A novel 3D visualization approach: A proof-of-concept study on the histidine residues in myoglobin

We present a proof-of-concept study towards the development of a novel 3D visualization method, based on the existence in proteins — in addition to the extrinsic geometry — of two independent intrinsic geometric structures determined by the peptide planes and the side chains. The method makes use of the construction of a series of orthonormal coordinate frames along the protein side chains and mapping the atoms positions onto a unit sphere. We apply our method to analyze distal and proximal histidine residues in myoglobin. The results are in good agreement with biological data and provide a new perspective for further understanding of structure and function of histidine in myoglobin. This suggests the method can reliably depict the spatial orientation of side-chain covalent bonds in a protein and may eventually be advanced into a valuable visual tool for protein-structure prediction, validation and refinement, complementary to widely used visualization suits like VMD, Jmol, PyMOL and others.We present a proof-of-concept study towards the development of a novel 3D visualization method, based on the existence in proteins — in addition to the extrinsic geometry — of two independent intrinsic geometric structures determined by the peptide planes and the side chains. The method makes use of the construction of a series of orthonormal coordinate frames along the protein side chains and mapping the atoms positions onto a unit sphere. We apply our method to analyze distal and proximal histidine residues in myoglobin. The results are in good agreement with biological data and provide a new perspective for further understanding of structure and function of histidine in myoglobin. This suggests the method can reliably depict the spatial orientation of side-chain covalent bonds in a protein and may eventually be advanced into a valuable visual tool for protein-structure prediction, validation and refinement, complementary to widely used visualization suits like VMD, Jmol, PyMOL and others.

[1]  Jean-Paul Renaud,et al.  The role of the distal histidine in myoglobin and haemoglobin , 1988, Nature.

[2]  Xubiao Peng,et al.  A three dimensional visualisation approach to protein heavy-atom structure reconstruction , 2014, BMC Structural Biology.

[3]  Soumen Ghosh,et al.  Effect of curcumin on the binding of cationic, anionic and nonionic surfactants with myoglobin , 2017 .

[4]  Jing Du,et al.  The H93G Myoglobin Cavity Mutant as a Versatile Scaffold for Modeling Heme Iron Coordination Structures in Protein Active Sites and Their Characterization with Magnetic Circular Dichroism Spectroscopy. , 2011, Coordination chemistry reviews.

[5]  T. N. Bhat,et al.  The Protein Data Bank , 2000, Nucleic Acids Res..

[6]  M. Spivak A comprehensive introduction to differential geometry , 1979 .

[7]  Xu-biao Peng,et al.  Intrinsic protein geometry with application to non-proline cis peptide planes , 2018, Journal of Mathematical Chemistry.

[8]  Benno P. Schoenborn,et al.  Neutron diffraction reveals oxygen–histidine hydrogen bond in oxymyoglobin , 1981, Nature.

[9]  Jeffrey Skolnick,et al.  Fast procedure for reconstruction of full‐atom protein models from reduced representations , 2008, J. Comput. Chem..

[10]  Xu-biao Peng,et al.  Myoglobin ligand gate mechanism analysis by a novel 3D visualization technique , 2019, Journal of Mathematical Chemistry.

[11]  S. Nagao,et al.  Self-oxidation of cytochrome c at methionine80 with molecular oxygen induced by cleavage of the Met-heme iron bond. , 2014, Molecular bioSystems.

[12]  Yi Lu,et al.  Functional tuning and expanding of myoglobin by rational protein design , 2014, Science China Chemistry.

[13]  G. N. Ramachandran,et al.  Stereochemistry of polypeptide chain configurations. , 1963, Journal of molecular biology.

[14]  Yang Zhang,et al.  REMO: A new protocol to refine full atomic protein models from C‐alpha traces by optimizing hydrogen‐bonding networks , 2009, Proteins.