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Mu Gao, Matthias Wilmanns, and Klaus Schulten. Steered molecular dynamics studies of titin I1 domain unfolding. Biophysical Journal, 2002. In press. The cardiac muscle protein titin, responsible for developing passive elasticity and extensibility of muscle, possesses about 40 immunoglobulin-like (Ig) domains in its I band region. Atomic force microscopy and steered molecular dynamics (SMD) have been successfully combined to investigate the reversible unfolding of individual Ig domains. However, previous SMD studies of titin I- band modules have been restricted to I27, the only structurally known Ig domain from the distal region of the titin I-band. In this paper we report SMD simulations unfolding I1, the first structurally available Ig domain from the proximal region of the titin I band. The simulations are carried out with a view towards upcoming atomic force microscopy experiments. Both constant velocity and constant force stretching have been employed to model mechanical unfolding of oxidized I1, which has a disulfide bond bridging $\beta$-strands C and E, as well as reduced I1 in which the disulfide bridge is absent. The simulations reveal that I1 is protected against external stress mainly through six inter-strand hydrogen bonds between its A and B $\beta$-strands. The disulfide bond enhances the mechanical stability of oxidized I1 domains by restricting the rupture of backbone hydrogen bonds between the A'- and G-strands. The disulfide bond also limits the maximum extension of I1 to about 22 nm. Comparison of the unfolding pathways of I1 and I27 are provided and implications to AFM experiments are discussed. Full Text

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