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PMID: 163643 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Simple alkanethiol groups for temporary blocking of sulfhydryl groups of enzymes.

Biochemistry ·Vol. 14 ·No. 4 ·1975-02-25 ·Pages 766-71

Smith DJ, Maggio ET, Kenyon GL

Abstract

New reagents for the temporary blocking of active or accessible sulfhydryl groups of enzymes have been developed. These reagents, which are either alkyl alkanethiolsulfonates or alkoxycarbonylalkyl disulfides, rapidly and quantitatively place various RS- groups on the sulfhydryls to generate mixed disulfides. In all cases native enzymes can be regenerated with either dithiothreitol or beta-mercaptoethanol. In general the temporary blocking groups also afford total protection against normally inhibitory thiol blocking agents. When RS- groups were attached to rabbit muscle creatine kinase (EC 2.7.3.2), a trend toward lower residual activities with increasing bulk was observed. Treatment of the native creatine kinase with 14CH3HgC1 led to incorporation of greater than 1 equiv of CH3Hg- group per subunit. This CH3Hg- blocked enzyme was fully active, and the blocking group afforded no protection against iodoacetamide. These results suggest that CH3Hg- and the RS- groups are modifying two different sulhydryl groups on the enzyme. When papain (EC 3.4.4.10) was treated with excess methyl methanethiolsulfonate. complete and rapid inhibition was observed, and 1 equiv of CH3S- was incorporated/mol of active enzyme. Complete protection against normally inhibitory 5,5'-dithiobis(2-nitrobenzoic acid) was afforded by the temporary blocking group. When rabbit muscle glyceraldehyde-3-phosphate dehydrogenase (EC 1.2.1.12) was titrated with methyl methanethiolsulfonate, two sulfhydryl groups per subunit were found to be modified, one much more rapidly than the other. If one extrapolates the initial slope of the titration curve, the inactivation of the enzyme would be complete after modification of a single cysteinyl residue per subunit.

MeSH Terms
Alkanes/pharmacology Animals Benzoates/pharmacology Binding Sites Creatine Kinase/antagonists & inhibitors Glyceraldehyde-3-Phosphate Dehydrogenases/antagonists & inhibitors Kinetics Mesylates/pharmacology Muscles/enzymology Nitro Compounds/pharmacology Papain/antagonists & inhibitors Protein Binding Rabbits Sulfhydryl Reagents/pharmacology
Chemicals
Alkanes Benzoates Mesylates Nitro Compounds Sulfhydryl Reagents Glyceraldehyde-3-Phosphate Dehydrogenases Creatine Kinase Papain
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Smith D J
Maggio E T
Kenyon G L
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1975-02-25
Pages
766-71
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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