HELIX-FORMING TENDENCIES OF AMINO-ACIDS DEPEND ON THE RESTRICTIONS OF SIDE-CHAIN ROTAMER CONFORMATIONS - CRYSTAL-STRUCTURE OF THE TRIPEPTIDE GAI IN 2 CRYSTALLINE FORMS

In our attempts to design crystalline alpha-helical peptides, we synthesized and crystallized GAI (C11H21N3O4) in two crystal forms, GAI1 and GAI2. Form 1 (GAI1) Gly-L-Ala-L-Ile (C11H21N3O4.3H2O) crystals are monoclinic, space group P2(1) with a = 8.171(2), b = 6.072(4), c = 16.443(4) angstrom, beta = 101.24(2)-degrees, V = 800 angstrom3, D(c) = 1.300 g cm-3 and Z = 2, R = 0.081 for 482 reflections. Form 2 (GAI2) Gly-L-Ala-L-Ile (C11H21N3O4.1/2 H2O) is triclinic, space group P1 with a = 5.830(1), b = 8.832(2), c = 15.008(2) angstrom, alpha = 102.88(1), beta = 101.16(2), gamma = 70.72(2)-degrees, V = 705 angstrom 3, Z = 2, D(c) = 1.264 g cm-3, R = 0.04 for 2582 reflections. GAI1 is isomorphous with GAV and forms a helix, whereas GAI2 does not. In GAI1, the tripeptide molecule is held in a near helical conformation by a water molecule that bridges the NH3+ and COO- groups, and acts as the fourth residue needed to complete the turn by forming two hydrogen bonds. Two other water molecules form intermolecular hydrogen bonds in stabilizing the helical structure so that the end result is a column of molecules that looks like an incipient alpha-helix. GAI2 imitates a cyclic peptide and traps a water molecule. The conformation angles chi-11 and chi-12 for the side chain are (-63.7-degrees, 171.1-degrees) for the helical GAI1, and (-65.1-degrees, 58.6-degrees) and (-65.0-degrees, 58.9-degrees) for the two independent nonhelical molecules in GAI2; in GAI1, both the C(gamma) atoms point away from the helix, whereas in GAI2 the C(gamma) atom with the g+ conformation points inward to the helix and causes sterical interaction with atoms in the adjacent peptide plane. From these results, it is clear that the helix-forming tendencies of amino acids correlate with the restrictions of side-chain rotamer conformations. Both the peptide units in GAI1 are trans and show significant deviation from planarity [omega-1 = -168(1)-degrees; omega-2 = -171(1)-degrees] whereas both the peptide units in both the molecules A and B in GAI2 do not show significant deviation from planarity [omega-1 = 179.3(3)-degrees; omega-2 = -179.3(3)-degrees for molecule A and omega-1 = 179.5(3)-degrees; omega-2 = -179.4(3)-degrees for molecule B], indicating that the peptide planes in these incipient alpha-helical peptides are considerably bent.