A spin label study of immobilized enzyme spectral subpopulations

Abstract

Electron spin resonance (ESR) spin label studies have been carried out to examine the active site conformation of α‐chymotrypsin before and after immobilization on two types of organic polymer supports: Amberlite XAD‐8 and XAD‐2. α‐Chymotryspin was first chemically modified by reaction with methyl‐4‐phenylbutyrimidate and then inhibited by the active site spin label 4‐(2,2,6,6‐tetramethyl‐piperdine‐1‐oxyl)‐m‐flurosulfonylbenzamide. In general, the ESR spectra of the active site lable revealed no significant changes in conformation for most of the enzyme before or after derivatization. On the other hand, two spectral subpopulations (A and B) of spin‐labeled enzyme were characterized on the basis of their ESR spectra after immobilization on Amberlite XAD‐8. Spectral subpopulation A (distinguished by a highly restrained spectrum) appeared to retain its active site structure and conformation and represented a large majority of the labeled chymotrypsin on the beads. Its presence correlated with the high activity and stability of phenylbutyramidinated chymotryspin on the Amberlite XAD‐8 beads. Spectral subpopulation B (distinguished by a very weakly constrained spectrum) appeared to reflect loosely bound or denatured enzyme which was removable upon washing with 40% (v/v) ethylene glycol. Two methods for examining solvent accessibility to the active site lable of the kinetics of ascorbate reduction suggested that both spectral subpopulations had identical accessibilities to the bulk solvent. Paramagnetic broadening of the signal by K₃Fe(CN)₆ revealed differences in the spin–spin broadening of the A and B components but is deemed and inappropriate indicator of solvent accessibility.