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Relational Systems Theory: An approach to complexity

Relational Systems Theory: An approach to complexity. Donald C. Mikulecky Professor Emeritus and Senior Fellow The Center for the Study of Biological Complexity. MY SORCES:. AHARON KATZIR-KATCHALSKY (died in massacre in Lod Airport 1972) LEONARDO PEUSNER (alive and well in Argentina)

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Relational Systems Theory: An approach to complexity

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  1. Relational Systems Theory: An approach to complexity Donald C. Mikulecky Professor Emeritus and Senior Fellow The Center for the Study of Biological Complexity

  2. MY SORCES: • AHARON KATZIR-KATCHALSKY (died in massacre in Lod Airport 1972) • LEONARDO PEUSNER (alive and well in Argentina) • ROBERT ROSEN (died December 29, 1998)

  3. ROUGH OUTLINE OF TALK • ROSEN’S COMPLEXITY • NETWORKS IN NATURE • THERMODYNAMICS OF OPEN SYSTEMS • THERMODYNAMIC NETWORKS • RELATIONAL NETWORKS • LIFE ITSELF

  4. COMPLEXITY • REQUIRES A CIRCLE OF IDEAS AND METHODS THAT DEPART RADICALLY FROM THOSE TAKEN AS AXIOMATIC FOR THE PAST 300 YEARS • OUR CURRENT SYSTEMS THEORY, INCLUDING ALL THAT IS TAKEN FROM PHYSICS OR PHYSICAL SCIENCE, DEALS EXCLUSIVELY WITH SIMPLE SYSTEMS OR MECHANISMS • COMPLEX AND SIMPLE SYSTEMS ARE DISJOINT CATEGORIES

  5. CAN WE DEFINE COMPLEXITY? Complexity is the property of a real world system that is manifest in the inability of any one formalism being adequate to capture all its properties. It requires that we find distinctly different ways of interacting with systems. Distinctly different in the sense that when we make successful models, the formal systems needed to describe each distinct aspect are NOT derivable from each other

  6. COMPLEX NO LARGEST MODEL WHOLE MORE THAN SUM OF PARTS CAUSAL RELATIONS RICH AND INTERTWINED GENERIC ANALYTIC  SYNTHETIC NON-FRAGMENTABLE NON-COMPUTABLE REAL WORLD SIMPLE LARGEST MODEL WHOLE IS SUM OF PARTS CAUSAL RELATIONS DISTINCT N0N-GENERIC ANALYTIC = SYNTHETIC FRAGMENTABLE COMPUTABLE FORMAL SYSTEM COMPLEX SYSTEMS VS SIMPLE MECHANISMS

  7. COMPLEXITY VS COMPLICATION • Von NEUMAN THOUGHT THAT A CRITICAL LEVEL OF “SYSTEM SIZE” WOULD “TRIGGER” THE ONSET OF “COMPLEXITY” (REALLY COMPLICATION) • COMPLEXITY IS MORE A FUNCTION OF SYSTEM QUALITIES RATHER THAN SIZE • COMPLEXITY RESULTS FROM BIFURCATIONS -NOT IN THE DYNAMICS, BUT IN THE DESCRIPTION! • THUS COMPLEX SYSTEMS REQUIRE THAT THEY BE ENCODED INTO MORE THAN ONE FORMAL SYSTEM IN ORDER TO BE MORE COMPLETELY UNDERSTOOD

  8. THERMODYNAMICS OF OPEN SYSTEMS • THE NATURE OF THERMODYNAMIC REASONING • HOW CAN LIFE FIGHT ENTROPY? • WHAT ARE THERMODYNAMIC NETWORKS?

  9. THE NATURE OF THERMODYNAMIC REASONING • THERMODYNAMICS IS ABOUT THOSE PROPERTIES OF SYSTEMS WHICH ARE TRUE INDEPENDENT OF MECHANISM • THEREFORE WE CAN NOT LEARN TO DISTINGUISH MECHANISMS BY THERMODYNAMIC REASONING

  10. SOME CONSEQUENCES • REDUCTIONISM DID SERIOUS DAMAGE TO THERMODYNAMICS • THERMODYNAMICS IS MORE IN HARMONY WITH TOPOLOGICAL MATHEMATICS THAN IT IS WITH ANALYTICAL MATHEMATICS • THUS TOPOLOGY AND NOT MOLECULAR STATISTICS IS THE FUNDAMENTAL TOOL

  11. EXAMPLES: • CAROTHEODRY’S PROOF OF THE SECOND LAW OF THERMODYNAMICS • THE PROOF OF TELLEGEN’S THEOREM AND THE QUASI-POWER THEOREM • THE PROOF OF “ONSAGER’S” RECIPROCITY THEOREM

  12. HOW CAN LIFE FIGHT ENTROPY? • DISSIPATION AND THE SECOND LAW OF THERMODYNAMICS • PHENOMENOLOGICAL DESCRIPTION OF A SYTEM • COUPLED PROCESSES • STATIONARY STATES AWAY FROM EQUILIBRIUM

  13. DISSIPATION AND THE SECOND LAW OF THERMODYNAMICS • ENTROPY MUST INCREASE IN A REAL PROCESS • IN A CLOSED SYSTEM THIS MEANS IT WILL ALWAYS GO TO EQUILIBRIUM • LIVING SYSTEMS ARE CLEARLY “SELF - ORGANIZING SYSTEMS” • HOW DO THEY REMAIN CONSISTENT WITH THIS LAW?

  14. PHENOMENOLOGICAL DESCRIPTION OF A SYTEM • WE CHOSE TO LOOK AT FLOWS “THROUGH” A STRUCTURE AND DIFFERENCES “ACROSS” THAT STRUCTURE (DRIVING FORCES) • EXAMPLES ARE DIFFUSION, BULK FLOW, CURRENT FLOW

  15. NETWORKS IN NATURE • NATURE EDITORIAL: VOL 234, DECEMBER 17, 1971, pp380-381 • “KATCHALSKY AND HIS COLLEAGUES SHOW, WITH EXAMPLES FROM MEMBRANE SYSTEMS, HOW THE TECHNIQUES DEVELOPED IN ENGINEERING SYSTEMS MIGHT BE APPLIED TO THE EXTREMELY HIGHLY CONNECTED AND INHOMOGENEOUS PATTERNS OF FORCES AND FLUXES WHICH ARE CHARACTERISTIC OF CELL BIOLOGY”

  16. A GENERALISATION FOR ALL LINEAR FLOW PROCESSES FLOW = CONDUCTANCE x FORCE FORCE = RESISTANCE x FLOW CONDUCTANCE = 1/RESISTANCE

  17. A SUMMARY OF ALL LINEAR FLOW PROCESSES

  18. COUPLED PROCESSES • KEDEM AND KATCHALSKY, LATE 1950’S • J1 = L11 X1 + L12 X2 • J2 = L21 X1 + L22 X2

  19. STATIONARY STATESAWAY FROM EQUILIBRIUMAND THE SECOND LAW OF THERMODYNAMICS • T Ds/dt = J1 X1 +J2 X2 > 0 • EITHER TERM CAN BE NEGATIVE IF THE OTHER IS POSITIVE AND OF GREATER MAGNITUDE • THUS COUPLING BETWEEN SYSTEMS ALLOWS THE GROWTH AND DEVELOPMENT OF SYSTEMS AS LONG AS THEY ARE OPEN!

  20. STATIONARY STATES AWAY FROM EQUILIBRIUM • LIKE A CIRCUIT • REQUIRE A CONSTANT SOURCE OF ENERGY • SEEM TO BE TIME INDEPENDENT • HAS A FLOW GOING THROUGH IT • SYSTEM WILL GO TO EQUILIBRIUM IF ISLOATED

  21. HOMEOSTASIS IS LIKE A STEADY STATE AWAY FROM EQUILIBRIUM

  22. IT HAS A CIRCUIT ANALOG J x L

  23. COUPLED PROCESSES • KEDEM AND KATCHALSKY, LATE 1950’S • J1 = L11 X1 + L12 X2 • J2 = L21 X1 + L22 X2

  24. THE RESTING CELL • High potassium • Low Sodium • Na/K ATPase pump • Resting potential about 90 - 120 mV • Osmotically balanced (constant volume)

  25. EQUILIBRIUM RESULTS FROM ISOLATING THE SYSTEM

  26. WHAT ARE THERMODYNAMIC NETWORKS? • ELECTRICAL NETWORKS ARE THERMODYNAMIC • MOST DYNAMIC PHYSIOLOGICAL PROCESSES ARE ANALOGS OF ELECTRICAL PROCESSES • COUPLED PROCESSES HAVE A NATURAL REPRESENTATION AS MULTI-PORT NETWORKS

  27. ELECTRICAL NETWORKS ARE THERMODYNAMIC • RESISTANCE IS ENERGY DISSIPATION (TURNING “GOOD” ENERGY TO HEAT IRREVERSIBLY - LIKE FRICTION) • CAPACITANCE IS ENERGY WHICH IS STORED WITHOUT DISSIPATION • INDUCTANCE IS ANOTHER FORM OF STORAGE

  28. A SUMMARY OF ALL LINEAR FLOW PROCESSES

  29. MOST DYNAMIC PHYSIOLOGICAL PROCESSES ARE ANALOGS OF ELECTRICAL PROCESSES L J C x

  30. C2 COUPLED PROCESSES HAVE A NATURAL REPRESENTATION AS MULTI-PORT NETWORKS J2 L J1 x2 C1 x1

  31. REACTION KINETICS AND THERMODYNAMIC NETWORKS • START WITH KINETIC DESRIPTION OF DYNAMICS • ENCODE AS A NETWORK • TWO POSSIBLE KINDS OF ENCODINGS AND THE REFERENCE STATE

  32. EXAMPLE: ATP SYNTHESIS IN MITOCHONDRIA EH+ <--------> [EH+] H+ [H+] E <-------------> [E] S P E MEMBRANE

  33. EXAMPLE: ATP SYNTHESIS IN MITOCHONDRIA-NETWORK I

  34. x2 x1 L22 IN THE REFERENCE STATE IT IS SIMPLY NETWORK II L22-L12 L11-L12 J2 J1

  35. THIS NETWORK IS THE CANNONICAL REPRESENTATION OF THE TWO FLOW/FORCE ENERGY CONVERSION PROCESS • ONSAGER’S THERMODYNAMICS WAS EXPRESSED IN AN AFFINE COORDINATE SYSTEM • THAT MEANS THERE CAN BE NO METRIC FOR COMPARING SYSTEMS ENERGETICALLY • BY EMBEDDING THE ONSAGER COORDINATES IN A HIGHER DIMENSIONAL SYSTEM, THERE IS AN ORTHOGANAL COORDINATE SYSTEM • IN THE ORTHOGANAL SYSTEM THERE IS A METRIC FOR COMPARING ALL SYSTEMS • THE VALUES OF THE RESISTORS IN THE NETWORK ARE THJE THREE ORTHOGONAL COORDINATES

  36. THE SAME KINETIC SYSTEM HAS AT LEAST TWO NETWORK REPRESENTATIONS, BOTH VALID • ONE CAPTURES THE UNCONSTRAINED BEHAVIOR OF THE SYSTEM AND IS GENERALLY NON-LINEAR • THE OTHER IS ONLY VALID WHEN THE SYSTEM IS CONSTRAINED (IN A REFERENCE STATE) AND IS THE USUAL THERMODYNAMIC DESRIPTION OF A COUPLED SYSTEM

  37. SR (BRIGGS,FEHER) GLOMERULUS (OKEN) ADIPOCYTE GLUCOSE TRANSPORT AND METABOLISM (MAY) FROG SKIN MODEL (HUF) TOAD BLADDER (MINZ) KIDNEY (FIDELMAN,WATTLINGTON) FOLATE METABOLISM (GOLDMAN, WHITE) ATP SYNTHETASE (CAPLAN, PIETROBON, AZZONE) SOME PUBLISHED NETWORK MODELS OF PHYSIOLOGICAL SYSTEMS

  38. Cell Membranes Become Network Elements in Tissue Membranes • Epithelia are tissue membranes made up of cells • Network Thermodynamics provides a way of modeling these composite membranes • Often more than one flow goes through the tissue

  39. An Epithelial Membrane in Cartoon Form:

  40. A Network Model of Coupled Salt and Volume Flow Through an Epithelium CL PL LUMEN AM TJ BL CELL BM BLOOD PB CB

  41. TELLEGEN’S THEOREM • BASED SOLEY ON NETWORK TOPOLOGY AND KIRCHHOFF’S LAWS • IS A POWER CONSERVATION THEOREM • STATES THAT VECTORS OF FLOWS AND FORCES ARE ORTHOGONAL. • TRUE FOR FLOWS AT ONE TIME AND FORCES AT ANOTHER AND VICE VERSA • TRUE FOR FLOWS IN ONE SYSTEM AND FORCES IN ANOTHER WITH SAME TOPOLOGY AND VICE VERSA

  42. RELATIONAL NETWORKS • THROW AWAY THE PHYSICS, KEEP THE ORGANIZATION • DYNAMICS BECOMES A MAPPING BETWEEN SETS • TIME IS IMPLICIT • USE FUNCTIONAL COMPONENTS-WHICH DO NOT MAP INTO ATOMS AND MOLECULES 1:1 AND WHICH ARE IRREDUCABLE

  43. LIFE ITSELF • CAN NOT BE CAPTURED BY ANY OF THESE FORMALISMS • CAN NOT BE CAPTURED BY ANY COMBINATION OF THESE FORMALISMS • THE RELATIONAL APPROACH CAPTURES SOME OF THE NON-COMPUTABLE, NON-ALGORITHMIC ASPECTS OF LIVING SYSTEMS

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