New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin
A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit f...
Ausführliche Beschreibung
Autor*in: |
Yoo, Soyeon [verfasserIn] Han, Min Su [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Dyes and pigments - Amsterdam [u.a.] : Elsevier Science, 1980, 196 |
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Übergeordnetes Werk: |
volume:196 |
DOI / URN: |
10.1016/j.dyepig.2021.109804 |
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Katalog-ID: |
ELV006726194 |
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245 | 1 | 0 | |a New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin |
264 | 1 | |c 2021 | |
336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
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520 | |a A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. | ||
650 | 4 | |a Mono- and dipeptidyl-carboxypeptidase | |
650 | 4 | |a Fluorescent substrates | |
650 | 4 | |a Angiotensin-converting enzyme | |
650 | 4 | |a Carboxypeptidase B | |
650 | 4 | |a Signal amplification | |
650 | 4 | |a Albumin | |
700 | 1 | |a Han, Min Su |e verfasserin |0 (orcid)0000-0001-9588-6980 |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Dyes and pigments |d Amsterdam [u.a.] : Elsevier Science, 1980 |g 196 |h Online-Ressource |w (DE-627)306658755 |w (DE-600)1500382-6 |w (DE-576)116550910 |x 0143-7208 |7 nnns |
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912 | |a GBV_ILN_100 | ||
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912 | |a GBV_ILN_110 | ||
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912 | |a GBV_ILN_224 | ||
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912 | |a GBV_ILN_602 | ||
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912 | |a GBV_ILN_2034 | ||
912 | |a GBV_ILN_2038 | ||
912 | |a GBV_ILN_2044 | ||
912 | |a GBV_ILN_2048 | ||
912 | |a GBV_ILN_2049 | ||
912 | |a GBV_ILN_2050 | ||
912 | |a GBV_ILN_2056 | ||
912 | |a GBV_ILN_2059 | ||
912 | |a GBV_ILN_2061 | ||
912 | |a GBV_ILN_2064 | ||
912 | |a GBV_ILN_2065 | ||
912 | |a GBV_ILN_2068 | ||
912 | |a GBV_ILN_2088 | ||
912 | |a GBV_ILN_2111 | ||
912 | |a GBV_ILN_2112 | ||
912 | |a GBV_ILN_2113 | ||
912 | |a GBV_ILN_2118 | ||
912 | |a GBV_ILN_2122 | ||
912 | |a GBV_ILN_2129 | ||
912 | |a GBV_ILN_2143 | ||
912 | |a GBV_ILN_2147 | ||
912 | |a GBV_ILN_2148 | ||
912 | |a GBV_ILN_2152 | ||
912 | |a GBV_ILN_2153 | ||
912 | |a GBV_ILN_2190 | ||
912 | |a GBV_ILN_2336 | ||
912 | |a GBV_ILN_2470 | ||
912 | |a GBV_ILN_2507 | ||
912 | |a GBV_ILN_2522 | ||
912 | |a GBV_ILN_4035 | ||
912 | |a GBV_ILN_4037 | ||
912 | |a GBV_ILN_4046 | ||
912 | |a GBV_ILN_4112 | ||
912 | |a GBV_ILN_4125 | ||
912 | |a GBV_ILN_4126 | ||
912 | |a GBV_ILN_4242 | ||
912 | |a GBV_ILN_4251 | ||
912 | |a GBV_ILN_4305 | ||
912 | |a GBV_ILN_4313 | ||
912 | |a GBV_ILN_4322 | ||
912 | |a GBV_ILN_4323 | ||
912 | |a GBV_ILN_4324 | ||
912 | |a GBV_ILN_4326 | ||
912 | |a GBV_ILN_4333 | ||
912 | |a GBV_ILN_4334 | ||
912 | |a GBV_ILN_4335 | ||
912 | |a GBV_ILN_4338 | ||
912 | |a GBV_ILN_4393 | ||
936 | b | k | |a 58.26 |j Technologie der Farben und Lacke |
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58.26 |
publishDate |
2021 |
allfields |
10.1016/j.dyepig.2021.109804 doi (DE-627)ELV006726194 (ELSEVIER)S0143-7208(21)00670-7 DE-627 ger DE-627 rda eng 660 DE-600 58.26 bkl Yoo, Soyeon verfasserin aut New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. Mono- and dipeptidyl-carboxypeptidase Fluorescent substrates Angiotensin-converting enzyme Carboxypeptidase B Signal amplification Albumin Han, Min Su verfasserin (orcid)0000-0001-9588-6980 aut Enthalten in Dyes and pigments Amsterdam [u.a.] : Elsevier Science, 1980 196 Online-Ressource (DE-627)306658755 (DE-600)1500382-6 (DE-576)116550910 0143-7208 nnns volume:196 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 58.26 Technologie der Farben und Lacke AR 196 |
spelling |
10.1016/j.dyepig.2021.109804 doi (DE-627)ELV006726194 (ELSEVIER)S0143-7208(21)00670-7 DE-627 ger DE-627 rda eng 660 DE-600 58.26 bkl Yoo, Soyeon verfasserin aut New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. Mono- and dipeptidyl-carboxypeptidase Fluorescent substrates Angiotensin-converting enzyme Carboxypeptidase B Signal amplification Albumin Han, Min Su verfasserin (orcid)0000-0001-9588-6980 aut Enthalten in Dyes and pigments Amsterdam [u.a.] : Elsevier Science, 1980 196 Online-Ressource (DE-627)306658755 (DE-600)1500382-6 (DE-576)116550910 0143-7208 nnns volume:196 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 58.26 Technologie der Farben und Lacke AR 196 |
allfields_unstemmed |
10.1016/j.dyepig.2021.109804 doi (DE-627)ELV006726194 (ELSEVIER)S0143-7208(21)00670-7 DE-627 ger DE-627 rda eng 660 DE-600 58.26 bkl Yoo, Soyeon verfasserin aut New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. Mono- and dipeptidyl-carboxypeptidase Fluorescent substrates Angiotensin-converting enzyme Carboxypeptidase B Signal amplification Albumin Han, Min Su verfasserin (orcid)0000-0001-9588-6980 aut Enthalten in Dyes and pigments Amsterdam [u.a.] : Elsevier Science, 1980 196 Online-Ressource (DE-627)306658755 (DE-600)1500382-6 (DE-576)116550910 0143-7208 nnns volume:196 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 58.26 Technologie der Farben und Lacke AR 196 |
allfieldsGer |
10.1016/j.dyepig.2021.109804 doi (DE-627)ELV006726194 (ELSEVIER)S0143-7208(21)00670-7 DE-627 ger DE-627 rda eng 660 DE-600 58.26 bkl Yoo, Soyeon verfasserin aut New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. Mono- and dipeptidyl-carboxypeptidase Fluorescent substrates Angiotensin-converting enzyme Carboxypeptidase B Signal amplification Albumin Han, Min Su verfasserin (orcid)0000-0001-9588-6980 aut Enthalten in Dyes and pigments Amsterdam [u.a.] : Elsevier Science, 1980 196 Online-Ressource (DE-627)306658755 (DE-600)1500382-6 (DE-576)116550910 0143-7208 nnns volume:196 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 58.26 Technologie der Farben und Lacke AR 196 |
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10.1016/j.dyepig.2021.109804 doi (DE-627)ELV006726194 (ELSEVIER)S0143-7208(21)00670-7 DE-627 ger DE-627 rda eng 660 DE-600 58.26 bkl Yoo, Soyeon verfasserin aut New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. Mono- and dipeptidyl-carboxypeptidase Fluorescent substrates Angiotensin-converting enzyme Carboxypeptidase B Signal amplification Albumin Han, Min Su verfasserin (orcid)0000-0001-9588-6980 aut Enthalten in Dyes and pigments Amsterdam [u.a.] : Elsevier Science, 1980 196 Online-Ressource (DE-627)306658755 (DE-600)1500382-6 (DE-576)116550910 0143-7208 nnns volume:196 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 58.26 Technologie der Farben und Lacke AR 196 |
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New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin |
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Yoo, Soyeon |
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Yoo, Soyeon Han, Min Su |
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title_sort |
new strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin |
title_auth |
New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin |
abstract |
A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. |
abstractGer |
A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. |
abstract_unstemmed |
A new strategy to design a fluorescent substrate for carboxypeptidases (CPs) was devised using dansylated sarcosine (DS) and albumin as a fluorophore and signal amplifier, respectively. The fluorescent substrate was designed by attaching an amino acid or peptide, which acts as the recognition unit for CP, to the C-terminus of DS. In the presence of the target CP, the low-fluorescence substrate is hydrolyzed to a strongly fluorescent DS by binding with albumin. As a proof concept, Dansyl-Sar-Lys-Pro (DS-KP) and Dansyl-Sar-Arg (DS-R) were developed as fluorescent substrates for the angiotensin-converting enzyme and carboxypeptidase B, respectively. The CP assay system was verified to be capable of measuring the activities of both dipeptidyl-CP and mono-CP and the inhibition efficiency of various CP inhibitors, confirming its applicability as a high-throughput screening method for numerous inhibitor candidates. |
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title_short |
New strategy to design fluorescent substrates of carboxypeptidases using a combination of dansylated peptides and albumin |
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up_date |
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