Skip to main content


Henry Koffler Distinguished Professor of Biological Sciences
  • 765-494-4956
  • HOCK 325

Associated website(s): Lab , PULSe , Publications


Structure/function of alpha-helical and beta-barrel membrane proteins involved in photosynthetic electron transport and energy transduction; structure-function of receptors involved in protein (specifically colicins) import.


Structure-Function of Membrane Proteins

Although there are more than 100,000 independent structures of soluble proteins in the Protein Data Bank, there are only approximately 500 such structures of integral membrane proteins in the PDB, and only a fraction are structures of hetero-oligomeric membrane proteins solved to a resolution ≤ 3.0 Å.  These membrane proteins are of great interest in health and disease-related studies.  In addition, they provide the major problem in understanding the assembly of membrane proteins.

A 2.5 Å structure has been obtained of the hetero-oligomeric cytochrome b 6 f complex, the electron and proton-transferring complex in photosynthetic electron transport (protein data bank deposition, PDB 4OGQ) The dimeric 250-kDa complex contains 8 polypeptide subunits, 13 trans-membrane helices, 7 prosthetic groups (4 hemes, 1 FeS cluster, 1 Chl a , 1 β-carotene), and 23 lipid binding sites per monomer. Such energy-transducing membrane proteins have the special property that their function can be studied by spectrophotometry. This property was used to determine that the dielectric constants between the 4 hemes in the dimer are heterogeneous, partly a consequence of integration of lipid in the protein.

Some problems of current interest are (i) further analysis of the role of lipid in stabilizing the b 6 f complex, (ii) effect of the trans-membrane electrical potential on the atomic structure, (iii) engineering the electron transport chain with a possible application to modifying the rate-limiting step of photosynthesis, (iv) understanding the mechanism of the elevated rate of superoxide production, (v) understanding the unique mechanism of redox-dependent cross-membrane information transfer in which oxidation of plastoquinol on one side of the membrane actives a kinase on the other side.

I. Photosynthetic Energy Transduction: Structure-Function of the Hetero-Oligomeric Membrane Lipoprotein, the Electron Transport Proton Translocating Cytochrome b 6 f Complex

Fig 1. Cytochrome b 6 f complex; electron transport pathway and site of superoxide generation. (A ) Trans-membrane quinol-mediated electron transfer pathway in dimeric cytochrome b 6 f complex, crystallized from cyanobacteria, showing site of superoxide generation on electro-chemically positive (p, lumen side) of the membrane. (B ) View of b 6 f complex along membrane normal, showing 26 trans-membrane helices, 2-fold symmetry axis, lipids and bound detergent. ( C ) p-side binding site of quinone analogue, tri-decyl-stigmatellin

II.  Hypothesis for trans-membrane (TM) signaling and activation of Stt7 kinase.

TM signaling involving a serine-threonine kinase (Stt7 in Chlamydomonas reinhardtii ) directs light energy distribution between the 2 photosystems of oxygenic photosynthesis.  Oxidation of plastoquinol mediated by the cyt b 6 f complex on the electrochemically positive (p) side of the thylakoid membrane, activates the kinase domain of Stt7 on the trans (negative (n)) side, leading to phosphorylation and redistribution (“state transition”) of the light-harvesting chlorophyll proteins between the 2 photosystems. Stt7 kinase was cloned, expressed, and purified, (a) found to be active in vitro in the presence of reductant, and (b) purified as a tetramer, determined by analytical ultracentrifugation, EM, and electrospray-ionization mass spectrometry, with a molecular weight of 332 kDa, consisting of an 83.41 k. (c) Far-UV circular dichroism spectra showed Stt7 to be mostly α-helical, and document a physical interaction with the b 6 f complex. O 2 •- , generated in the b 6 f complex via plastosemiquinone, proposed to reduce S-S bond between 2 Cys in Stt7, causing a conformation change in the Stt7 TM domain, which is transmitted to the n-side through a proline hinge in TM domain, thus activating the kinase. In cartoon mode, p-side domain containing Cys 68 and 73 shown as blue oval, TM domain as brown cylinders, and the proline hinge as a gray ( A ) and yellow ( B ) pentagon. n-side Stt7 kinase domain shown in gray in inactive state D (labeled A ) and, when activated, as red rectangle E (labeled B ) C-terminal disordered domain, orange rectangle. Cyt b 6 f complex (PDB ID 4H13) shown in surface representation, with the p-side plastoquinol (Q p ) binding site marked by the quinol-analog tridecyl stigmatellin (purple sticks). Lipid bilayer, light green. ( A ) Q p -site of cyt b 6 f complex unoccupied, cysteines 68 and 73 of Stt7 form disulfide bond, and kinase remains inactive. ( B ) Upon binding and oxidation of plastoquinol at the Q p -site, PQ •- is generated which, serving as reductant for O 2 , generating O 2 •- , is oxidized to PQ.

III. Structure-Function of Integral Membrane Proteins: (ll) β-barrel proteins, protein import, the colicin translocon

Like many bacteriophage, for their import into the bacterial cell, colicins parasitize outer membrane proteins normally used for uptake of metabolites (e. g., sugars, metals, vitamins).

Hypotheses for the pathway and mechanisms of import into E. coli of the cytotoxic E colicins are based on crystal structures of the colicins, and of complexes of the colicins with their outer membrane receptors, for example, the vitamin B12 receptor (BtuB), [panels A, B ] which the colicins parasitize for import. (A) 1.95 Å structure of the BtuB vitamin B 12 receptor ( J. Mol. Biol, 364, 716, 2006). (B) (side view) . (C) A 2.75 Å structure of the complex of receptor-binding domain of the endoribonucleolytic colicin E3 showed its elongate 100 Å long colicin domain to be bound obliquely, in which it appears to be 'fishing' for a second outer membrane receptor-translocator ( Nature Struct. Biol. , 10, 948-, 2003) (D) . A similar structure has been obtained with the receptor-binding domain of colicin E2 (Sharma et al ., JBC , 2007).

Single molecule fluorescence studies show a rapid diffusion of the colicin-BtuB receptor complex in the outer membrane as it diffuses rapidly in the outer membrane ( Biophys. J. , 99: 3880-3886, 2010) and searches for its outer membrane OmpF translocator protein in what has been described as a “fishing pole” mechanism. Thus, colicin import across the outer membrane involves formation of a ‘ Translocon ' between BtuB and OmpF.  A 3.0 Å crystal structure was obtained of a complex between the translocation domain of colicin E3 and OmpF, and 1.6 Å of OmpF alone ( EMBO J. , 27, 2171, 2008), and summarized in recent reviews: (1) Annual Reviews of Genetics , 46, 209-231, 2012); most recently On Mechanisms of Colicin Import: the Outer Membrane Quandary , Biochem. J., 475, 3903-3915. 2018.

Applications of these approaches and concepts to membrane-mediated action of proteins involved in infectious diseases: ( a ) The membrane-mediated interaction of the alpha-synuclein protein, implicated in the etiology of Parkinson’s Disease, in which the 140 residue disordered polypeptide was found to assume a significantly ordered helical structure upon binding to anionic liposome membranes ( Biochemistry , 46:14369-14379). ( b ) Application of the cytotoxic action of colicins to the problem of antibiotic bacteria (W. A. Cramer and L. N. Csonka),


B. S., Physics, Massachusetts Institute of Technology
Ph. D., Biophysics, University of Chicago
Postdoctoral, University of California/San Diego


Outside Lecture-Seminar Invitations (2019-2021)

  • Symposium, 100 Years of Cytochromes , American Chemical Society, Division of Biological Chemistry, San Francisco, August 16, 2020; to be held in Spring, 2021
  • Conference on Regulation of Photosynthesis , Kobe, Japan, 9-13 Nov. 2020; Lecture on “Structure-Function of the Cytochrome b6f Complex”; postponed to 2021
  • 3 rd Annual Congress on Plant Science and Biosecurity , July 06-08, 2020, Osaka, Japan; Lecture on Structure-Function of the Cytochrome b 6 f Comple x; now postponed or cancelled
  • 11 th European Workshop on the Biology of Cyanobacteria, scheduled for Porto, Portugal, 6-10, September 2020; held on-line; Lecture on “Structure-Function of the Cyanobacterial Cytochrome b6f Complex”
  • Annual Mtg. Biophysical Society, Baltimore, March, 2019; (1) Co-Chair, Biophysical Society Symposium, “Trans-membrane Signaling,” Lecture, “Redox-Dependent Trans-membrane signaling; (2) Co-Chair, Bioenergetics Sub-group Symposium on “Super-Complexes in Electron Transport;” Lecture, “Redox-Dependent Trans-membrane Signaling in the Cytochrome b6f Complex”

Outside Lecture-Seminar Invitations (2011-2019)

  • Orton K. Stark Distinguished Lectures, Miami University, April 18-20, 2017. "Structure-Function of the Cytochrome b6f Lipoprotein Complex; Interaction with the Trans-Membrane Stt7 Ser-Thr Kinase that Mediates State Transitions; Keynote Lecture, 26th Western Photosynthesis Conf., Pt. Reyes, CA, Jan 5-8, 2017.
  • Redox-Dependent Trans-Membrane Signaling in Photosynthetic State Transitions: Interaction of a Serine-Threonine Kinase with the Cytochrome b 6 f Complex,” 7 th International    Conference, Photosynthesis Research for Sustainability,Pushchino, Moscow Region, June   19-26, 2016.
  • "A Potential Problem with the Accuracy of Membrane Protein Structures”, NIH                Roadmap/Argonne National Laboratory Meeting on Membrane Protein Structures, April 11,    2015
  • “Mapping the Dielectric Heterogeneity of the Cytochrome b 6 f Membrane Lipoprotein Complex,” Symposium on Membrane Proteins, University of Delaware, Newark, Delaware, May 12, 2014.
  • “Structure-Function of Two Membrane Proteins: Helical and β-Barrel,” Dept. of Chemistry and Biochemistry, North Dakota State University, Fargo, ND, April 3, 2014.
  • "Mapping of the Heterogenous Dielectric Constant of the Cytochrome b 6 f Complex," Biophysics Seminar Series, Dept. of Cellular and Molecular Biology, UC Davis, Davis, CA, March 7, 2014.
  • "Mapping of the Heterogenous Dielectric Constant of the Cytochrome b 6f Complex," Department of Chemistry & Biochemistry, UCLA, Los Angeles, CA, February 20, 2014.
  • "Dielectric Heterogeneity in the Cytochrome b 6f Complex," Annual Meeting of the German Society of Biochemistry and Molecular Biology, Frankfurt, Germany, October 3, 2013.
  • "Dielectric Heterogeneity in the Cytochrome b 6 f Complex," International Congress of Photosynthesis, St. Louis, MO, August 12 – 15, 2013.
  • “Properties of the Hetero-Oligomeric Cytochrome b 6 f -Lipidic Charge Transfer Complex of Oxygenic Photosynthesis,” Department of Molecular Biology, University of Geneva, Geneva, Switzerland, June 17, 2013.
  • “Transfer of electrons, Protons, and Information in the Cytochrome b 6 f Lipidic Complex of Oxygenic Photosynthesis,” NIH Roadmap Meeting to Membrane Protein Technologies, University of California, San Francisco, CA, November 27-30, 2012.
  • “Lipid Functions in Cytochrome bc Complexes: an unusual event in evolution,” Conference, “How bugs kill bugs, progress and challenges in bacteriocin research,” British Biochemical Society, Nottingham, England. July 16 – 18, 2012.
  • "Lipid Functions in cytochrome bc complexes: an unusual event in evolution," Membrane Conference, Arizona State University, Phoenix, AZ, May 13-17, 2012.
  • “Lipid Functions in cytochrome bc complexes: an unusual event in evolution,” Royal Society Center, Chicheley Buckinghamshire, UK, May 3, 2012.
  • “The Cytochrome b 6 f Complex: an Odd Lipid Effect in Evolution; An Electrostatically Constrained Electron Transport Pathway,” May 3 – 4, 2012. Royal Society Discussion on “Structure and Dynamics of the Thylakoid Membrane,” Kavi Royal Society International Centre, Buckinghamshire, UK.
  • "Structure-Function (Energetic) of Hetero-Oligomeric Membrane Protein Complexes;" Symposium on "Structure-Function of Hetero-Oligomeric Membrane Proteins," Bioenergetics Subgroup, Biophysical Society, San Diego, California, February 25, 2012.
  • "Impediments in Travel through Membrane Proteins: Problems in Bioenergetics and Protein Import;" February 13, 2012. Department of Biochemistry and Biophysics, University of Stockholm, Sweden.
  • “Oligomeric Membrane Protein Complexes;" Symposium on "Structure-Function of Hetero-Oligomeric Membrane Proteins," February 25, 2012. Bioenergetics Subgroup, Biophysical Society, San Diego, CA.
  • "Traveling Inside the Cytochrome bc Complex of Energy-Transducing Membranes," January 5, 2012. Department of Biophysics, Albert Einstein College of Medicine, Bronx, NY.
  • Seminar: “Structure-Function of Cytochrome bf Complex,” December 5, 2011, the Biophysics and Computational Biology Department, University of Illinois-Champaign/Urbana.
  • Invited talk: “On the rate limiting step in photosynthetic electron transport,” November 4, 2011,
  • Conference on Natural and Artificial Photosynthesis, Renssalaer Polytechnic Institute, Troy, NY.
  • “Travels on and Within Membrane Proteins,” September 29, - October 1, 2011, the Department of Chemistry, University of Missouri.
  • Lawrence Berkeley National Lab BioEnergy, Photo- and Bio- Chemistry Site Visit, July 24-26, 2011, Univ. of California/Berkeley, CA.
  • “Impediments in traveling through membrane proteins: problems in bioenergetics and protein import.” March 31, 2011, Dept. of Biochemistry & Molecular Biology, Rosalind Franklin University of Medicine and Science, North Chicago, IL.
  • Panel Member at the organization meeting of the X-ray free electron laser. January 18 – 21, 2011, University of California/Berkeley, Berkeley, CA.


National Science Foundation Postdoctoral Fellowship, Univ. Calif/San Diego 1965-67;

NIH(NIGMS) Research Career Development Award, 1970-75;

Senior Fellow, European Molecular Biology Org., Univ. of Amsterdam, The Netherlands, 1974-75;

McCoy Award, Purdue University, Achievements in Science, 1988;

Plenary Lectures, International Congress of Photosynthesis, 1989, 2004;

Fellow, Alexander von Humboldt Foundation, 1992;

Fellow, John Simon Guggenheim Foundation, 1992-93;

C.F. Kettering Award, Amer. Soc. Plant Physiology, 1996;

Rosetta Briegel Barton Lecture, University of Oklahoma, 2001;

Maurice Hilleman Lecture, Montana State University, 2004;

Daniel Arnon Lecture, University of California/Berkeley, 2006;

Fellow, Biophysical Society, 2007;

Eminent Scholar Lecture, Oklahoma State University, 2008.

Orton K. Stark Lectures, Miami University, 2017

Fellow, American Association for the Advancement of Science, 2017

Orton K. Stark Distinguished Lectures, Miami University, 2017

Keynote Awardee, 9th International Conference on Photosynthesis & Hydrogen Energy Research for Sustainability, Hyderabad, India, 2017

American Chemical Society, Symposium, “One Hundred Years of Cytochromes,” San Francisco, now virtual, 2020

Purdue University Biological Sciences, 915 W. State Street, West Lafayette, IN 47907

Main Office: (765) 494-4408   Business Office: (765) 494-4764  Contact Us

© 2020 Purdue University | An equal access/equal opportunity university | Copyright Complaints

Trouble with this page? Disability-related accessibility issue? Please contact the College of Science Webmaster.

Maintained by Science IT