Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs
We present here the calculation of the mean time to capture of a tethered ligand to the receptor. This calculation is then used to determine the shift in the partitioning between (1) free, (2) singly bound, and (3) doubly bound ligands in chemical equilibrium as a function of the length of the tethe...
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2016-09-01
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doaj-ac51377005434eb5bb2b465a79376fe72020-11-25T00:09:21ZengElsevierData in Brief2352-34092016-09-018506515Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairsLu Shen0Caitlin G. Decker1Heather D. Maynard2Alex J. Levine3Department of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095, USADepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095, USADepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095, USA; California Nanosystems Institute, University of California, Los Angeles, CA 90095, USADepartment of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095, USA; Department of Physics & Astronomy, University of California, Los Angeles, CA 90095, USA; Department of Biomathematics, University of California, Los Angeles, CA 90095, USA; California Nanosystems Institute, University of California, Los Angeles, CA 90095, USA; Corresponding author at: Department of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095, USA.We present here the calculation of the mean time to capture of a tethered ligand to the receptor. This calculation is then used to determine the shift in the partitioning between (1) free, (2) singly bound, and (3) doubly bound ligands in chemical equilibrium as a function of the length of the tether. These calculations are used in the research article Fibroblast Growth Factor 2 Dimer with Superagonist in vitro Activity Improves Granulation Tissue Formation During Wound Healing (Decker et al., in press [1]) to explain quantitatively how changes in polymeric linker length in the ligand dimers modifies the efficacy of these molecules relative to that of free ligands. Keywords: Ligand bindinghttp://www.sciencedirect.com/science/article/pii/S2352340916303389 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lu Shen Caitlin G. Decker Heather D. Maynard Alex J. Levine |
spellingShingle |
Lu Shen Caitlin G. Decker Heather D. Maynard Alex J. Levine Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs Data in Brief |
author_facet |
Lu Shen Caitlin G. Decker Heather D. Maynard Alex J. Levine |
author_sort |
Lu Shen |
title |
Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs |
title_short |
Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs |
title_full |
Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs |
title_fullStr |
Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs |
title_full_unstemmed |
Calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs |
title_sort |
calculating the mean time to capture for tethered ligands and its effect on the chemical equilibrium of bound ligand pairs |
publisher |
Elsevier |
series |
Data in Brief |
issn |
2352-3409 |
publishDate |
2016-09-01 |
description |
We present here the calculation of the mean time to capture of a tethered ligand to the receptor. This calculation is then used to determine the shift in the partitioning between (1) free, (2) singly bound, and (3) doubly bound ligands in chemical equilibrium as a function of the length of the tether. These calculations are used in the research article Fibroblast Growth Factor 2 Dimer with Superagonist in vitro Activity Improves Granulation Tissue Formation During Wound Healing (Decker et al., in press [1]) to explain quantitatively how changes in polymeric linker length in the ligand dimers modifies the efficacy of these molecules relative to that of free ligands. Keywords: Ligand binding |
url |
http://www.sciencedirect.com/science/article/pii/S2352340916303389 |
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