristylation (glycine 2), which prevents stable association of p56lck with the plasma membrane, completely abolished the ability of F505 p56lck to enhance TCR-induced tyrosine protein phosphorylation. Alteration of the major site of in vitro autophosphorylation, tyrosine 394, to phenylalanine diminished the enhancement of TCR-induced tyrosine protein phosphorylation by F505 p56lck. Such a finding is consistent with the previous demonstration that this site is required for full activation of p56lck by mutation of tyrosine 505. Strikingly, deletion of the noncatalytic Src homology domain 2, but not of the Src homology domain 3, markedly reduced the improvement of TCR-induced tyrosine protein phosphorylation by F505 Lck. Additional studies revealed that all the mutations tested, including deletion of the Src homology 3 region, abrogated the enhancement of antigen-triggered interleukin-2 production by F505 p56lck, thus implying more stringent requirements for augmentation of antigen responsiveness by F505 Lck. Finally, it was also observed that expression of F505 p56lck greatly increased TCR-induced tyrosine phosphorylation of phospholipase C-gamma 1, raising the possibility that phospholipase C-gamma 1 may be a substrate for p56lck in T lymphocytes. Our results indicate that p56lck regulates T-cell antigen receptor signalling through a complex process requiring multiple distinct structural domains of the protein.

Calcium regulates motility and protein phosphorylation by changing cAMP and ATP concentrations in boar sperm in vitro

2016 ◽  
Vol 172 ◽  
pp. 39-51 ◽  
Author(s):  
Xinhong Li ◽  
Lirui Wang ◽  
Yuhua Li ◽  
Na Zhao ◽  
Linqing Zhen ◽  
...  
Keyword(s):  
Protein Phosphorylation ◽  
Boar Sperm

scholarly journals Use of Zinc Ions To Study Thylakoid Protein Phosphorylation and the State 1-State 2 Transition In Vitro

1984 ◽  
Vol 74 (2) ◽  
pp. 348-354 ◽  
Author(s):  
John P. Markwell ◽  
Neil R. Baker ◽  
Michael Bradbury ◽  
J. Philip Thornber
Keyword(s):  
Protein Phosphorylation ◽  
The State ◽  
Zinc Ions ◽  
Thylakoid Protein ◽  
State 1 ◽  
Thylakoid Protein Phosphorylation
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