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Small-angle X-ray and neutron scattering data were used to study the solution structure of calmodulin complexed with a synthetic peptide corresponding to residues 577-603 of rabbit skeletal muscle myosin light chain kinase. The X-ray data indicate that, in the presence of Ca2+, the calmodulin-peptide complex has a structure that is considerably more compact than uncomplexed calmodulin. The radius of gyration, Rg, for the complex is approximately 20% smaller than that of uncomplexed Ca2+.calmodulin (16 vs 21 A), and the maximum dimension, dmax, for the complex is also about 20% smaller (49 vs 67 A). The peptide-induced conformational rearrangement of calmodulin is [Ca2+] dependent. The length distribution function for the complex is more symmetric than that for uncomplexed Ca2+.calmodulin, indicating that more of the mass is distributed toward the center of mass for the complex, compared with the dumbell-shaped Ca2+.calmodulin. The solvent contrast dependence of Rg for neutron scattering indicates that the peptide is located more toward the center of the complex, while the calmodulin is located more peripherally, and that the centers of mass of the calmodulin and the peptide are not coincident. The scattering data support the hypothesis that the interconnecting helix region observed in the crystal structure for calmodulin is quite flexible in solution, allowing the two lobes of calmodulin to form close contacts on binding the peptide. This flexibility of the central helix may play a critical role in activating target enzymes such as myosin light chain kinase.

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Small-angle X-ray and neutron scattering have been used to study the solution structures of calmodulin complexed with synthetic peptides corresponding to residues 342-366 and 301-326, designated PhK5 and PhK13, respectively, in the regulatory domain of the catalytic subunit of skeletal muscle phosphorylase kinase. The scattering data show that binding of PhK5 to calmodulin induces a dramatic contraction of calmodulin, similar to that previously observed when calmodulin is complexed with the calmodulin-binding domain peptide from rabbit skeletal muscle myosin light chain kinase. In contrast, calmodulin remains extended upon binding PhK13. In the presence of both peptides, calmodulin also remains extended. Apparently, the presence of PhK13 inhibits calmodulin from undergoing the PhK5-induced contraction. These data indicate that there is a fundamentally different type of calmodulin-target enzyme interaction in the case of the catalytic subunit of phosphorylase kinase compared with that for myosin light chain kinase.

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The importance of small‐angle neutron scattering (SANS) in biological, chemical, physical and engineering research mandates that all intense neutron sources be equipped with SANS instruments. Four existing instruments at pulsed sources are described and the general differences between pulsed‐source and reactor‐based instrument designs are discussed. The basic geometries are identical, but dynamic range is generally achieved by using a broad band of wavelengths (with time‐of‐flight analysis) rather than by moving the detector. This allows optimization for maximum beam intensity at a given beam size over the full dynamic range with fixed collimation. Data‐acquisition requirements at a pulsed source are more severe, requiring large fast histograming memories. Data reduction is also more complex, as all wavelength‐dependent and angle‐dependent backgrounds and nonlinearities must be accounted for before data can be transformed to intensity versus momentum transfer (Q). A comparison is shown between the Los Alamos pulsed instrument and DII (Institut Laue–Langevin) and examples from the four major topics of the conference are shown. The general conclusion is that reactor‐based instruments remain superior at very low Q or if only a narrow range of Q is required, but that the current generation of pulsed‐source instruments is competitive at moderate Q and may be faster when a wide range of Q is required.