Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography

Dissing, J. ; Dahl, O. ; Svensmark, O.

Amsterdam : Elsevier
ISSN:
0005-2744
Keywords:
(Affinity chromatography) ; Acid phosphatase inhibitor ; Arsonic acid ; Phosphonic acid
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Biology
Type of Medium:
Electronic Resource
URL:
_version_ 1798292371117441024
autor Dissing, J.
Dahl, O.
Svensmark, O.
autorsonst Dissing, J.
Dahl, O.
Svensmark, O.
book_url http://linkinghub.elsevier.com/retrieve/pii/0005-2744(79)90051-2
datenlieferant nat_lic_papers
fussnote 1.|In order to obtain an effective ligand for affinity chromatography of the low molecular weight acid phosphatase (orthophosphoric-monoester phosphohydrolase (acid optimum), EC 3.1.3.2) from human red cells nine phosphonic and two arsinic acid substrate analogues were investigated as potential inhibitors. The two forms of acid phosphatase type B (b"1 and b"2) were isolated and partially purified using conventional methods and the inhibitory action of the substrate analogs investigated.2.|Four of the phosphonic acids were relatively effective competitive inhibitors. It appears that certain structural and electronic requirements have to be fulfilled by the phosphonic acid in order to exhibit significant affinity for the enzyme. A high affinity appears to require the presence of a bulky, hydrophobic moiety which has to be separated from the phosphorus atom by the distance of one atom.3.|p-Aminobenzylphosphonic acid exerted the highest affinity for acid phosphatase with a pH optimum at 6.5. K"i values of 4 . 10^-^4 and 6 . 10^-^4 M were found for the b"1 and b"2 forms, respectively.4.|Coupling of p-aminobenzylphosphonic acid to Agarose yielded an effective and specific affinity medium. By means of affinity chromatography using this medium, acid phosphatase was purified 500-fold in a single step.
hauptsatz hsatz_simple
identnr NLZ185763960
issn 0005-2744
journal_name BBA - Enzymology
materialart 1
package_name Elsevier
publikationsort Amsterdam
publisher Elsevier
reference 569 (1979), S. 159-176
schlagwort (Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
search_space articles
shingle_author_1 Dissing, J.
Dahl, O.
Svensmark, O.
shingle_author_2 Dissing, J.
Dahl, O.
Svensmark, O.
shingle_author_3 Dissing, J.
Dahl, O.
Svensmark, O.
shingle_author_4 Dissing, J.
Dahl, O.
Svensmark, O.
shingle_catch_all_1 Dissing, J.
Dahl, O.
Svensmark, O.
Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
0005-2744
00052744
Elsevier
shingle_catch_all_2 Dissing, J.
Dahl, O.
Svensmark, O.
Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
0005-2744
00052744
Elsevier
shingle_catch_all_3 Dissing, J.
Dahl, O.
Svensmark, O.
Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
0005-2744
00052744
Elsevier
shingle_catch_all_4 Dissing, J.
Dahl, O.
Svensmark, O.
Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
(Affinity chromatography)
Acid phosphatase inhibitor
Arsonic acid
Phosphonic acid
0005-2744
00052744
Elsevier
shingle_title_1 Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
shingle_title_2 Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
shingle_title_3 Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
shingle_title_4 Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
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wilbert
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source_archive Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
timestamp 2024-05-06T08:47:25.843Z
titel Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
titel_suche Phosphonic and arsonic acids as inhibitors of human red cell acid phosphatase and their use in affinity chromatography
1.|In order to obtain an effective ligand for affinity chromatography of the low molecular weight acid phosphatase (orthophosphoric-monoester phosphohydrolase (acid optimum), EC 3.1.3.2) from human red cells nine phosphonic and two arsinic acid substrate analogues were investigated as potential inhibitors. The two forms of acid phosphatase type B (b"1 and b"2) were isolated and partially purified using conventional methods and the inhibitory action of the substrate analogs investigated.2.|Four of the phosphonic acids were relatively effective competitive inhibitors. It appears that certain structural and electronic requirements have to be fulfilled by the phosphonic acid in order to exhibit significant affinity for the enzyme. A high affinity appears to require the presence of a bulky, hydrophobic moiety which has to be separated from the phosphorus atom by the distance of one atom.3.|p-Aminobenzylphosphonic acid exerted the highest affinity for acid phosphatase with a pH optimum at 6.5. K"i values of 4 . 10^-^4 and 6 . 10^-^4 M were found for the b"1 and b"2 forms, respectively.4.|Coupling of p-aminobenzylphosphonic acid to Agarose yielded an effective and specific affinity medium. By means of affinity chromatography using this medium, acid phosphatase was purified 500-fold in a single step.
topic W
uid nat_lic_papers_NLZ185763960