Enzyme adaptation to inhibitor binding: a cryptic binding site in phenylethanolamine N-methyltransferase

Christine L Gee, Nyssa Drinkwater, Joel D A Tyndall, Gary L Grunewald, Qian Wu, Michael J McLeish, Jennifer L Martin

Research output: Contribution to journalArticleResearchpeer-review

21 Citations (Scopus)


Shape complementarity is a fundamental principle of inhibitor design. Here we show that an enzyme for which the crystal structure has been determined (phenylethanolamine N-methyltransferase, PNMT) conceals a cryptic binding site. This site is revealed upon binding of inhibitors that are double the size of the physiological substrate. These large inhibitors are not predicted to bind in that they protrude through the accessible surface calculated from a PNMT/7-aminosulfonyl-1,2,3,4-tetrahydroisoquinoline (SK F 29661) crystal structure, yet they are potent inhibitors of PNMT. We determined structures of the enzyme complexed with large inhibitors and found that the volume of the active site increases by 140 A3 upon binding. Changes in active site size and shape are brought about by unfavorable side chain conformations and rigid body helix motions. The energetic cost is modest, estimated at 2-3 kcal/mol from mutational analyses. Our findings further underline the importance of protein flexibility in structure-based inhibitor design studies.
Original languageEnglish
Pages (from-to)4845 - 4853
Number of pages9
JournalJournal of Medicinal Chemistry
Issue number20
Publication statusPublished - 2007
Externally publishedYes

Cite this