Elasticity of Single Biopolymers Heev L. Ayade A cell constitutes different types of biopolymers that form a complex network. These constituent biopolymers provide mechanical support in maintaining the cell’s shape and facilitate molecular transport within the intracellular environment. Each type of biopolymer in a cell plays an important role in biological functions due to its unique elastic properties. The interplay of these intracellular biopolymers contributes to the cellular dynamics that affect biological function. Therefore, understanding the physics behind the adaptive elasticity of a biopolymer is crucial in gaining biological insights on emergent cellular behavior. The elastic properties of biopolymers have been investigated by stretching the biopolymers using different experimental techniques such as hydrodynamic drag [1], glass needles [2], magnetic tweezers [3], atomic force microscopy [4], magneto-optical tweezers [5], and optical tweezers [6]. The wormlike chain and freely jointed chain models [7] are the common elasticity models used in curve fitting through the experimental force-extension data. The two models use the persistence length, which is employed to describe the elasticity of the biopolymer, and is extracted from the two models after curve fitting. However, the two models set a certain limitation; they cannot fit a broader range of forces in the force-extension data [8]. Therefore, a newly derived elasticity model is used in investigating the elastic properties of biopolymers under tensile stress. The novel elastic model was shown to predict the behavior of stretched biopolymers in a broader range of forces, in contrast to the wormlike chain and freely jointed chain models. Our approach is generically applicable to biopolymers and is applicable to other polymer types of similar properties. F F L Figure: The stretching of a biopolymer. One end of a biopolymer could be clamped using a micropipette. L References 1. T.T. Perkins, D.E. Smith, R.G. Larson, and S. Chu, “Stretching of a Single Tethered Polymer in a Uniform Flow,” Science 268, 83-87 (1995). 2. J.F. Leger, G. Romano, A. Sarkar, J. Robert, L. Bourdieu, D. Chatenay and J.F. Marko, “Structural Transitions of a Twisted and Stretched DNA Molecule,” Phys. Rev. Lett. 83, 5 (1999). 3. T. Strick, J-F. Allemand, V. Croquette, and D. Bensimon, “Twisting and Stretching Single DNA Molecules,” Progress in Biophysics & Molecular Biology 74, 115-140 (2000). 4. P.A. Wiggins, T. van der Heijden, F. Moreno-Herrero, A. Spakowitz, R. Phillips, J. Widom, C. Dekker, and P.C. Nelson, “High Flexibility of DNA on Short Length Scales Probed by Atomic Force Microscopy,” Nature Nanotechnology 1, 137-141 (2006). 5. A. Crut, D.A. Koster, R. Seidel, C.H. Wiggins, and N.H. Dekker, “Fast dynamics of supercoiled DNA revealed by single-molecule experiments,” Proc. Natl. Acad. Sci. USA 104, 11957-11962 (2007). 6. Y.-L. Sun, Z.-P. Luo, and K.-N. An, “Stretching Short Biopolymers Using Optical Tweezers,” Biochemical and Biophysical Research Communications 286, 826–830 (2001). 7. C. Bustamante, J.F. Marko, and E.D. Siggia, “Entropic elasticity of λ-phage DNA,” Science 265, 1599-1600 (1994). C. Storm and P. C. Nelson, “Theory of high-force DNA stretching and overstretching,” Physical Review E 67, 051906 (2003).