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dc.contributor.authorMARTIN, JL
dc.contributor.authorVELURAJA, K
dc.contributor.authorROSS, K
dc.contributor.authorJOHNSON, LN
dc.contributor.authorFLEET, GWJ
dc.contributor.authorRAMSDEN, NG
dc.contributor.authorBRUCE, I
dc.contributor.authorORCHARD, MG
dc.contributor.authorOIKONOMAKOS, NG
dc.contributor.authorPAPAGEORGIOU, AC
dc.contributor.authorLEONIDAS, DD
dc.contributor.authorTSITOURA, HS
dc.date.accessioned2018-07-18T03:26:34Z
dc.date.available2018-07-18T03:26:34Z
dc.date.issued1991
dc.identifier.issn0006-2960
dc.identifier.doi10.1021/bi00106a006
dc.identifier.urihttp://hdl.handle.net/10072/378685
dc.description.abstractabstract: The T-state crystal structure of the glucose-phosphorylase b complex has been used as a model for the design of glucose analogue inhibitors that may be effective in the regulation of blood glucose levels. Modeling studies indicated room for additional atoms attached at the C1-/3 position of glucose and some scope for additional atoms at the Cl-a position. Kinetic parameters were determined for a-D-glucose: K{ = 1.7 mM, Hill coefficient n = 1.5, and a (synergism with caffeine) = 0.2. For /3-D-glucose, K{ = 1A mM, n = 1.5, and a = 0.4. More than 20 glucose analogues have been synthesized and tested in kinetic experiments. Most were less effective inhibitors than glucose itself and the best inhibitor was a-hydroxymethyl-1- deoxy-D-glucose (Kt = 1.5 mM, n = 1.3, a = 0.4). The binding of 14 glucose analogues to glycogen phosphorylase b in the crystal has been studied at 2.4-A resolution and the structure have been refined to crystallographic R values of less than 0.20. The kinetic and crystallographic studies have been combined to provide rationalizations for the apparent affinities of glucose and the analogues. The results show the discrimination against /3-D-glucose in favor of a-D-glucose is achieved by an additional hydrogen bond made in the a-glucose complex through water to a protein group and an unfavorable environment for a polar group in the /3 pocket. The compound a-hydroxymethyl-l-deoxy-D-glucose has an affinity similar to that of glucose and makes a direct hydrogen bond to a protein group. Comparison of analogues with substituent atoms that have flexible geometry (e.g., 1-hydroxyethyl /3-D-glucoside) with those whose substituent atoms are more rigid (e.g., /3-azidomethyl-1 -deoxyglucose or /3-cyanomethyl-1 -deoxyglucose) indicates that although all three compounds make similar polar interactions with the enzyme, those with more rigid substituent groups are better inhibitors. In another example, a-azidomethyl-1 -deoxyglucose was a poor inhibitor. In the crystal structure the compound made several favorable interactions with the enzyme but bound in an unfavorable conformation, thus providing an explanation for its poor inhibition. Attempts to utilize a contact to a buried aspartate group were partially successful for a number of compounds (/3-aminoethyl, /3-mesylate, and /3-azidomethyl analogues). The /3 pocket was shown to bind gentiobiose (6-0-/3-D-glucopyranosyl-Dglucose), indicating scope for binding of larger side groups for future studies.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofpagefrom10101
dc.relation.ispartofpageto10116
dc.relation.ispartofissue42
dc.relation.ispartofjournalBiochemistry
dc.relation.ispartofvolume30
dc.subject.fieldofresearchBiochemistry and Cell Biology not elsewhere classified
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchBiochemistry and Cell Biology
dc.subject.fieldofresearchMedical Biochemistry and Metabolomics
dc.subject.fieldofresearchcode060199
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0601
dc.subject.fieldofresearchcode1101
dc.titleGlucose analogue inhibitors of glycogen phosphorylase: the design of potential drugs for diabetes
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.hasfulltextNo Full Text
gro.griffith.authorMartin, Jennifer


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