What are the key reactions of lysine in biochemistry. How does lysine interact with various chemical agents. Why is lysine’s reactivity important for protein modification and analysis.

The Nucleophilic Nature of Lysine’s Side Chain

Lysine is a versatile amino acid with a highly reactive side chain. Its ε-amino group acts as a potent nucleophile, enabling it to participate in various chemical reactions. This reactivity makes lysine a crucial target for protein modifications and a valuable tool in biochemical analysis.

Why is lysine so reactive?

The reactivity of lysine stems from its side chain structure. At physiological pH, the ε-amino group of lysine is typically protonated, carrying a positive charge. However, when the pH is raised above lysine’s pKa (around 10.5), the amino group becomes deprotonated. In this state, the lone pair of electrons on the nitrogen atom makes it a powerful nucleophile, ready to attack electrophilic centers in various molecules.

Acylation Reactions of Lysine

One of the most common reactions involving lysine is acylation, where the amino group acts as a nucleophile to attack carbonyl compounds.

How does lysine react with anhydrides?

Lysine readily reacts with anhydrides in a nucleophilic substitution reaction, also known as acylation. The ε-amino group of lysine attacks one of the carbonyl carbons of the anhydride, leading to the formation of an amide bond and the release of a carboxylic acid.

A specific example of this type of reaction is lysine’s interaction with methylmaleic anhydride (also called citraconic anhydride). This reaction is reversible, allowing for temporary modification of lysine residues in proteins.

Formation of Amidine and Guanidine Derivatives

Lysine can participate in reactions that modify its amino group to form more complex nitrogen-containing functional groups.

What happens when lysine reacts with ethylacetimidate?

Lysine reacts with high specificity and yield toward ethylacetimidate in a nucleophilic substitution reaction. Ethylacetimidate is similar to ethyl acetate, but with an imido group replacing the carbonyl oxygen. In this reaction, ethanol is expelled as the amidino group forms. The resulting amidine structure contains two nitrogen atoms attached to the central carbon.

How does lysine form guanidino groups?

Lysine can react with O-methylisourea in a nucleophilic substitution reaction. This process involves the expulsion of methanol and results in the formation of a guanidino group. A guanidino group is characterized by three nitrogen atoms attached to a central carbon atom.

Lysine’s Role in Protein Labeling and Analysis

The reactivity of lysine’s amino group makes it an excellent target for protein labeling and analysis techniques.

Which reagents are commonly used to label lysine residues?

Several reagents are employed to specifically label lysine residues in proteins:

• Fluorodinitrobenzene (FDNB), also known as Sanger’s reagent
• Trinitrobenzenesulfonate (TNBS)
• Dimethylaminonapthelenesulfonylchloride (Dansyl Chloride)

These reagents react with lysine in nucleophilic aromatic substitution reactions, forming stable derivatives that can be easily detected and analyzed.

What is the significance of these labeling reactions?

Labeling lysine residues serves several purposes in biochemistry and protein science:

1. Protein sequencing: Labeled lysine residues help determine the position of lysines in a protein’s primary structure.
2. Quantification: The number of lysine residues in a protein can be determined by measuring the extent of labeling.
3. Structural studies: Labeled lysines can provide information about protein folding and surface accessibility.
4. Protein modification: Selective labeling of lysines can alter protein properties or introduce new functionalities.

Lysine’s Reaction with Aldehydes: Formation of Imines

Lysine exhibits high specificity in its reaction with aldehydes, forming a class of compounds known as imines or Schiff bases.

How do imines form from lysine and aldehydes?

The reaction between lysine and aldehydes involves the nucleophilic attack of the ε-amino group on the carbonyl carbon of the aldehyde. This results in the formation of an unstable intermediate called a carbinolamine, which then undergoes dehydration to form the imine (Schiff base). The reaction is reversible under physiological conditions.

Can these imines be further modified?

Yes, the imines formed from lysine and aldehydes can be further modified. One common modification is reduction, which can be achieved using sodium borohydride or cyanoborohydride. This reduction converts the imine to a more stable secondary amine, effectively “locking” the modification in place.

Biological Significance of Lysine Reactions

The diverse reactivity of lysine plays crucial roles in various biological processes and has significant implications for protein function and regulation.

How do lysine modifications affect protein function?

Lysine modifications can impact protein function in several ways:

• Altering enzyme activity: Modification of lysine residues in or near active sites can change enzyme catalytic properties.
• Regulating protein-protein interactions: Lysine modifications can create or disrupt binding sites for other proteins.
• Influencing protein stability: Some modifications can affect protein folding or resistance to degradation.
• Modulating cellular localization: Certain lysine modifications act as signals for protein trafficking within cells.

What are some examples of biologically important lysine modifications?

Several lysine modifications play critical roles in cellular processes:

1. Acetylation: Involved in histone modification and gene regulation.
2. Methylation: Also important in histone modification and epigenetic control.
3. Ubiquitination: Tags proteins for degradation or alters their function.
4. SUMOylation: Regulates protein-protein interactions and cellular localization.
5. Glycation: Non-enzymatic modification that can occur in diabetes and aging.

Applications of Lysine Chemistry in Biotechnology

The unique reactivity of lysine has been harnessed for various biotechnological applications.

How is lysine chemistry used in protein engineering?

Protein engineers exploit lysine’s reactivity to introduce new functionalities into proteins:

• Bioconjugation: Attaching small molecules, polymers, or other proteins to lysine residues.
• Cross-linking: Creating covalent bonds between proteins or within a single protein.
• PEGylation: Attaching polyethylene glycol chains to improve protein stability and pharmacokinetics.
• Immobilization: Anchoring proteins to solid supports for various applications.

What role does lysine play in drug development?

Lysine chemistry is valuable in several aspects of drug development:

1. Antibody-drug conjugates: Lysine residues are often used to attach cytotoxic drugs to antibodies for targeted cancer therapy.
2. Prodrug design: Lysine-based modifications can be used to improve drug solubility or targeting.
3. Enzyme inhibitors: Understanding lysine reactivity helps in designing inhibitors that target lysine-dependent enzymes.
4. Peptide synthesis: Lysine’s side chain protection and deprotection are crucial in solid-phase peptide synthesis.

Analytical Techniques Exploiting Lysine Reactivity

The unique chemical properties of lysine make it a valuable target for various analytical techniques in protein science.

How is lysine used in protein quantification methods?

Lysine’s reactivity is exploited in several protein quantification techniques:

• TNBS assay: Measures free amino groups, primarily from lysine residues.
• Fluorescamine assay: Reacts with primary amines to form fluorescent products.
• OPA (o-phthaldialdehyde) assay: Forms fluorescent derivatives with lysine and other primary amines.

What role does lysine play in mass spectrometry-based proteomics?

Lysine is crucial in several aspects of mass spectrometry-based proteomics:

1. Trypsin digestion: Trypsin cleaves proteins after lysine and arginine residues, generating peptides suitable for MS analysis.
2. Isotope labeling: Methods like SILAC (Stable Isotope Labeling by Amino acids in Cell culture) often use isotopically labeled lysine for quantitative proteomics.
3. Cross-linking studies: Lysine-specific cross-linkers are used to probe protein-protein interactions and protein structure.
4. Post-translational modification analysis: Many important PTMs occur on lysine residues and can be detected and quantified by MS.

Understanding the diverse chemistry of lysine is essential for biochemists, protein engineers, and anyone working in the field of protein science. Its reactivity makes it a powerful tool for protein modification, analysis, and engineering, while also playing crucial roles in cellular processes through various post-translational modifications. As our knowledge of lysine chemistry continues to expand, so too will our ability to manipulate and understand proteins in ever more sophisticated ways.

2.1.5: A5. Reactions of Lysine

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• Henry Jakubowski
• College of St. Benedict/St. John’s University

• reacts with anhydride in a nucleophilic substitution reaction (acylation).
• reacts reversibly with methylmaleic anhydride (also called citraconic anhydride) in a nucleophilic substitution reaction.
• reacts with high specificity and yield toward ethylacetimidate in a nucleophilic substitution reaction (ethylacetimidate is like ethylacetate only with a imido group replacing the carbonyl oxygen). Ethanol leaves as the amidino group forms. (has two N -i.e. din – attached to the C)

Figure: LYSINE REACTIONS 2

• reacts with O-methylisourea in a nucleophilic substitution reaction. with the expulsion of methanol to form a guanidino group (has 3 N attached to C, nidi)
• reacts with fluorodintirobenzene (FDNB or Sanger’s reagent) or trinitrobenzenesulfonate (TNBS, as we saw with the reaction with phosphatidylethanolamine) in a nucleophilic aromatic substitution reaction to form 2,4-DNP-lysine or TNB-lysine.
• reacts with Dimethylaminonapthelenesulfonylchloride (Dansyl Chloride) in a nucleophilic substitution reaction.

Figure: LYSINE REACTIONS 3

• reacts with high specificity toward aldehydes to form imines (Schiff bases), which can be reduced with sodium borohydride or cyanoborohydride to form a secondary amine.

• Prof. Henry Jakubowski (College of St. Benedict/St. John’s University)

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Reactions of Lysine



Reactions of Lysine

BIOCHEMISTRY – DR. JAKUBOWSKI

Last Update: 
02/27/16

•  reacts with anhydride in a nucleophilic substitution reaction
  (acylation).
• reacts reversibly with methylmaleic anhydride (also called
  citraconic anhydride) in a nucleophilic substitution reaction.
• reacts with high specificity and yield toward ethylacetimidate in a
  nucleophilic substitution reaction (ethylacetimidate  is like
  ethylacetate only with a imido group replacing the carbonyl oxygen).
  Ethanol leaves as the amidino group forms. (has two N -i.e. din –
  attached to the C)

Figure:  LYSINE REACTIONS 2

• reacts with O-methylisourea in a nucleophilic substitution reaction.
  with the expulsion of methanol to form a guanidino group (has 3 N
  attached to C, nidi)
• reacts with fluorodintirobenzene (FDNB or Sanger’s reagent) or
  trinitrobenzenesulfonate (TNBS, as we saw with the reaction with
  phosphatidylethanolamine) in a nucleophilic aromatic substitution
  reaction to form 2,4-DNP-lysine or TNB-lysine.
• reacts with Dimethylaminonapthelenesulfonylchloride
  (Dansyl Chloride) in a nucleophilic substitution reaction.

Figure:  LYSINE REACTIONS 3

• reacts with high specificity toward aldehydes to form imines (Schiff
  bases), which can be reduced with sodium borohydride or cyanoborohydride
  to form a secondary amine.

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Argumentation of symptomatic therapy of acute tonsillopharyngitis | Morozova S.V.

Diagnosis and treatment of acute infectious and inflammatory diseases of the pharynx is one of the main problems solved by practical otorhinolaryngology. The pharynx, located at the junction of the respiratory and digestive tracts, is subject to the action of numerous damaging factors that can disrupt the protective and adaptive reactions and the functioning of the mucous membrane and the lymphoid apparatus of the pharynx.

The reasons contributing to the occurrence of pharyngeal pathological changes are numerous and varied: exposure to an infectious agent, diseases of the gastrointestinal tract (GIT), diseases of the teeth and periodontium, smoking, adverse environmental, professional and domestic factors, diet errors, trauma.
It is important to note the medical and social significance of the problem. Thus, acute respiratory viral diseases, the annual incidence of which is up to 8 people per 1,000 population, are accompanied by inflammation in the respiratory tract affecting the pharynx [4]. A high level of morbidity leads to a large number of outpatient visits of the working population and students, an increase in the level of temporary disability both in the number of cases and in the number of days missed due to illness and care, to significant expenses for the purchase of medicines – within the family budget and significant financial losses – on a national scale.
Undoubtedly, one of the most common diseases of the pharynx is acute tonsillopharyngitis, which is confirmed by the high level of morbidity and the appeal of patients to general practitioners and otorhinolaryngologists. In the implementation of the disease, the leading role belongs to the infectious factor (viruses, bacteria, fungi) with a significant predominance of viruses (adenoviruses, rhinoviruses, coronaviruses, influenza viruses, parainfluenza viruses, Coxsackie A viruses, etc.). According to modern domestic scientific and clinical studies, which allow a clear idea of ​​the nature and sensitivity of the key bacterial pathogens of acute infectious and inflammatory diseases of the pharynx (microorganisms isolated with a clinically significant degree of contamination over 104 CFU / ml), the leading role is played by Streptococcus pyogenes. In patients with bacterial tonsillitis, the inoculation of group A β-hemolytic streptococcus (GABHS) reaches 80–100%, less often group C and G streptococci, Corynebacterium diphtheriae, Neisseria gonorrhoeae, Arcanobacterium haemolyticum are isolated [4, 7].
In the practice of a doctor, it is necessary to take into account the importance of identifying acute “streptococcal” tonsillopharyngitis, when the disease has a severe, protracted course, there are cases of systemic inflammatory response syndrome (SIRS). With tonsillopharyngitis caused by GABHS, there is a high probability of developing severe complications and life-threatening conditions, such as meningitis, pneumonia, sepsis, toxic shock syndrome, rheumatic fever, post-streptococcal glomerulonephritis, etc.
In acute “streptococcal” tonsillopharyngitis, the most likely routes of infection are contact and airborne. The reservoir is, as a rule, a sick person or a carrier; colonization of the pathogen is possible on the skin, mucous membrane of the pharynx and nasal cavity. An alimentary route of infection is possible – with improper storage of food, in particular dairy products. Predisposing factors for the onset of the disease are local and general hypothermia, a decrease in general and local immunity, and sometimes mechanical trauma to the tonsils.
The disease is characterized by a sudden onset, intense sore throat, most pronounced when swallowing, a feeling of dryness, soreness, sore throat, moderate (febrile) fever, headache. Patients note general weakness, malaise, loss of appetite, aching pain in the limbs. The “tonsillar” lymph nodes enlarge and become painful on palpation. With pharyngoscopy, a bright diffuse reddening of the mucous membrane of the pharynx is determined, changes in the palatine tonsils may correspond to one of the forms of primary (vulgar) tonsillitis: the palatine tonsils are enlarged, edematous and hyperemic (catarrhal tonsillitis), yellowish-white plaques are visible on the surface of the palatine tonsils (lacunar tonsillitis). ), festering follicles in the form of small yellowish vesicles (follicular tonsillitis).
The McIsaac scale helps to determine the degree of probability of streptococcal etiology of acute tonsillopharyngitis at the first stage of assessing the patient’s condition, based on the clinical manifestations of the disease. Analysis and quantitative (scoring) assessment of such criteria as fever, cough, condition of the cervical lymph nodes, palatine tonsils, patient’s age allow, with a high degree of probability, to assess the risk of streptococcal infection and determine the tactics of treatment and diagnostic measures [8]. At the same time, patients with infectious and inflammatory diseases of the pharynx, of course, need a multifaceted examination, including, in particular, such informative studies as bacteriological and immunological, which makes it possible to fully diagnose both the disease and the diagnosis of the patient. It should be recognized that in modern conditions, laboratory information is extremely important for high-quality clinical diagnostics [3].
The bacteriological method is the isolation of a pure culture of the pathogen and its identification, determination of its sensitivity to antibiotics and other chemotherapeutic drugs. Both the classical culture method by inoculation and express methods for identifying group A streptococci are used: immunochromatographic rapid test for GABHS antigens in throat swabs, methods for detecting pathogen antigens (enzyme-linked immunosorbent assay and direct immunofluorescence), methods for detecting pathogen DNA (polymerase chain reaction ), which are characterized by high sensitivity and absolute specificity.
Immunological examination allows diagnosing primary and secondary immunological deficiency. Secondary (acquired) immunological deficiency – damage to the initially unchanged immune system under the influence of various exogenous factors (infections, tumors, renal failure, long-term use of glucocorticosteroids, cytostatics). Primary (congenital) immunological deficiency is much less common – the inability of the body to implement one or another link of the immune response due to a genetically determined defect or impaired development of the lymphoid system in ontogenesis.
Diagnostics involves carrying out tests of the 1st level, which include the determination of the absolute and relative number of lymphocytes, T- and B-lymphocytes, the level of serum lg (IgM, IgG, IgA), phagocytic activity of leukocytes, as well as tests of the 2nd level: determination regulatory subpopulations (T-helpers, T-suppressors), interleukin-producing activity of cells, assessment of the proliferative activity of T- and B-lymphocytes in the reaction of blast transformation, killer activity of lymphocytes, identification of immune complexes, etc.
An important stage in the diagnosis of acute tonsillopharyngitis is differential diagnosis with diseases that have a similar symptom complex (infectious mononucleosis, diphtheria). Children’s respiratory tract infections (scarlet fever, measles) are accompanied by catarrhal oropharyngeal changes. Changes in the pharyngeal mucosa in diseases of the gastrointestinal tract (chronic gastritis, peptic ulcer, oral dysbacteriosis, gastroesophageal reflux disease, cholecystitis, pancreatitis) are very common [2].
Often, the initial and determining factor, subjectively regarded as a state of ill health, which forces patients to seek medical help, is the occurrence and severity of pain when swallowing, as well as soreness, perspiration, dry paroxysmal cough. Among the extremely numerous and diverse causes of sore throat (neuralgia of the glossopharyngeal nerve, spinal diseases, cardiovascular diseases (angina pectoris, myocardial infarction), thyroiditis, injuries and foreign bodies of the pharynx and esophagus, mental disorders, AIDS, oropharyngeal cancer, etc. ) tonsillopharyngitis is one of the most common etiological factors [6, 11].
The appearance of acute pain in the throat performs a signal function in case of inflammation of the pharynx, indicates the presence of a damaging factor, initiates protective-compensatory-adaptive processes in the body, therefore, in relation to acute tonsillopharyngitis, the expression that has become a popular expression is quite appropriate: “Pain is the watchdog of health.” However, with a sharp intensity and duration of pain, overstrain occurs, the patient develops a negative psycho-emotional state, he experiences painful anguish, and there is a clear motivation to eliminate pain as an extremely negative sensation. Pain disrupts the vital activity of the human body, inevitably affects the quality of life – an indicator directly related to the state of health, from the category of positive factors goes into the category of negative ones and needs to be eliminated [1, 5]. Pain sensations are characterized by a wide range of individual fluctuations. According to the severity of pain in acute infectious and inflammatory diseases of the pharynx, patients largely judge the severity of the disease and expect from the therapy, first of all, complete relief from pain.
These factors cannot be ignored when assessing the patient’s condition, developing therapeutic tactics and determining the effectiveness of the therapy. In this case, 2 main approaches are used: assessing the intensity of pain (“how much the patient suffers”) and assessing the impact of pain on well-being in general (“psychological state, quality of life”) [13]. Scales for the subjective assessment of the severity of pain by the patient at the time of the study are widely used in clinical practice: a visual analogue scale of pain, as well as a digital rating scale that has a number of advantages, consisting of 11 points, where 0 means no pain, 10 means pain that cannot be tolerated [ 15].
In the treatment of acute infectious and inflammatory diseases of the pharynx, drugs with antimicrobial, anti-inflammatory, analgesic, immunocorrective effects are currently used: antibacterial drugs, topical immunocorrective vaccine preparations, local antiseptics, decongestants, and hyposensitizing drugs [7]. In the complex of therapeutic measures for diseases of the pharynx, accompanied by pain, fever, an important role belongs to drugs that have a symptomatic therapeutic effect. Timely and adequate symptomatic therapy for acute tonsillopharyngitis is no less important than etiopathogenetic treatment, since its goals are to reduce the severity and eliminate the clinical manifestations of the disease, which have a significant negative impact on the patient’s daily life, to preserve his ability to perform household activities and social activity.
One of the most commonly used groups of drugs with analgesic, antipyretic and anti-inflammatory effects is non-steroidal anti-inflammatory drugs (NSAIDs). The appearance of pain during inflammatory processes is associated with the formation of prostaglandins at the site of inflammation, which irritate pain receptors and cause the appearance of a subjective sensation – pain. The principle of the analgesic action of NSAIDs is based on the suppression of the activity of cyclooxygenase types 1 and 2 (COX-1, COX-2) – the main enzymes necessary for the formation of prostaglandins.
A representative of this group is the drug OKI (lysine salt of ketoprofen). The drug has anti-bradykinin activity, stabilizes lysosomal membranes and delays the release of enzymes from them that contribute to tissue destruction in chronic inflammation, reduces the release of cytokines, and inhibits the activity of neutrophils. The lysine salt of Ketoprofen has anti-inflammatory, analgesic and antipyretic effects. The rapid onset of action is due to the higher solubility of the lysine salt of ketoprofen than that of unchanged ketoprofen, faster and more complete absorption of the active substance, which leads to the peak of its plasma concentration when taken orally after 15 minutes. The effect of the drug appears after 15-20 minutes. and persists for several hours, while unchanged ketoprofen reaches a maximum only after 60 minutes. after admission [12].
The OKI preparation is convenient to use, since it has various forms of release: granules for the preparation of a solution for oral administration, rectal suppositories (for the symptomatic treatment of inflammatory processes accompanied by fever and pain), and a topical solution (for the symptomatic treatment of inflammatory oropharyngeal diseases) . For oral administration, adults and children over 14 years of age, the contents of one two-volume sachet (full dose – 80 mg) should be dissolved in half a glass of drinking water and taken 3 times a day with meals. Children 6-14 years old and elderly patients are recommended to use the contents of 1/2 two-volume sachet (half the dose – 40 mg). Rectally, children aged 6–12 years are prescribed 1 suppository of OKI 60 mg 1–2 r./day; children over 12 years old – up to 3 rubles / day. Adults are prescribed 1 suppository of OKI 160 mg 2–3 rubles / day (elderly patients – no more than 2 suppositories / day). Locally, the drug is used in the form of a rinse solution, using in adults for 1 rinse 10 ml (5 injections) of an OKI solution, previously diluted with drinking water using the glass attached to the package. Adolescents over 12 years of age should use no more than 6 ml (3 injections) of the OKI solution for 1 rinse. The procedure must be carried out 2 rubles / day.
Contraindications to the use of the drug OKI are the “aspirin triad”, hypersensitivity to NSAIDs. The drug is also contraindicated for systemic use during exacerbation of peptic ulcer and ulcerative colitis, Crohn’s disease, diverticulitis, blood clotting disorders, severe renal dysfunction, in children under 6 years of age, in the third trimester of pregnancy and during lactation.
The analgesic effect of AEI is based on a triple mechanism: peripheral – through blockade of the arachidonic acid cycle, central – due to a decrease in the sensitivity of brain receptors and due to blockade of impulse transmission in the spinal cord. Comparative studies have shown that the analgesic efficacy of OCI is higher and manifests itself faster than that of ibuprofen and paracetamol [14]. The antipyretic effect of OCI is comparable to that of paracetamol and is more pronounced than that of ibuprofen and other NSAIDs [9]. According to the anti-inflammatory effect, OKI demonstrates high activity, significantly exceeding the activity of nimesulide [10]. Taking into account the fact that the use of nimesulide is limited in Europe, OKI as a lysine salt of ketoprofen is a worthy alternative to nimesulide, which minimizes the risk of developing adverse events from the liver.
An important aspect of the use of drugs for symptomatic therapy is their safety and tolerability. When prescribing NSAID therapy, special attention is paid to the undesirable effects inherent in the drugs of this group, primarily from the gastrointestinal tract and the hematopoietic system. Abdominal pain, diarrhea, exacerbation of gastritis or peptic ulcer, hepatic reactions – this is not a complete list of possible adverse events. In this aspect, the lysine salt of ketoprofen has advantages over ketoprofen, since it causes side effects much less frequently. Due to its chemical composition, OKI quickly mixes with a neutral pH environment and, due to this, has almost no irritating effect on the gastrointestinal mucosa. According to L. Bellussi et al. (1996), against the background of a 10-day intake of the OCI drug, the overall tolerability of therapy by patients and gastroscopy data were comparable with those when taking placebo [10].
To achieve the desired effect of pharmacotherapy, a patient with acute infectious and inflammatory diseases of the pharynx must follow the following basic recommendations: completely give up smoking and alcohol; exclude hot, cold, spicy, salty foods and drinks from the diet; in the absence of contraindications, conduct warming and distracting physiotherapy procedures at home.
Thus, the rational use of drugs for symptomatic therapy allows not only to achieve a positive clinical effect in the treatment of acute inflammatory diseases of the pharynx, but also to increase the level of patient satisfaction with the results of treatment.

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2. Vesyaeva A.A. Treatment of chronic pharyngitis associated with pathology of the gastrointestinal tract: Proceedings of the XVII Congress of Otorhinolaryngologists of Russia, Nizhny Novgorod, June 2006, pp. 165–166.
3. Menshikov V.V. (ed.), Dedov I.I., Makolkin V.I., Mukhin N.A. Clinical diagnosis – laboratory basis. M.: Labinform, 1997. 304 p.
4. Kolobukhina L.V. Viral infections of the respiratory tract // RMJ, 2000. V. 8. No. 13-14 (114-115). pp. 559–564.
5. Lerish R. Fundamentals of physiological surgery. Essays on the vegetative life of tissues / transl. from French B.M. Nikiforova M.: Medgiz, 1961. 292 p.
6. Morozova S.V. Pain in the throat: causes and possibilities of drug therapy // BC. 2005. V. 13. No. 21. S. 1447–1452.
7. Ryazantsev S.V. Etiopathogenetic therapy of acute pharyngitis: Method. recommendations. St. Petersburg: St. Petersburg Research Institute of Ear, Throat, Nose and Speech, 2008.
8. Shpynev K.V., Krechikov V.A. Modern approaches to the diagnosis of streptococcal pharyngitis // KMAH. 2007. V. 9. No. 1. S. 20–33.
9. D’Arienzo M. Summary of product characteristics // Drugs Exptl.Clin.Res. 1984 Vol. X(12) . R. 863–866.
10. Bellussi L. et al. Antiphlogistic therapy with ketoprofen lysine salt vs nimesulide in secretory otitis media, rhinitis/rhinosinusitis, pharyngitis/tonsillitis/tracheitis // Note di Terapia Otorinolaringol. 1996 Vol. 46. ​​R. 49–57.
11. Denk-Linnet D.-M., Mancusi G. Current diagnostics of swallowing disorders: the ENT specialists and phoniatricians role // European Archives of Oto-Rhino-Laringology and Head & Neck. June 2007 Vol. 264. Suppl. 1. HIC 5. R. 6.
12. Fatti F. Summary of product characteristics. Data on file, 1991.
13. Haefeli M., Elfering A., Aebi M. et al. What constitutes a good outcome in spinal surgery? A preliminary survey among spine surgeons of the SSE and European spine patients // Eur Spine J. 2008. 17. P. 104–116.
14. Ligniere G.C. et al. Ricenti Progressi in Medicina, II Pensiero Scientifico Editore. 1996 Vol. 87 (supplemento al #3).
15. Wewers M.E., Lowe N.K. A critical review of visual analogue scales in the measurement of clinical phenomena // Res Nurs Health. 1990 Vol. 13. R. 227–236.

Faculty of Biology St. Petersburg State University