26.12.2014 Views

Clinical Biochemistry of Domestic Animals (Sixth Edition) - UMK ...

Clinical Biochemistry of Domestic Animals (Sixth Edition) - UMK ...

Clinical Biochemistry of Domestic Animals (Sixth Edition) - UMK ...

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Chapter 5<br />

Proteins, Proteomics, and the<br />

Dysproteinemias<br />

P. David Eckersall<br />

Division <strong>of</strong> Animal Production & Public Health<br />

Institute <strong>of</strong> Comparative Medicine<br />

University <strong>of</strong> Glasgow<br />

Glasgow, Scotland<br />

United Kingdom<br />

I. INTRODUCTION<br />

II. CLASSIFICATION OF PROTEINS<br />

A. Structural Classification<br />

B. Chemical Classification<br />

C. Physical Classification<br />

III. METABOLISM OF PROTEINS<br />

A. General<br />

B. Synthesis <strong>of</strong> Proteins<br />

C. Catabolism <strong>of</strong> Proteins<br />

IV. PLASMA PROTEINS<br />

A. Sites <strong>of</strong> Synthesis<br />

B. Functions <strong>of</strong> the Plasma Proteins<br />

C. Factors Influencing the Plasma Proteins<br />

D. Handling and Identification <strong>of</strong> Proteins<br />

V. METHODOLOGY<br />

A. Total Protein<br />

B. Fractionation <strong>of</strong> the Serum Proteins<br />

C. Electrophoretic Fractionation <strong>of</strong> the Serum Proteins<br />

D. Specific Protein Analysis<br />

VI. NORMAL PLASMA AND SERUM PROTEINS<br />

A. Albumin<br />

B. Acute Phase Proteins<br />

C. Complement Proteins<br />

D. Immunoglobulins<br />

E. Lipoproteins<br />

F. Other Serum Proteins<br />

G. Multiplex Assays, Protein Arrays, and Acute Phase<br />

Index<br />

VII. INTERPRETATION OF SERUM PROTEIN<br />

PROFILES<br />

A. Physiological Influences<br />

B. The Dysproteinemias<br />

REFERENCES<br />

I . INTRODUCTION<br />

Protein is the most abundant component <strong>of</strong> plasma. There<br />

is in the region <strong>of</strong> 6 to 7 g/dl (60 to 70 g/liter) <strong>of</strong> protein<br />

in plasma in comparison to 0.1 g/dl (1.0 g/liter) <strong>of</strong> glucose<br />

(5.5 mmol/liter) or 0.35 g/dl (3.50 g/liter) <strong>of</strong> sodium<br />

(150 mmol/liter). However, this large mass <strong>of</strong> protein<br />

consists <strong>of</strong> many different individual protein molecules.<br />

Complete analysis <strong>of</strong> this complex mixture <strong>of</strong> different<br />

proteins is not possible at present in the diagnostic laboratory.<br />

Proteins contain approximately 95% <strong>of</strong> all nitrogenous<br />

material in blood in the form <strong>of</strong> chains <strong>of</strong> amino acids<br />

linked by peptide bonds. Protein can be separated from the<br />

nonprotein nitrogen (NPN) component <strong>of</strong> plasma by precipitation<br />

with reagents such as trichloracetic acid. The<br />

NPN consists <strong>of</strong> nucleic acids along with low molecular<br />

weight compounds such as urea (50% <strong>of</strong> NPN), free amino<br />

acids (25% <strong>of</strong> NPN), glutathione, and creatinine.<br />

Analysis <strong>of</strong> serum protein is an area <strong>of</strong> clinical biochemistry<br />

<strong>of</strong> domestic animals, which has seen a rapid advance<br />

since the 1990s, and with current developments in analytical<br />

technology and interpretation, the rate <strong>of</strong> advance is<br />

likely to accelerate rather than decline. At the forefront <strong>of</strong><br />

these advances in the diagnostic application <strong>of</strong> serum protein<br />

analysis has been the development <strong>of</strong> specific assays<br />

for individual proteins. In particular, it has been recognized<br />

that quantification <strong>of</strong> a group <strong>of</strong> serum protein called the<br />

acute phase proteins (APP) can greatly assist the assessment<br />

<strong>of</strong> infection, inflammation, and trauma in animals. These<br />

advances are now being applied in clinical biochemistry laboratories<br />

for the immediate benefit in the diagnosis, prognosis,<br />

and monitoring <strong>of</strong> treatment <strong>of</strong> domestic animals.<br />

In the future, technology may be developed to characterize<br />

all proteins (the proteome) <strong>of</strong> serum, which would<br />

<strong>Clinical</strong> <strong>Biochemistry</strong> <strong>of</strong> <strong>Domestic</strong> <strong>Animals</strong>, 6th <strong>Edition</strong> 117<br />

Copyright © 2008, Elsevier Inc.<br />

All rights reserved.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!