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Peptide Computing for NP-Complete Problems

This paper explores the use of peptide-antibody interactions to solve NP-Complete problems. It models gate and arithmetic operations using Binding-Blocking Automata.

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Peptide Computing for NP-Complete Problems

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  1. Computational Models using Peptide-Antibody Interactions M. Sakthi Balan and Kamala Krithivasan Theoretical Computer Science Lab Department of Computer Science and Engineering Indian Institute of Technology Madras Chennai – 600036.

  2. Organization • Peptide Computing • Objective of the Work • Solving NP-Complete problems • Modeling gate operations • Modeling arithmetic operations • Binding-Blocking Automata (BBA) • Normal-forms, Complexity measures of BBA • String Binding-Blocking Automata • Rewriting Binding-Blocking Automata • Conclusion

  3. Peptide Computing • Introduced by Hubert Hug and Rainer Schuler in 2000. • Solved satisfiability problem using peptide-antibody interactions.

  4. Peptide Computing • Uses peptides and antibodies • Operation – binding of antibodies to epitopes in peptides • Epitope – The site in peptide recognized by antibody • Highly non-deterministic • Massive parallelism

  5. Peptide ComputingContd.. • Peptides – sequence of amino acids • Twenty amino acids. Example – Glycine, Valine • Connected by covalent bonds

  6. Peptide ComputingContd.. • Antibodies recognizes epitopes by binding to it • Binding of antibodies to epitopes has associated power called affinity • Higher priority to the antibody with larger affinity power

  7. Objectives • Using peptide computing for solving NP-Complete problems. • To show this model is universal. • Modeling switching operations, arithmetical operations. • Defining automata model inspired by interactions between peptides and antibodies – Binding-Blocking Automata.

  8. Objectives (Contd..) • Analyze the power of Binding-Blocking Automata (BBA). • Define and study some complexity measures for BBA. • Define several variants of the model and study the acceptance power.

  9. Solving NP-Complete Problems

  10. Hamiltonian Path Problem • G = (V,E) is a directed graph • V = {v1,v2,…,vn} is the vertex set • E = {eij | vi is adjacent to vj} is the edge set • v1 - source vertex, vn – end vertex • Problem – Test whether there exists a Hamiltonian path between v1 and vn

  11. 1 3 2 4 5 6

  12. 1 3 2 4 5 6

  13. Peptides Formation • For each possible solution there is a peptide sequence formed. • Each of the pair of epitopes present in the peptide sequence denote a possible edge of the graph.

  14. Antibody Formation • Three sets of antibodies are formed. • One set to recognize all the legal edges. • One set to recognize all edges not present in the graph. • Last one to recognize the Hamiltonian path of the graph.

  15. Peptide Solution Space

  16. Algorithm • Take all the peptides in an aqueous solution • Add antibodies Aij • Add antibodies Bij • Add labeled antibody C • If fluorescence is detected answer is yes or else the answer is no

  17. Peptides with Antibodies

  18. Peptide with Antibodies

  19. labeled antibody

  20. Complexity • Number of peptides = (n-2)! • Length of peptides = O(n) • Number of antibodies =O(n2) • Number of Bio-steps is constant

  21. Exact Cover by 3-Sets Problem • Instance A finite set X = {x1,x2,…,xn}, n = 3q and a collection C of 3-elements subsets of X • Question: Does C contain an Exact Cover for X

  22. A Turing Machine can be simulated by a Peptide System Peptide Computing is Computationally Complete

  23. Universality Result • Turing machine, M = (Q, Σ, δ, s0, F) • Q = {q1,q2, … ,qm} • Σ = {a1,a2, …,al} • B is the blank symbol

  24. Universality ResultContd.. Peptide without antibodies

  25. Initial Configuration of Peptide

  26. Simulating the Right MoveContd..

  27. Complexity • Peptide system takes O(t(n)) time • Length of the peptide is O(s(n)) • Amount of antibodies is O(m.s(n)+l.(s(n))

  28. Switching Operations - OR, AND & NOT gates

  29. Why modeling gate operations? • Peptide and antibody formation is dependent on the problem. • Defining basic operations makes the model independent of the problem.

  30. Proposed Model • Consists of a peptide sequence and some set of antibodies. • Peptide sequence consists of five epitopes, • Six antibodies denoted by A1, A2, B1, B2, Cinit and Cf. • Antibodies A1, A2, B1 and B2 denote the inputs. • Cinit denote the initial value of the result of the operation. • Cinit and Cf denote the output of the operation.

  31. Proposed Model • Epitopes for the antibodies denoting the input to bind. • Epitope for the antibody representing the initial output to bind. • Epitopes for the antibodies denoting the output to bind.

  32. Peptide sequence Peptide Sequence with Antibodies

  33. OR Gate • Input bits 0 and 1 are represented by the antibodies Ai and Bi respectively where 1  i  2. • The antibody Cinit denotes the bit 0. • The antibody Cf(labeled antibody) denotes the bit 1. • epitope(A1) = {y}, epitope(A2) = {z}, • epitope(B1) = {yx1}, epitope(B2) = {x2z}, • epitope(Cinit) = {x1xx2}, epitope(Cf) = {x}, • aff(Bi) > aff(Cinit) > aff(Cf), 1  i  2.

  34. OR Gate • The output 1 occurs if at least one of the inputs is 1. • Start with an initial output of 0 - antibody Cinit binds to its epitope. • Cinit is toggled if at least one 1 comes as an input. For this to be carried out the epitopes for the antibody Cinit and the antibody Bi, 1  i  2 are taken as overlapping ones. • aff(Bi) > aff(Cinit) > aff(Cf), 1  i  2. • This facilitates toggle of output bit to 1 - antibody Cf binds to its epitope.

  35. Algorithm • Take the peptide sequence P in an aqueous solution. • Add the antibody C. • Add antibodies corresponding to the input bits. For example if the first bit is 1 and the second bit is 0 then add antibodies B1 and A2. • Add antibody Cf. If the output has to be seen the antibody Cf can be gives some color so that at the end of the algorithm if fluorescence is detected the output will be 1 or else it will be 0.

  36. Other Gates • This model has been extended to other gates – AND, NOT, NAND, NOR and XOR • We also extend this model to simulate Boolean circuits.

  37. Modeling Arithmetic Operations

  38. Arithmetic OperationsProposed Model • Consists of a peptide and set of antibodies • Peptide sequence has n position specific epitopes • Epitopes epi = yi xi zi, yiand zi are switching epitopes for the ithbit.

  39. y4 x4 z4 y0 x0 z0 Peptide Sequence for a 5-bit number

  40. Antibodies • A = {A0, A1, …, An-1} • B = {B0, B1, …, Bn-1} • TAB = {TAB0, TAB1, …, TAB(n-1)} • TBA = {TBA0, TBA1, …, TBA(n-1)}

  41. Binding Sites xizi yixi For Bi For Ai xi xi xizi > xi yixi > xi TABi Zi TBAi yi

  42. Affinity • aff(TABi) > aff(Ai) • aff(TBAi) > aff(Bi) • aff(TABi) = aff(TBAi)

  43. What it denotes? • Ai – denotes ith bit is zero • Bi – denotes ith bit is one • TABi – used to switch ith bit from zero to one • TBAi – used to switch ith bit from one to zero

  44. Representation of Binary Numbers • If the ith bit is 0 then the antibody Ai is bounded to the epitope yixi • If the ith bit is 1 then the antibody Bi is bounded to the epitope xizi

  45. Example B4 A3 B2 A1 B0 10101

  46. C = cn cn-1cn-2 …c0 Addition of Two Binary Numbers A = an-1an-2 …a0 B = bn-1bn-2 …b0

  47. ai bi Ci 1 0 0 0 2 0 1 1 3 1 0 1 4 1 1 0 XOR

  48. Addition (Contd..) • First step – guessing equivalent to XOR gate. • The bit cn is initialized to zero. • Carry propagation.

  49. Addition (Contd..) • Carry occurs only when both the bits aiand bi are 1. • Carry is propagated to the left until both the bits ajand bj (j > i) are 0. • If no such j exists then propagation stops making nth bit 1. • j.j-1….i+1 is called the carry block. • For each carry block j.j-1….i+1 invert the digits ck (i+1  k  j)

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