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Details of SAPdb entry with Sequence YS
Primary information
SAPdb ID 1360,
PMID24256076
Peptide NameYS
Peptide sequenceYS
N-Terminal ModificationFmoc [or N-(fluorenyl-9-methoxycarbonyl)]
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueAFM (Atomic Force Microscopy, Fluorescence Emission Spectroscopy and DLS (Dynamic Light Scattering)
Solvent100mM Phosphate buffer
Methodself-assembly of peptides is induced by sonicating and vortexing the Fmoc-dipeptides (10 mM) in 100 mM sodium phosphate buffer (pH 8) solution with (or without) the addition of various concentrations of proteins β- lactoglobulin (β-LG) and Bovine serum albumin (BSA) in the range of 0.03 to 0.2 wt %.
Conc10mM
Temperature8
TemperatureRoom temperature
Incubation Time2 hours
Year2013
Self assemblyYes
Type of Self assemblyHydogel (consists of Nanofibers)
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
NA
Hydrogel
195
YS
N.A.
Primary information
SAPdb ID 1363,
PMID24256076
Peptide NameYS
Peptide sequenceYS
N-Terminal ModificationFmoc [or N-(fluorenyl-9-methoxycarbonyl)]
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueAFM (Atomic Force Microscopy, Fluorescence Emission Spectroscopy and DLS (Dynamic Light Scattering)
Solvent100mM Phosphate buffer
Methodself-assembly of peptides is induced by sonicating and vortexing the Fmoc-dipeptides (10 mM) in 100 mM sodium phosphate buffer (pH 8) solution with (or without) the addition of various concentrations of proteins β- lactoglobulin (β-LG) and Bovine serum albumin (BSA) in the range of 0.03 to 0.2 wt %.
Conc10mM
Temperature8
TemperatureRoom temperature
Incubation Time3 - 6 hours
Year2013
Self assemblyYes
Type of Self assemblyHydogel (consists of Nanofibers)
Tertiary Structure
(Technique)
Not Predicted),
Linear
in presence of 0.2 % β-LG
NA
Hydrogel
82.5
YS
N.A.
Primary information
SAPdb ID 1366,
PMID24256076
Peptide NameYS
Peptide sequenceYS
N-Terminal ModificationFmoc [or N-(fluorenyl-9-methoxycarbonyl)]
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueAFM (Atomic Force Microscopy, Fluorescence Emission Spectroscopy and DLS (Dynamic Light Scattering)
Solvent100mM Phosphate buffer
Methodself-assembly of peptides is induced by sonicating and vortexing the Fmoc-dipeptides (10 mM) in 100 mM sodium phosphate buffer (pH 8) solution with (or without) the addition of various concentrations of proteins β- lactoglobulin (β-LG) and Bovine serum albumin (BSA) in the range of 0.03 to 0.2 wt %.
Conc10mM
Temperature8
TemperatureRoom temperature
Incubation Time3 - 6 hours
Year2013
Self assemblyYes
Type of Self assemblyHydogel (consists of Nanofibers)
Tertiary Structure
(Technique)
Not Predicted),
Linear
in presence of 0.2 % BSA
NA
Hydrogel
195
YS
N.A.
Primary information
SAPdb ID 1623,
PMID24896538
Peptide NameFmoc-YS
Peptide sequenceYS
N-Terminal ModificationFmoc [or N-(fluorenyl-9-methoxycarbonyl)]
C-Terminal ModificationFree
Non-Terminal ModificationNone
Length2
Peptide/ConjuagatePeptide
Conjugate partnerNone
TechniqueScanning Electron Microscopy (SEM) and AFM (Atomic force Microscopy)
SolventPhosphate buffer
Method10 mM Fmoc-YS solution was prepared by dissolving 5.32 mg of Fmoc-YS in 1 mL of phosphate buffer solution. Emulsion formed after hand-shaking for 5 s emulsions form in vials. Gel formed in 24 hours on incubation at room temperature.
Conc10mM
Temperature8
TemperatureRoom temperature
Incubation Time24 hours
Year2014
Self assemblyYes
Type of Self assemblyGel (consist of Fibrous network)
Tertiary Structure
(Technique)
Not Predicted),
Linear
NA
NA
Hydrogel
NA
YS
N.A.