Importance of R-CF3···O Tetrel Bonding Interactions in Biological Systems.

In this article, ab initio calculations have been combined with a search in the Protein Data Bank (PDB) to demonstrate the importance of σ-hole tetrel bonding interactions in biological systems. In particular, we focus our attention on the ability of the -CF3 group to participate in noncovalent interactions as Lewis acids, and we show the importance of this interaction in the inhibition mechanism of a NADP+-dependent isocitrate dehydrogenase (IDH) enzyme that converts isocitrate to α-ketoglutarate. IDH mutations are found in multiple hematologic and solid tumors, inducing premalignant disorders. A potent triazine-based inhibitor of the mutant IDH (enasidenib) presents two -CF3 groups in the structure. One establishes a tetrel bonding interaction with an aspartate residue that contributes to the binding and selectivity of the inhibitor to the active site.

[1]  A. P. Davis,et al.  Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors , 2015, Angewandte Chemie.

[2]  Antonio Bauzá,et al.  Tetrel-bonding interaction: rediscovered supramolecular force? , 2013, Angewandte Chemie.

[3]  Timothy Clark,et al.  Halogen bonding and other σ-hole interactions: a perspective. , 2013, Physical chemistry chemical physics : PCCP.

[4]  Timothy Clark,et al.  σ-Holes: σ-Holes , 2013 .

[5]  D. Quiñonero,et al.  Cation–π and anion–π interactions , 2011 .

[6]  M. Luo,et al.  An NADPH Sensor Protein (HSCARG) Down-regulates Nitric Oxide Synthesis by Association with Argininosuccinate Synthetase and Is Essential for Epithelial Cell Viability* , 2008, Journal of Biological Chemistry.

[7]  Antonio Bauzá,et al.  The bright future of unconventional σ/π-hole interactions. , 2015, Chemphyschem : a European journal of chemical physics and physical chemistry.

[8]  Hans W. Horn,et al.  ELECTRONIC STRUCTURE CALCULATIONS ON WORKSTATION COMPUTERS: THE PROGRAM SYSTEM TURBOMOLE , 1989 .

[9]  Timothy Clark,et al.  Directional Weak Intermolecular Interactions: σ-Hole Bonding , 2010 .

[10]  Hua Yang,et al.  AG-221, a First-in-Class Therapy Targeting Acute Myeloid Leukemia Harboring Oncogenic IDH2 Mutations. , 2017, Cancer discovery.

[11]  Donald G. Truhlar,et al.  Systematic study of basis set superposition errors in the calculated interaction energy of two HF molecules , 1985 .

[12]  Timothy Clark,et al.  Halogen bonding: an electrostatically-driven highly directional noncovalent interaction. , 2010, Physical chemistry chemical physics : PCCP.

[13]  E. Arunan,et al.  The X-C···Y (X = O/F, Y = O/S/F/Cl/Br/N/P) 'carbon bond' and hydrophobic interactions. , 2013, Physical chemistry chemical physics : PCCP.

[14]  Pierangelo Metrangolo,et al.  Halogen bonding based recognition processes: a world parallel to hydrogen bonding. , 2005, Accounts of chemical research.

[15]  A. Frontera,et al.  Competition between Halogen Bonding and π-Hole Interactions Involving Various Donors: The Role of Dispersion Effects. , 2015, Chemphyschem : a European journal of chemical physics and physical chemistry.

[16]  Peter Murray-Rust,et al.  Angular preferences of intermolecular forces around halogen centers: preferred directions of approach of electrophiles and nucleophiles around carbon-halogen bond , 1986 .

[17]  H. Schaefer,et al.  Extensive theoretical studies of the hydrogen‐bonded complexes (H2O)2, (H2O)2H+, (HF)2, (HF)2H+, F2H−, and (NH3)2 , 1986 .

[18]  A. Frontera,et al.  Putting anion-π interactions into perspective. , 2011, Angewandte Chemie.

[19]  Peter Politzer,et al.  Expansion of the σ-hole concept , 2009, Journal of molecular modeling.

[20]  Peter Politzer,et al.  Halogen bonding: an interim discussion. , 2013, Chemphyschem : a European journal of chemical physics and physical chemistry.

[21]  Peter Murray-Rust,et al.  Computer retrieval and analysis of molecular geometry. 4. Intermolecular interactions , 1979 .

[22]  S. Leutwyler,et al.  An ab initio benchmark study of hydrogen bonded formamide dimers. , 2006, The journal of physical chemistry. A.

[23]  A. Frontera,et al.  1,1,2,2-Tetracyanocyclopropane (TCCP) as supramolecular synthon. , 2016, Physical chemistry chemical physics : PCCP.

[24]  S. J. Grabowski Tetrel bond-σ-hole bond as a preliminary stage of the SN2 reaction. , 2014, Physical chemistry chemical physics : PCCP.

[25]  A. Galano,et al.  Counterpoise corrected interaction energies are not systematically better than uncorrected ones: comparison with CCSD(T) CBS extrapolated values , 2010 .

[26]  J. Elguero,et al.  Cooperativity in Tetrel Bonds. , 2016, The journal of physical chemistry. A.

[27]  A. Frontera,et al.  Small cycloalkane (CN)2C-C(CN)2 structures are highly directional non-covalent carbon-bond donors. , 2014, Chemistry.

[28]  A. Frontera,et al.  Tetrel Bonding Interactions. , 2016, Chemical record.

[29]  T. N. Guru Row,et al.  Experimental evidence for 'carbon bonding' in the solid state from charge density analysis. , 2014, Chemical Communications.

[30]  T. Dunning,et al.  A Road Map for the Calculation of Molecular Binding Energies , 2000 .

[31]  G. Reifenberger,et al.  IDH1(R132H) mutation increases murine haematopoietic progenitors and alters epigenetics , 2012, Nature.

[32]  S. Lowe,et al.  Cancer-associated IDH2 mutants drive an acute myeloid leukemia that is susceptible to Brd4 inhibition , 2013, Genes & development.

[33]  Antonio Bauzá,et al.  σ-Hole Opposite to a Lone Pair: Unconventional Pnicogen Bonding Interactions between ZF3 (Z=N, P, As, and Sb) Compounds and Several Donors. , 2016, Chemphyschem : a European journal of chemical physics and physical chemistry.

[34]  S. Amani,et al.  Effect of cooperativity in lithium bonding on the strength of halogen bonding and tetrel bonding: (LiCN)n···ClYF3 and (LiCN)n···YF3Cl (Y= C, Si and n = 1–5) complexes as a working model , 2015, Journal of Molecular Modeling.

[35]  M. Luo,et al.  NADPH is an allosteric regulator of HSCARG. , 2009, Journal of molecular biology.

[36]  P. Pandolfi,et al.  Proto-oncogenic role of mutant IDH2 in leukemia initiation and maintenance. , 2014, Cell stem cell.

[37]  A. Frontera,et al.  RCH3···O Interactions in Biological Systems: Are They Trifurcated H-Bonds or Noncovalent Carbon Bonds? , 2016 .

[38]  Jean-Philip Piquemal,et al.  NCIPLOT: a program for plotting non-covalent interaction regions. , 2011, Journal of chemical theory and computation.

[39]  Hans-Jörg Schneider,et al.  Binding mechanisms in supramolecular complexes. , 2009, Angewandte Chemie.

[40]  Peter Murray-Rust,et al.  Intermolecular interactions of the carbon-fluorine bond: the crystallographic environment of fluorinated carboxylic acids and related structures , 1983 .

[41]  P. Ballester,et al.  Nature of noncovalent carbon-bonding interactions derived from experimental charge-density analysis. , 2015, Chemphyschem : a European journal of chemical physics and physical chemistry.

[42]  M. Luo,et al.  Restructuring of the dinucleotide-binding fold in an NADP(H) sensor protein , 2007, Proceedings of the National Academy of Sciences.

[43]  J. Murray,et al.  Trends in σ-hole strengths and interactions of F3MX molecules (M = C, Si, Ge and X = F, Cl, Br, I) , 2013, Journal of Molecular Modeling.

[44]  Qingzhong Li,et al.  Competition and cooperativity between tetrel bond and chalcogen bond in complexes involving F2CX (X = Se and Te) , 2015 .