PubMed Health⌕ Search

PubMed · 9174959

Size-exclusion phases and repulsive protein--polymer interaction/recognition.

Abstract

Size-dependent exclusion of macromolecules from gel matrices has long been discussed in terms of pore models. An alternate approach is to calculate the partition coefficient of the distributed species between the matrix material and the mobile phase assuming that the gel can be treated as a polymer solution of appropriate concentration and molecular weight. This approach is particularly appealing in attempting to predict the behaviour of 'tentacle' phases in which the matrix contains anchored linear neutral polymers. The mean field theory of polymer solution is used to predict K, the partition coefficient of a polymer molecule distributing between the gel and mobile phases. The reduction in entropy suffered by the macromolecule in the gel phase is sufficient to produce an exponential dependence of K on the molecular weight of the partitioning species. The enthalpy of interaction between the gel polymer and the distributed species provides a parameter which describes the specificity or recognition in the interaction. The predicted linear dependence of in K on protein molecular weight is satisfactorily borne out by a data set on eight standard proteins chromatographed on four separate gel types.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

D E Brooks, W Müller. Size-exclusion phases and repulsive protein--polymer interaction/recognition.. https://doi.org/10.1002/(sici)1099-1352(199634%2F12)9%3A5%2F6%3C697%3A%3Aaid-jmr324%3E3.0.co%3B2-t

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Exactly solvable models of adaptive networks.

A satisfiability-unsatisfiability (SAT-UNSAT) transition takes place for many optimization problems when the number of constraints, graphically represented by links between variables nodes, is brought above some threshold. If the network of constraints is allowed to adapt by redistributing its links, the SAT-UNSAT transition may be delayed and preceded by an intermediate phase where the structure self-organizes to satisfy the constraints. We present an analytic approach, based on the recently introduced cavity method for large deviations, which exactly describes the two phase transitions delimiting this adaptive intermediate phase. We give explicit results for random bond models subject to the connectivity or rigidity percolation transitions, and compare them with numerical simulations.

Mathematical Computing↗

Surface-enhanced Raman spectroscopy and density functional theory study on 4,4'-bipyridine molecule.

The molecular geometry and vibrational frequencies of 4,4'-bipyridine (BPE) in the ground state were calculated using density functional theory (DFT) methods (B3LYP) with 6-31++G(d,p) basis set. The optimized geometric bond lengths and bond angles are obtained by DFT employing the hybrid of Beckes non-local three parameter exchange and correlation functional and Lee-Yang-Parr correlation functional. Fourier transform infrared (FT-IR), Fourier transform Raman (FT-Raman) and near-infrared surface-enhanced Raman scattering (NIR-SERS) spectra of BPE on the silver foil substrate have been recorded. All FT-IR, FT-Raman and NIR-SERS band were assigned on the basis of the B3LYP/6-31++G(d,p) method. The vibrational frequencies obtained by DFT(3LYP) are in good agreement with observed results. The NIR-SERS of BPE excited by 1064nm laser line is little difference with that excited by visible laser line. This phenomenon is result to the increase of the contribution of CHEM enhancement effect. Surface selection rules derived from the electromagnetic enhancement model were employed to infer the orientations of BPE on the silver foil substrate surface. Some vibrational frequency which are sensitive to the planar or non-planar structure of BPE, and to the dihedral angle were concluded.

Mathematical Computing↗